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        <title>Annals of Hematology via MedWorm.com</title>
        <description>MedWorm.com provides a medical RSS filtering service. Over 6000 RSS medical sources are combined and output via different filters. This feed contains the latest items from the 'Annals of Hematology' source.</description>
        <link><![CDATA[http://www.medworm.com/rss/search.php?qu=Annals+of+Hematology&t=Annals+of+Hematology&s=Search&f=source]]></link>
        <lastBuildDate>Wed, 08 Feb 2012 17:41:56 +0100</lastBuildDate>
        <item>
            <title>Nine years interval between first and second bone marrow transplantations and subsequent long-term survival—a case of acute myeloid leukemia with MLL-AF6 fusion gene</title>
            <link>http://www.medworm.com/index.php?rid=5668115&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ft0524q54235q000m%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorPages 1-3DOI 10.1007/s00277-012-1417-2Authors
		Yasuhisa Yokoyama, Department of Hematology, Faculty of Medicine, University of Tsukuba, 1-1-1, Tennodai, Tsukuba, Ibaraki, JapanKazumi Suzukawa, Department of Hematology, Faculty of Medicine, University of Tsukuba, 1-1-1, Tennodai, Tsukuba, Ibaraki, JapanYasushi Okoshi, Department of Hematology, Faculty of Medicine, University of Tsukuba, 1-1-1, Tennodai, Tsukuba, Ibaraki, JapanToru Nanmoku, Department of Clinical Laboratory, Tsukuba University Hospital, Tsukuba, Ibaraki, JapanNaoshi Obara, Department of Hematology, Faculty of Medicine, University of Tsukuba, 1-1-1, Tennodai, Tsukuba, Ibaraki, JapanTerukazu Enami, Department of Hematology, Faculty of Medicine, University of Tsukuba, ...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5668115</comments>
            <pubDate>Fri, 03 Feb 2012 17:12:41 +0100</pubDate>
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        <item>
            <title>Kinetics of blood CD34+ cells after chemotherapy plus G-CSF in poor mobilizers: Implications for pre-emptive plerixafor use</title>
            <link>http://www.medworm.com/index.php?rid=5668116&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F03646h275m108721%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Mobilization and collection of stem cells is difficult in a proportion of patients intended for autologous stem cell transplantation
 (ASCT). We have evaluated mobilization kinetics of blood CD34+ cells (B-CD34+) to form basis for algorithm to facilitate rational pre-emptive plerixafor use. Altogether 390 chemomobilized patients were
 included. Forty-three patients (11%) did not reach B-CD34+ count ≥10 × 106/l. Mobilization kinetics differed according to the mobilization capacity observed. Among those who were very poor or inadequate
 mobilizers (peak B-CD34+ count ≤5 × 106/l and 6–10 × 106/l, respectively), B-CD34+ counts rarely rose after white blood cells (WBC) &amp;gt;5–10 × 109/l, whereas in many standard mobilizers a later rise in CD34+ cou...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5668116</comments>
            <pubDate>Thu, 02 Feb 2012 18:15:06 +0100</pubDate>
            <guid isPermaLink="false">5668116</guid>        </item>
        <item>
            <title>Primary MALT lymphoma of the urinary bladder in the background of interstitial cystitis</title>
            <link>http://www.medworm.com/index.php?rid=5668117&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh2j7577372w7r833%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorPages 1-2DOI 10.1007/s00277-012-1419-0Authors
		Ken Morita, Department of Hematology and Oncology, Graduate School of Medicine, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-8655 JapanFumihiko Nakamura, Department of Hematology and Oncology, Graduate School of Medicine, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-8655 JapanYasuhito Nannya, Department of Hematology and Oncology, Graduate School of Medicine, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-8655 JapanAkira Nomiya, Department of Urology, Graduate School of Medicine, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-8655 JapanShunya Arai, Department of Hematology and Oncology, Graduate School of Medicine, The University...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5668117</comments>
            <pubDate>Thu, 02 Feb 2012 06:56:37 +0100</pubDate>
            <guid isPermaLink="false">5668117</guid>        </item>
        <item>
            <title>Features of extramedullary myeloma relapse: high proliferation, minimal marrow involvement, adverse cytogenetics: a retrospective single-center study of 24 cases</title>
            <link>http://www.medworm.com/index.php?rid=5649296&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ff0318lh12421142r%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Extramedullary (e) relapse in multiple myeloma (MM) has an adverse prognosis, but knowledge concerning biological features
 and preferred treatment is scarce. We screened the myeloma registry of our institution for eMM relapses and identified 24
 cases among 357 patients (pts). Only 8% of eMM relapses occurred after initial therapy, but 54% occurred after third-line
 or subsequent therapy. Baseline molecular cytogenetics revealed high-risk features in 10 of 19 evaluable patients. Most frequently,
 eMM presented as soft tissue (67%) and organ involvement (25%) or malignant effusion (12.5%). Incidence of leptomeningeal/CNS
 involvement was 21%. At eMM relapse, bone marrow infiltration was absent in 46% and low in 21%. Ten eMM biopsies were available
 showing increased pro...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5649296</comments>
            <pubDate>Mon, 30 Jan 2012 06:32:07 +0100</pubDate>
            <guid isPermaLink="false">5649296</guid>        </item>
        <item>
            <title>Serum ferritin levels and endocrinopathy in medically treated patients with β thalassemia major</title>
            <link>http://www.medworm.com/index.php?rid=5649298&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ff152218uj3421578%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The association between iron overload indices and pathology of the heart and liver in transfusion-dependent patients with
 β thalassemia major (TM) has been extensively studied. Nonetheless, data on endocrine disease remains limited. This was a
 cross-sectional study of 382 TM patients treated with regular transfusions and desferrioxamine at the Thalassemia Center in
 Dubai, UAE. Retrieved data included demographics, splenectomy status, steady-state serum ferritin levels, and the presence
 of endocrinopathies (diabetes mellitus, hypothyroidism, hypoparathyroidism, and hypogonadism). Multivariate logistic regression
 analyses were used to determine which variables were independently associated with the occurrence of each endocrinopathy.
 The mean age of patients was 15....</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5649298</comments>
            <pubDate>Fri, 27 Jan 2012 06:53:43 +0100</pubDate>
            <guid isPermaLink="false">5649298</guid>        </item>
        <item>
            <title>Clinical features and prognostic factors of Asian patients with paroxysmal nocturnal hemoglobinuria: results from a single center in China</title>
            <link>http://www.medworm.com/index.php?rid=5649297&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp775008183w714qm%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Although all patients with paroxysmal nocturnal hemoglobinuria (PNH) have acquired mutations in the phosphatidylinositol glycan
 class-A(PIG-A)gene, their clinical courses are highly variable. We reviewed 280 PNH cases referred to our hospital from January
 1990 through June 2010 to assess clinical presentations, prognostic factors influencing survival, difference among subcategories,
 and clinical significance of PNH clone size. The overall survival at 10&amp;nbsp;years after diagnosis estimated by Kaplan–Meier was
 77.6%. Both univariate and multivariate analyses identified risk factors affecting survival, including age &amp;gt;40&amp;nbsp;years, absolute
 neutrophil count&amp;lt;0.5 × 109 cells/L, development of thrombotic events, evolution to myelodysplastic syndrome or acut...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5649297</comments>
            <pubDate>Fri, 27 Jan 2012 06:53:43 +0100</pubDate>
            <guid isPermaLink="false">5649297</guid>        </item>
        <item>
            <title>Rituximab pharmacokinetics in ascites and serum in the treatment of follicular lymphoma with massive ascites</title>
            <link>http://www.medworm.com/index.php?rid=5649299&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn04p64083wpqx7wm%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorPages 1-2DOI 10.1007/s00277-012-1410-9Authors
		Yuki Hiroshima, Third Department of Internal Medicine, Yamagata University School of Medicine, 2-2-2, Iidanishi, Yamagata-shi, Yamagata, 990-9585 JapanKatsushi Tajima, Third Department of Internal Medicine, Yamagata University School of Medicine, 2-2-2, Iidanishi, Yamagata-shi, Yamagata, 990-9585 JapanYousuke Shiono, Third Department of Internal Medicine, Yamagata University School of Medicine, 2-2-2, Iidanishi, Yamagata-shi, Yamagata, 990-9585 JapanIkuko Suzuki, Third Department of Internal Medicine, Yamagata University School of Medicine, 2-2-2, Iidanishi, Yamagata-shi, Yamagata, 990-9585 JapanKei Kouno, Third Department of Internal Medicine, Yamagata University School of Medicine, ...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5649299</comments>
            <pubDate>Fri, 27 Jan 2012 06:53:41 +0100</pubDate>
            <guid isPermaLink="false">5649299</guid>        </item>
        <item>
            <title>Analysis of hepatitis B surface antibody titers in B cell lymphoma patients after rituximab therapy</title>
            <link>http://www.medworm.com/index.php?rid=5639125&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F9033818jlp262132%2F</link>
            <description>In conclusion, we found that anti-HBs titers decreased significantly (P &amp;lt; 0.001) after rituximab treatment. B cell lymphoma patients with low pre-treatment anti-HBs titers (&amp;lt;100&amp;nbsp;mIU/mL) were more
 likely to lose anti-HBs antibodies and were at risk of HBV reactivation after rituximab immunochemotherapy.
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-6DOI 10.1007/s00277-012-1405-6Authors
		Sung-Nan Pei, Division of Hema-Oncology, Department of Internal Medicine, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine, Kaohsiung, TaiwanMing-Chun Ma, Division of Hema-Oncology, Department of Internal Medicine, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine, Kaohsiung, TaiwanMing-Chung Wang, Div...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5639125</comments>
            <pubDate>Tue, 24 Jan 2012 12:25:51 +0100</pubDate>
            <guid isPermaLink="false">5639125</guid>        </item>
        <item>
            <title>Unstable hemoglobin Rush [beta 101(G3) Glu&gt;Gln, HBB:c.304G&gt;C] in a Brazilian family with moderate hemolytic anemia</title>
            <link>http://www.medworm.com/index.php?rid=5639127&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ff077gt11833p7481%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Hemoglobin Rush is an unstable variant generated by a mutation of the β-globin gene which causes amino acid replacement Glu&amp;gt;Gln
 in the central cavity of hemoglobin (G3). Many members of a Brazilian family of Italian descent have hemoglobin Rush. This
 is the second report in world literature. Clinical and laboratory features were retrieved and gene mutation was characterized.
 Hemoglobin electrophoresis, gene sequencing, and restriction fragment length polymorphism with Hpy188I were used to characterize
 it. In 13 affected members, hemoglobin ranged from 9.3 to 13.0&amp;nbsp;g/dL and reticulocyte count up to 12.8%. The intensity of hemolysis
 appeared to be linked to increased stress. The mutation was proved to be HBB:c.304G&amp;gt;C, beta 101(G3) Glu&amp;gt;Gln. Heterozygous
...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5639127</comments>
            <pubDate>Tue, 24 Jan 2012 12:25:50 +0100</pubDate>
            <guid isPermaLink="false">5639127</guid>        </item>
        <item>
            <title>Falciparum malaria in a patient with sickle cell trait with hemophagocytosis and secondary pancytopenia</title>
            <link>http://www.medworm.com/index.php?rid=5639126&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp71v078l56414126%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorPages 1-2DOI 10.1007/s00277-012-1408-3Authors
		Jalil Ur Rehman, Department of Oncology, King Faisal Specialist Hospital and Research Centre, Po Box 40047, Jeddah, 21499 Kingdom of Saudi ArabiaNezar Bhabri, Department of Medicine, King Faisal Specialist Hospital and Research Centre, Jeddah, Kingdom of Saudi ArabiaAhmed Waleed, Department of Medicine, King Faisal Specialist Hospital and Research Centre, Jeddah, Kingdom of Saudi ArabiaA. Maulawi, Department of Pathology, King Faisal Specialist Hospital and Research Centre, Jeddah, Kingdom of Saudi ArabiaM. Aslam, Department of Oncology, King Faisal Specialist Hospital and Research Centre, Po Box 40047, Jeddah, 21499 Kingdom of Saudi Arabia
	

	
		Journal Annals of HematologyOnline IS...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5639126</comments>
            <pubDate>Tue, 24 Jan 2012 12:25:50 +0100</pubDate>
            <guid isPermaLink="false">5639126</guid>        </item>
        <item>
            <title>Inhibition of p38 MAPK activity promotes ex vivo expansion of human cord blood hematopoietic stem cells</title>
            <link>http://www.medworm.com/index.php?rid=5620904&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl7133220l34l0155%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Ex vivo expansion of hematopoietic stem cells (HSCs) depends on HSC self-renewing proliferation and functional maintenance,
 which can be negatively affected by HSC differentiation, apoptosis, and senescence. Therefore, inhibition of HSC senescence
 may promote HSC expansion. To test this hypothesis, we examined the effect of inhibition of p38 mitogen-activated protein
 kinase (p38) on the expansion of human umbilical cord blood (hUCB) CD133+ cells because activation of p38 has been implicated in the induction of HSC senescence under various physiological and pathological
 conditions. Our results showed that ex vivo expansion of hUCB CD133+ cells activated p38, which was abrogated by the p38 specific inhibitor SB203580 (SB). Inhibition of p38 activity with SB
 promoted ...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5620904</comments>
            <pubDate>Thu, 19 Jan 2012 08:04:29 +0100</pubDate>
            <guid isPermaLink="false">5620904</guid>        </item>
        <item>
            <title>Prothrombin complex concentrate (Octaplex®) for postsurgical bleeding control in a Stauffer’s syndrome</title>
            <link>http://www.medworm.com/index.php?rid=5620905&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk8k4200310jp73l3%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorPages 1-2DOI 10.1007/s00277-011-1396-8Authors
		Ana B. Fernández, Anaesthesiology and Intensive Care Department, Nuestra Sra de Candelaria University Hospital, Tenerife, Canary Islands, SpainAzahara Sancho de Ávila, Anaesthesiology and Intensive Care Department, Nuestra Sra de Candelaria University Hospital, Tenerife, Canary Islands, Spain
	

	
		Journal Annals of HematologyOnline ISSN 1432-0584Print ISSN 0939-5555 (Source: Annals of Hematology)</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5620905</comments>
            <pubDate>Thu, 19 Jan 2012 08:04:28 +0100</pubDate>
            <guid isPermaLink="false">5620905</guid>        </item>
        <item>
            <title>Adult onset of primary hemophagocytic syndrome in subjects carrying PRF1 mutations</title>
            <link>http://www.medworm.com/index.php?rid=5620906&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F1t35586381345764%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorPages 1-2DOI 10.1007/s00277-012-1409-2Authors
		Yini Wang, Department of Hematology, Beijing Friendship Hospital, Capital Medical University, Beijing, ChinaZhao Wang, Department of Hematology, Beijing Friendship Hospital, Capital Medical University, Beijing, ChinaHua Chen, Department of Hematology, Beijing Friendship Hospital, Capital Medical University, Beijing, ChinaXiaolin Wang, Department of Hematology, Beijing Friendship Hospital, Capital Medical University, Beijing, China
	

	
		Journal Annals of HematologyOnline ISSN 1432-0584Print ISSN 0939-5555 (Source: Annals of Hematology)</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5620906</comments>
            <pubDate>Tue, 17 Jan 2012 07:12:46 +0100</pubDate>
            <guid isPermaLink="false">5620906</guid>        </item>
        <item>
            <title>Toxoplasmosis after allogeneic stem cell transplantation—a single centre experience</title>
            <link>http://www.medworm.com/index.php?rid=5620907&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg618414n7v2310n2%2F</link>
            <description>In conclusion, we suggest a rigorous real-time PCR monitoring for high-risk patients or patients with signs of infections
 suspicious for toxoplasmosis, even though low-copy results are presently difficult to interpret. Our reported cases might
 also encourage the use of trimethoprim–sufmethoxazole instead of pentamidine for PcP prophylaxis in those patients.
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-9DOI 10.1007/s00277-012-1406-5Authors
		Christoph Busemann, Department of Internal Medicine C (Haematology and Oncology, Marrow Transplantation), Ernst-Moritz-Arndt-University Greifswald, Ferdinand-Sauerbruch-Str, 17475 Greifswald, GermanySilvia Ribback, Institute for Pathology, Ernst-Moritz-Arndt-University Greifswald, Ferdinand-Sauerbruch-Str, 17475 Greifswald, Germ...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5620907</comments>
            <pubDate>Tue, 17 Jan 2012 07:12:45 +0100</pubDate>
            <guid isPermaLink="false">5620907</guid>        </item>
        <item>
            <title>Association of CD20 levels with clinicopathological parameters and its prognostic significance for patients with DLBCL</title>
            <link>http://www.medworm.com/index.php?rid=5620908&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp31871j13p2u8585%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Diffuse large B-cell lymphomas (DLBCL) express CD20. CD20 expression is described as negative, weak, or normal as determined
 by flow cytometry (FCM) and is an important target for the treatment of DLBCL. However, the impact of CD20 levels at onset
 of the disease on patient prognosis has not been fully elucidated. We analyzed 174 DLBCL cases newly diagnosed between January
 1998 and April 2010. The relationship of the association between CD20 levels and patients’ backgrounds and prognoses was analyzed
 using the Kaplan–Meier method and Cox proportional hazard regression. Of the 174 patients, three cases (1.7%) were defined
 as CD20 negative based on immunohistochemistry (IHC). Although the other 171 cases were positive by IHC, eight cases (4.7%)
 were defined as ne...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5620908</comments>
            <pubDate>Tue, 17 Jan 2012 07:12:44 +0100</pubDate>
            <guid isPermaLink="false">5620908</guid>        </item>
        <item>
            <title>Ferroportin (SLC40A1) Q248H mutation is associated with lower circulating serum hepcidin levels in Rwandese HIV-positive women</title>
            <link>http://www.medworm.com/index.php?rid=5620909&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F7702273840jr1k42%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The Q248H mutation in the gene SLC40A1 which encodes for the cellular iron exporter ferroportin is relatively common in Africa.
 This mutation has been associated with resistance to hepcidin and therefore we hypothesized that iron-related parameters and
 the prevalence of opportunistic infections in HIV might be influenced by the Q248H mutation. We conducted a cross-sectional
 study among 200 HIV-positive women in the Butare University Teaching Hospital in Rwanda. Polymerase chain reaction (PCR) and
 restriction enzyme digestion were used to identify the Q248H mutation. Physical examination was carried out and WHO HIV disease
 stage classification, complete blood count, CD4 count, indirect measures of iron status, serum hepcidin, and C-reactive protein
 concentrations w...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5620909</comments>
            <pubDate>Tue, 17 Jan 2012 07:12:40 +0100</pubDate>
            <guid isPermaLink="false">5620909</guid>        </item>
        <item>
            <title>Allogeneic hematopoietic stem cell transplantation in patients with diffuse large B cell lymphoma relapsed after autologous stem cell transplantation: A GITMO study</title>
            <link>http://www.medworm.com/index.php?rid=5598823&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fum4u206144437v3t%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Patients who relapse after an autologous hematopoietic stem cell transplantation (SCT) have a very poor prognosis. We have
 retrospectively analyzed diffuse large B cell lymphoma patients who underwent an allo-SCT after an auto-SCT relapse reported
 in the Gruppo Italiano Trapianto di Midollo Osseo (GITMO) database. From 1995 to 2008, 3449 autologous transplants were reported
 in the GITMO database. Eight hundred eighty-four patients relapsed or progressed after transplant; 165 patients, 19% of the
 relapsed patients, were treated with allo-transplant. The stem cell donor was related to the patient in 108 cases. A reduced
 intensity conditioning regimen was used in 116. After allo-SCT, 72 patients (43%) obtained a complete response and 9 obtained
 a partial response wit...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5598823</comments>
            <pubDate>Fri, 13 Jan 2012 16:58:16 +0100</pubDate>
            <guid isPermaLink="false">5598823</guid>        </item>
        <item>
            <title>Posterior reversible encephalopathy syndrome (PRES) during induction chemotherapy for acute myeloblastic leukemia (AML)</title>
            <link>http://www.medworm.com/index.php?rid=5598825&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp720724037768664%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorPages 1-2DOI 10.1007/s00277-011-1398-6Authors
		Giorgia Battipaglia, Department of Biochemistry and Medical Biotechnology, Federico II University, via Pansini 5, 80131 Naples, ItalySimona Avilia, Department of Biochemistry and Medical Biotechnology, Federico II University, via Pansini 5, 80131 Naples, ItalyEmanuela Morelli, Department of Biochemistry and Medical Biotechnology, Federico II University, via Pansini 5, 80131 Naples, ItalyFerdinando Caranci, Diagnostic Imaging and Radiotherapy, Federico II University, Naples, ItalyFabiana Perna, Department of Biochemistry and Medical Biotechnology, Federico II University, via Pansini 5, 80131 Naples, ItalyAndrea Camera, Department of Biochemistry and Medical Biotechnology, Federico II U...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5598825</comments>
            <pubDate>Thu, 12 Jan 2012 06:42:55 +0100</pubDate>
            <guid isPermaLink="false">5598825</guid>        </item>
        <item>
            <title>Cyclophosphamide-containing regimen (TCD) is superior to melphalan-containing regimen (MPT) in elderly multiple myeloma patients with renal impairment</title>
            <link>http://www.medworm.com/index.php?rid=5598824&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fy88135488425630m%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Renal impairment (RI) is a frequent complication with higher incidence of infections and an important prognostic factor for
 survival. Melphalan clearance is renal function dependent whereas cyclophosphamide is renal function independent. We investigated
 which combination regimen should be selected between melphalan-combining regimen (MPT) or cyclophosphamide-combining regimen
 (TCD) in elderly multiple myeloma (MM) patients with RI. Between 2005 and 2009, 157 newly diagnosed MM patients with RI were
 included comparing MPT with TCD therapy as initial treatment. Seventy-four patients were given MPT regimen, and 83 patients
 were given TCD regimen. Baseline characteristics were similar between the MPT and TCD groups. Analysis of different cutoff
 levels between 25% and ...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5598824</comments>
            <pubDate>Thu, 12 Jan 2012 06:42:55 +0100</pubDate>
            <guid isPermaLink="false">5598824</guid>        </item>
        <item>
            <title>Langerhans/dendritic cell sarcoma arising from hairy cell leukemia: a rare phenomenon</title>
            <link>http://www.medworm.com/index.php?rid=5583444&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fq3254q41365rp33n%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorPages 1-3DOI 10.1007/s00277-011-1399-5Authors
		Alaa Muslimani, Department of Hematology and Oncology, Oakland University William Beaumont School of Medicine, William Beaumont Hospital, 3577 W 13 Mile Rd, Suite 202, Royal Oak, MI 48073, USAMohammad Muhsin Chisti, Department of Hematology and Oncology, Oakland University William Beaumont School of Medicine, William Beaumont Hospital, 3577 W 13 Mile Rd, Suite 202, Royal Oak, MI 48073, USAAnn Marie Blenc, Department of Pathology, Oakland University William Beaumont School of Medicine, William Beaumont Hospital, 3601 W 13 Mile Rd, Royal Oak, MI 48073, USAIqbal Boxwala, Department of Hematology and Oncology, Oakland University William Beaumont School of Medicine, William Beaumont Hospit...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5583444</comments>
            <pubDate>Wed, 11 Jan 2012 06:57:54 +0100</pubDate>
            <guid isPermaLink="false">5583444</guid>        </item>
        <item>
            <title>Non-atopic IgE and eosinophil cationic protein after allogeneic hematopoietic stem cell transplantation in children</title>
            <link>http://www.medworm.com/index.php?rid=5583445&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fgj1t713501h1h75t%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Allogeneic hematopoietic stem cell transplantation (HSCT) in childhood is associated with severe pulmonary complications,
 but the pathophysiologic mechanisms remain unclear. Our aim was to evaluate the association of total and specific IgE, eosinophil
 cationic protein (ECP) and eosinophilia in HSCT recipients with pulmonary complications. We prospectively measured total and
 specific serum IgE, eosinophils, and ECP before and 28, 100, and 180&amp;nbsp;days after HSCT. We included 30 children (age 2–17&amp;nbsp;years)
 undergoing HSCT. Nine patients had a history of previous atopy without being associated with pulmonary complications after
 HSCT until day +360. Specific IgE levels showed a decline after HSCT, associated with the absence of allergy symptoms, suggesting
 a red...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5583445</comments>
            <pubDate>Wed, 11 Jan 2012 06:57:53 +0100</pubDate>
            <guid isPermaLink="false">5583445</guid>        </item>
        <item>
            <title>Imatinib trough plasma levels do not correlate with the response to therapy in patients with chronic myeloid leukemia in routine clinical setting</title>
            <link>http://www.medworm.com/index.php?rid=5583446&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu626703g562881n1%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Association of trough imatinib plasma levels (IPL) with cytogenetic or molecular response to treatment in patients with chronic
 myeloid leukemia (CML) was repeatedly reported. We analyzed their value in the routine clinical setting in 131 patients with
 chronic phase CML in whom imatinib was applied as first- or second-line treatment. A total of 1,118 measurements were obtained
 by ultra-performance liquid chromatography–tandem mass spectrometry assay in patients treated with daily dose of imatinib
 ranging from 100 to 800&amp;nbsp;mg. Samples were obtained from 1 to 96&amp;nbsp;h after drug ingestion. High inter (36%) and intraindividual
 variability (9–33%) of IPL was observed. For analysis of correlation of IPL with treatment response, two sets of samples were
 selected...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5583446</comments>
            <pubDate>Tue, 10 Jan 2012 06:46:46 +0100</pubDate>
            <guid isPermaLink="false">5583446</guid>        </item>
        <item>
            <title>The proteasome inhibitor bortezomib targets cell cycle and apoptosis and acts synergistically in a sequence-dependent way with chemotherapeutic agents in mantle cell lymphoma</title>
            <link>http://www.medworm.com/index.php?rid=5583447&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb22wr5x144311268%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Single-agent bortezomib, a potent, selective, and reversible inhibitor of the 26S proteasome, has demonstrated clinical efficacy
 in relapsed and refractory mantle cell lymphoma (MCL). Objective response is achieved in up to 45% of the MCL patients; however,
 complete remission rates are low and duration of response proved to be relatively short. These limitations may be overcome
 by combining proteasome inhibition with conventional chemotherapy. Rational combination treatment and schedules require profound
 knowledge of underlying molecular mechanisms. Here we show that single-agent bortezomib treatment of MCL cell lines leads
 to G2/M arrest and induction of apoptosis accompanied by downregulation of EIF4E and CCND1 mRNA but upregulation of p15(INK4B)
 and p21 mRNA. W...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5583447</comments>
            <pubDate>Tue, 10 Jan 2012 06:46:45 +0100</pubDate>
            <guid isPermaLink="false">5583447</guid>        </item>
        <item>
            <title>Concurrent search for unrelated cord and volunteer donor in high-risk acute lymphoblastic leukemia</title>
            <link>http://www.medworm.com/index.php?rid=5561304&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ff261204x04p37411%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;To assess the effectiveness of the search for an unrelated donor on the outcome of patients with high-risk acute lymphoblastic
 leukemia, we analyzed prospectively 136 patients who underwent a search for cord blood (CB) and an unrelated volunteer donor
 (UD) at the same time. The probability of finding a donor was 58.2%, 70.3%, and 75.7% at 3, 6, and 12&amp;nbsp;months, respectively.
 The median time to find a donor was 1.8&amp;nbsp;months for CB and 3.5&amp;nbsp;months for UD. Of the 99 patients with a donor, 38.4% failed
 to undergo the transplant because of a relapse observed at a median of 4&amp;nbsp;months from the start of the search. In univariate
 analysis, absence of relapse during the search (p &amp;lt; 0.0001) and transplant (p = 0.004) showed a positive impact on long-t...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5561304</comments>
            <pubDate>Mon, 02 Jan 2012 06:58:18 +0100</pubDate>
            <guid isPermaLink="false">5561304</guid>        </item>
        <item>
            <title>Chronic lymphocytic leukemia and prolymphocytic leukemia with MYC translocations: a subgroup with an aggressive disease course</title>
            <link>http://www.medworm.com/index.php?rid=5561305&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F5427101457431826%2F</link>
            <description>In conclusion, CLL/PLL with MYC translocations is a rare entity, which seems to be associated with adverse prognostic features and unfavorable outcome.
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-11DOI 10.1007/s00277-011-1393-yAuthors
		Natalie Put, Center for Human Genetics, Catholic University of Leuven, Herestraat 49, 3000 Leuven, BelgiumKatrien Van Roosbroeck, Center for Human Genetics, Catholic University of Leuven, Herestraat 49, 3000 Leuven, BelgiumPeter Konings, Department of Electrical Engineering/IBBT-K.U. Leuven Future Health Department, Catholic University of Leuven, Leuven, BelgiumPeter Meeus, Center for Human Genetics, Catholic University of Leuven, Herestraat 49, 3000 Leuven, BelgiumCaroline Brusselmans, Department of Clinical Biology, University Hospit...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5561305</comments>
            <pubDate>Thu, 29 Dec 2011 06:42:41 +0100</pubDate>
            <guid isPermaLink="false">5561305</guid>        </item>
        <item>
            <title>The role of human leukocyte antigens as predisposing and/or protective factors in patients with idiopathic thrombotic thrombocytopenic purpura</title>
            <link>http://www.medworm.com/index.php?rid=5553050&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fd7n3q538p577081u%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Fifty-four adult German patients suffering from idiopathic thrombotic thrombocytopenic purpura (TTP) have been examined for
 HLA class II. All patients presented autoantibodies against ADAMTS13 and ADAMTS13 activity levels &amp;lt;5%. Blood samples have
 been analyzed for HLA-DRB1 and DQB1 alleles using sequence-specific primer PCR and sequence-specific oligonucleotide PCR.
 Reference data of German bone marrow and blood donors were obtained from www.allelefrequencies.net. The results were evaluated employing two-sided binomial tests, and p values were corrected using the Benjamini–Hochberg procedure. A significant accumulation for DQB1*02:02 (p &amp;lt; 0.001) and DRB1*11 (p = 0.003) was found within the patient group. Twenty percent (DQB1*02:02) or 48.1% (DRB1*11) o...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5553050</comments>
            <pubDate>Tue, 27 Dec 2011 16:51:21 +0100</pubDate>
            <guid isPermaLink="false">5553050</guid>        </item>
        <item>
            <title>Treatment of B cell lymphoma with chemotherapy plus rituximab: a survival benefit can be demonstrated in the routine data of a regional cancer registry</title>
            <link>http://www.medworm.com/index.php?rid=5553051&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fllm818u7473pkx6l%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Combination of standard chemotherapy with rituximab led to improved disease control in patients with B cell lymphoma in clinical
 trials. We wanted to know if a similar benefit could be demonstrated in the routine data of a regional population-based cancer
 registry. We searched the registry of the Regensburg Tumor Center for B cell non-Hodgkin lymphomas diagnosed between 1998
 and 2006 and compared overall survival of patients receiving any first-line chemotherapy with or without rituximab. Comparing
 registry data to death certificates, an 86% coverage within the registry was estimated. In the aggressive lymphoma group,
 133 patients received rituximab-containing chemotherapy resulting in a 5-year survival of 69.6%, whereas 205 patients received
 chemotherapy alone wi...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5553051</comments>
            <pubDate>Tue, 27 Dec 2011 06:33:55 +0100</pubDate>
            <guid isPermaLink="false">5553051</guid>        </item>
        <item>
            <title>First report of incidence of adult myelodysplastic syndrome in China</title>
            <link>http://www.medworm.com/index.php?rid=5545195&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F46144072v0u43942%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorPages 1-2DOI 10.1007/s00277-011-1389-7Authors
		Wei Wang, Hematology Department, Huashan Hospital of Fudan University, Wulumuqi Central Road No 12, Shanghai, 200040 ChinaHong Wang, Hematology Department, Huashan Hospital of Fudan University, Wulumuqi Central Road No 12, Shanghai, 200040 ChinaXiao-Qin Wang, Hematology Department, Huashan Hospital of Fudan University, Wulumuqi Central Road No 12, Shanghai, 200040 ChinaGuo-Wei Lin, Hematology Department, Huashan Hospital of Fudan University, Wulumuqi Central Road No 12, Shanghai, 200040 China
	

	
		Journal Annals of HematologyOnline ISSN 1432-0584Print ISSN 0939-5555 (Source: Annals of Hematology)</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5545195</comments>
            <pubDate>Thu, 22 Dec 2011 12:51:03 +0100</pubDate>
            <guid isPermaLink="false">5545195</guid>        </item>
        <item>
            <title>Extreme eosinophilia in a setting of metastatic leiomyosarcoma: An unusual case report</title>
            <link>http://www.medworm.com/index.php?rid=5545196&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ftq78781675282384%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorPages 1-2DOI 10.1007/s00277-011-1391-0Authors
		Arwa Z. Al-Riyami, Division of Hematological Pathology, Department of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, BC, CanadaPeter W. K. Tsang, Division of Hematology, University of British Columbia, Vancouver, BC, CanadaMonika Hudoba, Department of Pathology and Laboratory Medicine, Vancouver General Hospital and University of British Columbia, Vancouver, BC, Canada
	

	
		Journal Annals of HematologyOnline ISSN 1432-0584Print ISSN 0939-5555 (Source: Annals of Hematology)</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5545196</comments>
            <pubDate>Thu, 22 Dec 2011 12:51:02 +0100</pubDate>
            <guid isPermaLink="false">5545196</guid>        </item>
        <item>
            <title>Plasmacytic differentiation in MALT lymphomas following treatment with rituximab</title>
            <link>http://www.medworm.com/index.php?rid=5545197&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ft58462482144t263%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Mucosa-associated lymphoid tissue (MALT) lymphomas are B cell neoplasms which commonly affect the gastrointestinal (GI) tract.
 Gastrointestinal MALT lymphomas rarely show plasmacytic differentiation (PCD), and limited data on the potential influence
 of the anti-CD20 antibody rituximab (R) on PCD exist in the current literature. We have retrospectively analyzed patients
 with GI MALT lymphomas treated with R-containing regimens because restaging is routinely performed by repeated biopsies with
 pathohistological response assessment. Twenty-one patients with GI MALT lymphoma were identified to have undergone R-containing
 therapy. In 19 patients, the lymphoma originated in the stomach, while the colon was the primarily affected organ in two cases.
 Four patients receive...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5545197</comments>
            <pubDate>Wed, 21 Dec 2011 19:46:42 +0100</pubDate>
            <guid isPermaLink="false">5545197</guid>        </item>
        <item>
            <title>High prevalence of hepatitis B virus infection in HIV-negative Castleman's disease</title>
            <link>http://www.medworm.com/index.php?rid=5545198&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F23wp023633467108%2F</link>
            <description>In conclusion, our findings suggest an association between HBV infection and development of CD. CD patients with
 HBV infection have their own distinguished features.
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-5DOI 10.1007/s00277-011-1388-8Authors
		Xiang-Gui Yuan, The Second Affiliated Hospital (Binjiang Branch), School of Medicine, Zhejiang University; Department of Internal Medicine, Hangzhou Binjiang Hospital, Hangzhou, China 310009Fei-Fei Chen, Department of Hematology, the First Affiliated Hospital, School of Medicine, Zhejiang University, #79 Qingchun Road, Hangzhou, China 310003Yi-Miao Zhu, The Second Affiliated Hospital (Binjiang Branch), School of Medicine, Zhejiang University; Department of Internal Medicine, Hangzhou Binjiang Hospital, Hangzhou, China 310...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5545198</comments>
            <pubDate>Wed, 21 Dec 2011 19:46:41 +0100</pubDate>
            <guid isPermaLink="false">5545198</guid>        </item>
        <item>
            <title>A novel ELISA for diagnosis of Glanzmann’s thrombasthenia and the heterozygote carriers</title>
            <link>http://www.medworm.com/index.php?rid=5538777&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Flt3240k353345797%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A sensitive and specific sandwich ELISA was developed for the diagnosis of Glanzmann’s thrombasthenia (GT) and the heterozygote
 carriers of the disease using whole blood platelets. The assay used anti-CD36 antibody to capture platelets from platelet-rich
 plasma which was subsequently treated with a bioengineered disintegrin/alkaline phosphatase hybrid protein specific for GP
 IIb/IIIa. The test allows large number of samples to be typed and can also be used on stored samples. The assay correctly
 diagnosed 40 normal healthy individuals, 10 GT cases, 10 heterozygotes, 3 Bernard–Soulier syndrome cases and 2 type 3 GT cases.
 ELISA plates were stable at room temperature up to 3&amp;nbsp;weeks without any loss of activity. This novel and simple test can be
 widely used fo...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5538777</comments>
            <pubDate>Tue, 20 Dec 2011 06:43:20 +0100</pubDate>
            <guid isPermaLink="false">5538777</guid>        </item>
        <item>
            <title>Serum soluble interleukin-2 receptor (sIL-2R) level is associated with the outcome of patients with diffuse large B cell lymphoma treated with R-CHOP regimens</title>
            <link>http://www.medworm.com/index.php?rid=5538778&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F480t365827tpu1r6%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Serum concentration of soluble interleukin-2 receptor (sIL-2R) predicts the clinical outcome of patients with aggressive non-Hodgkin's
 lymphoma treated with the cyclophosphamide, doxorubicin, vincristine, and prednisolone (CHOP) regimen without rituximab. In
 the present study, we aim to re-assess the prognostic significance of serum sIL-2R for diffuse large B cell lymphoma (DLBCL)
 patients treated with CHOP plus rituximab and to assess sIL-2R with subtype of DLBCL, such as GCB type and non-GCB type. Two
 hundred and thirty-three patients with DLBCL were enrolled between December 2002 and March 2008. To evaluate serum levels
 of sIL-2R, venous blood samples were drawn from patients immediately before initiation of treatment. Serum sIL-2R was determined
 by sandwich en...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5538778</comments>
            <pubDate>Tue, 20 Dec 2011 06:43:19 +0100</pubDate>
            <guid isPermaLink="false">5538778</guid>        </item>
        <item>
            <title>Extracorporeal light chain elimination: high cut-off (HCO) hemodialysis parallel to chemotherapy allows for a high proportion of renal recovery in multiple myeloma patients with dialysis-dependent acute kidney injury</title>
            <link>http://www.medworm.com/index.php?rid=5516056&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Flu70003761741366%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Acute kidney injury (AKI) is frequent in multiple myeloma (MM) patients and strongly affects prognosis, with particularly
 poor outcomes in patients requiring hemodialysis. Introduction of the novel therapeutic agents to MM therapy has improved
 myeloma response and renal outcome. This case series reviews the efficacy of combined systemic and extracorporeal therapy
 to further optimize time to light chain (serum-free light chain (sFLC)) reduction and renal recovery in MM patients with dialysis-dependent
 AKI (n = 19). High cut-off (HCO) hemodialysis for extracorporeal sFLC removal was initiated in parallel to chemotherapy. Combined
 therapy resulted in early sFLC response after a median of 13 (range 4–48) days and 6 (3–22) HCO hemodialysis sessions. Time
 to sFL...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5516056</comments>
            <pubDate>Wed, 14 Dec 2011 16:31:04 +0100</pubDate>
            <guid isPermaLink="false">5516056</guid>        </item>
        <item>
            <title>A useful relationship between the presence of extramedullary erythropoeisis and the level of the soluble form of the transferrin receptor in a large cohort of adult patients with thalassemia intermedia: a prospective study</title>
            <link>http://www.medworm.com/index.php?rid=5516057&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl007t21154232214%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;In thalassemia intermedia (TI), the increase in bone marrow hemopoietic activity frequently leads to extramedullary erythropoeisis
 (EMH), but its relationship with the soluble form of transferrin receptor (sTfR) which fully reflects the marrow erythropoietic
 activity, has not yet been explored. From January 2007 to December 2010, all TI patients attending at our center were prospectively
 enrolled to undergo sTfR assay and MRI or CT (if claustrophobic) scan evaluation for the presence of paraspinal EMH. A total
 of 59 patients with TI were studied; EMH involved 23 (39%) patients; overall, the concentration of sTfR varied from 2.6 to
 20.6 (mean = 8.7) mg/L, but in splenectomized group and in unsplenectomized group, it varied from 4.2 to 17.8 (mean ± SD = ...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5516057</comments>
            <pubDate>Wed, 14 Dec 2011 06:57:33 +0100</pubDate>
            <guid isPermaLink="false">5516057</guid>        </item>
        <item>
            <title>No association between Agent Orange exposure and monoclonal gammopathies</title>
            <link>http://www.medworm.com/index.php?rid=5506144&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F77701032274m2317%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorPages 1-2DOI 10.1007/s00277-011-1382-1Authors
		Jignesh G. Parikh, Department of Pathology, University of Tennessee Health Science Center, Memphis, TN, USAEugene Pearlman, Department of Pathology, University of Tennessee Health Science Center, Memphis, TN, USA
	

	
		Journal Annals of HematologyOnline ISSN 1432-0584Print ISSN 0939-5555 (Source: Annals of Hematology)</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5506144</comments>
            <pubDate>Mon, 12 Dec 2011 06:33:04 +0100</pubDate>
            <guid isPermaLink="false">5506144</guid>        </item>
        <item>
            <title>Rituximab in combination with CHOP chemotherapy for the treatment of diffuse large B cell lymphoma in China: a 10-year retrospective follow-up analysis of 437 cases from Shanghai Lymphoma Research Group</title>
            <link>http://www.medworm.com/index.php?rid=5495498&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv447rpl124k04r14%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The purpose of the study is to evaluate the 10&amp;nbsp;years follow-up of the efficacy in Chinese patients receiving cyclophosphamide,
 doxorubicin/epirubicin, vincristine, and prednisone (CHOP) or rituximab plus CHOP (R-CHOP) regimen as the initial treatment
 for diffuse large B cell lymphoma (DLBCL). We have retrospectively analyzed 437 patients with DLBCL who were newly diagnosed
 and received CHOP or R-CHOP regimen in six university hospitals and closely followed up after the completion of treatment.
 For all patients, there were significant differences between R-CHOP and CHOP for overall survival (OS) (median follow-up 86&amp;nbsp;months,
 84.1% vs 70.2%, p = 0.018) and progression-free survival (PFS) (81.5% vs 66.7%, p = 0.015), while elder patients (&amp;gt;60&amp;nbsp;...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5495498</comments>
            <pubDate>Thu, 08 Dec 2011 07:21:23 +0100</pubDate>
            <guid isPermaLink="false">5495498</guid>        </item>
        <item>
            <title>Postpartum anemia II: prevention and treatment</title>
            <link>http://www.medworm.com/index.php?rid=5495499&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fcxu65432713747vj%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;This review focuses on the prevention and treatment of anemia in women who have just given childbirth (postpartum anemia).
 The problem of anemia both prepartum and postpartum is far more prevalent in developing countries than in the Western societies.
 The conditions for mother and child in the postpartum, nursing, and lactation period should be as favorable as possible. Many
 young mothers have a troublesome life due to iron deficiency and iron deficiency anemia (IDA) causing a plethora of symptoms
 including fatigue, physical disability, cognitive problems, and psychiatric disorders. Routine screening for postpartum anemia
 should be considered as part of the national maternal health programs. Major causes of postpartum anemia are prepartum iron
 deficiency and IDA i...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5495499</comments>
            <pubDate>Thu, 08 Dec 2011 07:21:21 +0100</pubDate>
            <guid isPermaLink="false">5495499</guid>        </item>
        <item>
            <title>Clinical features of adult patients with secondary hemophagocytic lymphohistiocytosis from causes other than lymphoma: an analysis of treatment outcome and prognostic factors</title>
            <link>http://www.medworm.com/index.php?rid=5487920&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm8817g44jr855585%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Although hemophagocytic syndrome (HS) featuring secondary hemophagocytic lymphohistiocytosis (HLH) has a grave prognosis,
 little is known about the natural course of the disease. Patients who showed the clinical features of HLH as well as tissue-proven
 hemophagocytosis when seen at Asan Medical Center between 1999 and 2010 were included in this analysis. Patients with proven
 lymphoma were excluded. The median age of our 23 study patients was 49&amp;nbsp;years. Epstein–Barr virus was suspected to have caused
 HS in 16 (70%) patients and hepatitis A virus in one patient. Twenty-two patients were treated, 13 according to the HLH protocol
 and nine using immunosuppressive agents such as corticosteroid and/or cyclosporine. Five patients undertook allogeneic hematopoietic
 c...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5487920</comments>
            <pubDate>Wed, 07 Dec 2011 10:51:12 +0100</pubDate>
            <guid isPermaLink="false">5487920</guid>        </item>
        <item>
            <title>Lymphoma with specific affinity to endocrine organs</title>
            <link>http://www.medworm.com/index.php?rid=5487922&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fr30x5l42q14u6667%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorPages 1-2DOI 10.1007/s00277-011-1372-3Authors
		Ken Morita, Department of Hematology &amp; Oncology, Graduate School of Medicine, The University of Tokyo, Tokyo, JapanFumihiko Nakamura, Department of Hematology &amp; Oncology, Graduate School of Medicine, The University of Tokyo, Tokyo, JapanYasuhito Nannya, Department of Hematology &amp; Oncology, Graduate School of Medicine, The University of Tokyo, Tokyo, JapanYasuhiko Kamikubo, Department of Hematology &amp; Oncology, Graduate School of Medicine, The University of Tokyo, Tokyo, JapanMotoshi Ichikawa, Department of Hematology &amp; Oncology, Graduate School of Medicine, The University of Tokyo, Tokyo, JapanMineo Kurokawa, Department of Hematology &amp; Oncology, Graduate School of Medicine, The Univers...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5487922</comments>
            <pubDate>Tue, 06 Dec 2011 17:03:02 +0100</pubDate>
            <guid isPermaLink="false">5487922</guid>        </item>
        <item>
            <title>Prognostic value of red blood cell parameters and ferritin in predicting deferral due to low hemoglobin in whole blood donors</title>
            <link>http://www.medworm.com/index.php?rid=5487921&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F29t1g52683518115%2F</link>
            <description>In conclusion, pre-donation
 hemoglobin is a useful marker identifying donors at risk of developing low hemoglobin levels. Diagnostic and therapeutic interventions
 should be aimed at donors presenting with hemoglobin levels near the threshold of donor deferral.
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-6DOI 10.1007/s00277-011-1371-4Authors
		Martin Stern, Division of Hematology, Department of Internal Medicine, University Hospital Basel, Basel, SwitzerlandAlix O’Meara, Division of Hematology, Department of Internal Medicine, University Hospital Basel, Basel, SwitzerlandLaura Infanti, Blood Transfusion Center, Swiss Red Cross, Basel, Hebelstrasse 10, 4031 Basel, SwitzerlandJoerg-Peter Sigle, Blood Transfusion Center, Swiss Red Cross, Basel, Hebelstrasse 10, 4031 B...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5487921</comments>
            <pubDate>Tue, 06 Dec 2011 17:03:02 +0100</pubDate>
            <guid isPermaLink="false">5487921</guid>        </item>
        <item>
            <title>Anti-thrombin-III reduction and posterior reversible encephalopathy syndrome (PRES) in acute lymphoblastic leukaemia (ALL). New insight into PRES pathophysiology</title>
            <link>http://www.medworm.com/index.php?rid=5477405&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F264t21332u634412%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorPages 1-3DOI 10.1007/s00277-011-1376-zAuthors
		Andrea Piccin, Department of Haematology and Bone Marrow Transplant Unit, San Maurizio Regional Hospital, Bolzano, South Tyrol, ItalyRoberto Currò Dossi, Stroke Unit, Department of Internal Medicine, San Maurizio Regional Hospital, Bolzano, South Tyrol, ItalyVincenzo Cassibba, Department of Haematology and Bone Marrow Transplant Unit, San Maurizio Regional Hospital, Bolzano, South Tyrol, ItalySigmund Stupnner, Department of Radiology, San Maurizio Regional Hospital, Bolzano, South Tyrol, ItalyGiampietro Bonatti, Department of Radiology, San Maurizio Regional Hospital, Bolzano, South Tyrol, ItalySergio Cortelazzo, Department of Haematology and Bone Marrow Transplant Unit, San Maurizio...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5477405</comments>
            <pubDate>Fri, 02 Dec 2011 06:48:14 +0100</pubDate>
            <guid isPermaLink="false">5477405</guid>        </item>
        <item>
            <title>Aberrant expression of myeloid and B cell markers in an aggressive multiple-site myeloid sarcoma</title>
            <link>http://www.medworm.com/index.php?rid=5477406&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fhjt122g727w12u87%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorPages 1-3DOI 10.1007/s00277-011-1378-xAuthors
		Georgia D. Kaiafa, Department of Haematology, First Propedeutic Department of Internal Medicine, Aristotle University of Thessaloniki, AHEPA General Hospital, 1 S. Kiriakidi St, 546 36 Thessaloniki, GreeceVasilios Perifanis, Department of Haematology, First Propedeutic Department of Internal Medicine, Aristotle University of Thessaloniki, AHEPA General Hospital, 1 S. Kiriakidi St, 546 36 Thessaloniki, GreeceMichael D. Diamantidis, Department of Haematology, First Propedeutic Department of Internal Medicine, Aristotle University of Thessaloniki, AHEPA General Hospital, 1 S. Kiriakidi St, 546 36 Thessaloniki, GreeceOlga Giouleme, Department of Gastroenterology, First Propedeutic Departm...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5477406</comments>
            <pubDate>Fri, 02 Dec 2011 06:48:13 +0100</pubDate>
            <guid isPermaLink="false">5477406</guid>        </item>
        <item>
            <title>Neurolymphomatosis: role of positron emission tomography in diagnosis</title>
            <link>http://www.medworm.com/index.php?rid=5477407&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fr11506259q813713%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorPages 1-2DOI 10.1007/s00277-011-1379-9Authors
		Carol Cheung, Department of Medicine, Queen Mary Hospital, Professorial Block, Pokfulam Road, Hong Kong, ChinaDavid Lopes, Department of Haematology, Hospital Conde S. Januario, Macau, ChinaKwan-Ngai Hung, Department of Surgery, Queen Mary Hospital, Hong Kong, ChinaTao Chan, Department of Diagnostic Radiology, Queen Mary Hospital, Hong Kong, ChinaKwok-Wah Chan, Department of Pathology, Queen Mary Hospital, Hong Kong, ChinaYok-Lam Kwong, Department of Medicine, Queen Mary Hospital, Professorial Block, Pokfulam Road, Hong Kong, China
	

	
		Journal Annals of HematologyOnline ISSN 1432-0584Print ISSN 0939-5555 (Source: Annals of Hematology)</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5477407</comments>
            <pubDate>Thu, 01 Dec 2011 06:59:21 +0100</pubDate>
            <guid isPermaLink="false">5477407</guid>        </item>
        <item>
            <title>A prospective survey of febrile events in hematological malignancies</title>
            <link>http://www.medworm.com/index.php?rid=5458897&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fc3371026125w78t2%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The Hema e-Chart prospectively collected data on febrile events (FEs) in hematological malignancy patients (HMs). The aim
 of the study was to assess the number, causes and outcome of HM-related FEs. Data were collected in a computerized registry
 that systematically approached the study and the evolution of FEs developing in a cohort of adult HMs who were admitted to
 19 hematology departments in Italy from March 2007 to December 2008. A total of 869 FEs in 3,197 patients with newly diagnosed
 HMs were recorded. Fever of unidentified origin (FUO) was observed in 386 cases (44.4%). The other causes of FE were identified
 as noninfectious in 48 cases (5.5%) and infectious in 435 cases (50.1%). Bacteria were the most common cause of infectious
 FEs (301 cases), followed b...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5458897</comments>
            <pubDate>Mon, 28 Nov 2011 16:58:16 +0100</pubDate>
            <guid isPermaLink="false">5458897</guid>        </item>
        <item>
            <title>Spondylodiscitis from infection of central venous line inserted for haemophilia prophylaxis</title>
            <link>http://www.medworm.com/index.php?rid=5450094&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fw8j311l024184q66%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorPages 1-2DOI 10.1007/s00277-011-1374-1Authors
		Jecko Thachil, Department of Haematology, Roald Dahl Haemostasis and Thrombosis Centre, Royal Liverpool University Hospital, Liverpool, L7 8XP UKArvind Pillai, Department of Haematology, Roald Dahl Haemostasis and Thrombosis Centre, Royal Liverpool University Hospital, Liverpool, L7 8XP UKVanessa Martlew, Department of Haematology, Roald Dahl Haemostasis and Thrombosis Centre, Royal Liverpool University Hospital, Liverpool, L7 8XP UK
	

	
		Journal Annals of HematologyOnline ISSN 1432-0584Print ISSN 0939-5555 (Source: Annals of Hematology)</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5450094</comments>
            <pubDate>Wed, 23 Nov 2011 16:33:31 +0100</pubDate>
            <guid isPermaLink="false">5450094</guid>        </item>
        <item>
            <title>Lessons from an incidental diagnosis of paroxysmal nocturnal haemoglobinuria</title>
            <link>http://www.medworm.com/index.php?rid=5432453&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fd0k2688qk5511771%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorPages 1-2DOI 10.1007/s00277-011-1362-5Authors
		Jecko Thachil, Department of Haematology, Roald Dahl Haemostasis and Thrombosis Centre, Royal Liverpool University Hospital, L7 8XP, Liverpool, UKTim Webster, Department of Stroke Medicine, Royal Liverpool University Hospital, L7 8XP, Liverpool, UKRichard Kelly, Department of Haematology, Leeds Teaching Hospitals, Leeds, UKPeter Hillmen, Department of Haematology, Leeds Teaching Hospitals, Leeds, UKVanessa Martlew, Department of Haematology, Roald Dahl Haemostasis and Thrombosis Centre, Royal Liverpool University Hospital, L7 8XP, Liverpool, UKAnita Hill, Department of Haematology, Leeds Teaching Hospitals, Leeds, UK
	

	
		Journal Annals of HematologyOnline ISSN 1432-0584Print ISSN 0...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5432453</comments>
            <pubDate>Fri, 18 Nov 2011 07:01:22 +0100</pubDate>
            <guid isPermaLink="false">5432453</guid>        </item>
        <item>
            <title>Detection of SET-NUP214 rearrangement using multiplex reverse transcriptase-polymerase chain reaction (RT-PCR) in acute leukemias: a case report and literature review on a Korean case series</title>
            <link>http://www.medworm.com/index.php?rid=5432454&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv68872778pm103q6%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorPages 1-4DOI 10.1007/s00277-011-1366-1Authors
		Eun Young Lee, Department of Laboratory Medicine, Yonsei University College of Medicine, Seoul, Republic of KoreaTae Sung Park, Department of Laboratory Medicine, School of Medicine, Kyung Hee University, Seoul, Republic of KoreaMin Jin Kim, Department of Laboratory Medicine, School of Medicine, Kyung Hee University, Seoul, Republic of KoreaMyung Hee Chang, Department of Internal Medicine, National Health Insurance Corporation Ilsan Hospital, Goyang, Republic of KoreaEun Hae Cho, Greencross Reference Laboratory, Yongin, Republic of KoreaSeo-Jin Park, Department of Laboratory Medicine, Yonsei University College of Medicine, Seoul, Republic of KoreaJong Rak Choi, Department of Laborator...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5432454</comments>
            <pubDate>Fri, 18 Nov 2011 07:01:21 +0100</pubDate>
            <guid isPermaLink="false">5432454</guid>        </item>
        <item>
            <title>Genomic analysis of a four-way t(4;11;22;10) associated with MLL-AF4 in an adult acute lymphoblastic leukemia</title>
            <link>http://www.medworm.com/index.php?rid=5423192&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fbh82t5l2g6562523%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorPages 1-3DOI 10.1007/s00277-011-1364-3Authors
		Sun Young Cho, Department of Laboratory Medicine, Kyung Hee University School of Medicine, 1 Hoegi-dong, Dongdaemun-gu, Seoul, 130-702 South KoreaTae Sung Park, Department of Laboratory Medicine, Kyung Hee University School of Medicine, 1 Hoegi-dong, Dongdaemun-gu, Seoul, 130-702 South KoreaSeung Hwan Oh, Department of Laboratory Medicine, College of Medicine, Inje University, GaeGeum-dong, Busanjin-gu, Busan, 614-735 South KoreaEun Hae Cho, Greencross Reference Laboratory, 314 Bojeong-dong, Kiheung-gu, Yongin-city, Gyeonggi-do, South KoreaDoyeun Oh, Division of Hematology-Oncology, Department of Internal Medicine, CHA Bundang Medical Center, CHA University, Seongnam, Gyeonggi-do, Sou...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5423192</comments>
            <pubDate>Wed, 16 Nov 2011 06:50:33 +0100</pubDate>
            <guid isPermaLink="false">5423192</guid>        </item>
        <item>
            <title>Identification of patients with indolent B cell lymphoma sensitive to rituximab monotherapy</title>
            <link>http://www.medworm.com/index.php?rid=5423193&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl07m433tp4073784%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The potential predictive value of tumor bulk, genetic, and immunological variants in patients with low-grade non-Hodgkin's
 lymphoma to respond to treatment with rituximab (RTX) monotherapy was evaluated. Thus, the value of assessing the effect of
 18-fluoro-desoxy-d-glucose (FDG) uptake on PET scan, polymorphisms in Fc gamma receptor (FcγR) IIIa-158, FcγRIIa-131, and C1qA-276 genes in
 predicting the response to treatment were evaluated in 50 low-grade non-Hodgkin's lymphoma patients. The influence of RTX
 pharmacokinetics, plasma levels of the B cell-activating factor (BAFF), and human antichimeric antibodies was also investigated.
 The therapeutic response was evaluated 10&amp;nbsp;weeks after treatment using revised Cheson's criteria. Lower maximal standardized
 uptak...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5423193</comments>
            <pubDate>Tue, 15 Nov 2011 06:49:07 +0100</pubDate>
            <guid isPermaLink="false">5423193</guid>        </item>
        <item>
            <title>Course of serum 25-hydroxyvitamin D3 status and its influencing factors in adults undergoing allogeneic hematopoietic cell transplantation</title>
            <link>http://www.medworm.com/index.php?rid=5409613&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fpg0243530j725631%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Hypovitaminosis D (&amp;lt;30&amp;nbsp;ng/ml) is highly prevalent in allogeneic hematopoietic cell transplantation (alloHCT), but the relevance
 of influencing factors for serum 25-hydroxyvitamin D3 [25(OH)D3] status in adult patients remains unknown. We are the first to have prospectively assessed 25(OH)D3 status and its influencing factors in 102 patients before and at days +30 and +100 after alloHCT. Among others, we evaluated
 age, gender, weight, fat mass, season, sun exposure habits, and dietary and supplemental vitamin D intake as factors potentially
 influencing baseline vitamin D status in uni- and multivariate linear regression analysis. Furthermore, we investigated the
 impact of changes in fat mass, duration of parenteral nutrition, and acute graft-versus-host disea...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5409613</comments>
            <pubDate>Mon, 14 Nov 2011 06:35:24 +0100</pubDate>
            <guid isPermaLink="false">5409613</guid>        </item>
        <item>
            <title>Hemophagocytic syndrome associated with visceral leishmaniasis in an immunocompetent adult—case report and review of the literature</title>
            <link>http://www.medworm.com/index.php?rid=5409614&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe28hn30gwk566187%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorPages 1-3DOI 10.1007/s00277-011-1367-0Authors
		M. Koubâa, Department of Infectious Diseases, Hedi Chaker Hospital, Sfax, 3029 TunisiaI. Mâaloul, Department of Infectious Diseases, Hedi Chaker Hospital, Sfax, 3029 TunisiaCh Marrakchi, Department of Infectious Diseases, Hedi Chaker Hospital, Sfax, 3029 TunisiaM. Mdhaffar, Department of Clinic Hematology, Habib Bourguiba Hospital, Sfax, TunisiaD. Lahiani, Department of Infectious Diseases, Hedi Chaker Hospital, Sfax, 3029 TunisiaB. Hammami, Department of Infectious Diseases, Hedi Chaker Hospital, Sfax, 3029 TunisiaF. Makni, Department of Hematology, Hedi Chaker Hospital, Sfax, 3029 TunisiaA. Ayedi, Department of Parasitology, Habib Bourguiba Hospital, Sfax, TunisiaM. Ben Jemâa, De...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5409614</comments>
            <pubDate>Mon, 14 Nov 2011 06:35:23 +0100</pubDate>
            <guid isPermaLink="false">5409614</guid>        </item>
        <item>
            <title>A large family with MYH9 disorder caused by E1841K mutation suffering from serious kidney and hearing impairment and cataracts</title>
            <link>http://www.medworm.com/index.php?rid=5409615&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fw52kn846tj250847%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorPages 1-2DOI 10.1007/s00277-011-1370-5Authors
		Jihong Hao, Department of Clinical Laboratory, Second Hospital, Hebei Medical University, 215# Heping West Road, Shijiazhuang, 050000 ChinaShinji Kunishima, Department of Advanced Diagnosis, Clinical Research Center, National Hospital Organization Nagoya Medical Center, 4-1-1 Sannomaru, Naka-ku, Nagoya, 460-0001 JapanXin Guo, Department of Clinical Laboratory, Second Hospital, Hebei Medical University, 215# Heping West Road, Shijiazhuang, 050000 ChinaRui Hu, Department of Clinical Laboratory, Second Hospital, Hebei Medical University, 215# Heping West Road, Shijiazhuang, 050000 ChinaWeiguo Gao, Department of Clinical Laboratory, Hospital of Hebei Engineering University, Handan, China
...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5409615</comments>
            <pubDate>Mon, 14 Nov 2011 06:35:22 +0100</pubDate>
            <guid isPermaLink="false">5409615</guid>        </item>
        <item>
            <title>Extravascular hemolytic attack after eculizumab therapy for paroxysmal nocturnal hemoglobinuria</title>
            <link>http://www.medworm.com/index.php?rid=5409616&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F5w21437868477w77%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorPages 1-3DOI 10.1007/s00277-011-1368-zAuthors
		Akihiro Tomita, Department of Hematology and Oncology, Nagoya University Graduate School of Medicine, Tsurumai-cho 65, Showa-ku, Nagoya, 466-8550 JapanYukari Shirasugi, Department of Hematology and Oncology, Tokai University Hospital, Isehara, JapanTakahiko Ito, Department of Hematology, Gifu Social Insurance Hospital, Kani, JapanHisashi Tsurumi, First Department of Internal Medicine, Gifu University Graduate School of Medicine, Gifu, JapanTomoki Naoe, Department of Hematology and Oncology, Nagoya University Graduate School of Medicine, Tsurumai-cho 65, Showa-ku, Nagoya, 466-8550 Japan
	

	
		Journal Annals of HematologyOnline ISSN 1432-0584Print ISSN 0939-5555 (Source: Annals of Hema...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5409616</comments>
            <pubDate>Mon, 14 Nov 2011 06:35:20 +0100</pubDate>
            <guid isPermaLink="false">5409616</guid>        </item>
        <item>
            <title>Early engraftment of G-CSF-primed allogeneic bone marrow transplantation in pediatric patients regardless of donor–recipient weight differences</title>
            <link>http://www.medworm.com/index.php?rid=5409617&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn21g3373712t8728%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Harvesting sufficient progenitor cells from bone marrow (BM) for pediatric patients is a challenging process, especially from
 smaller donors. Growth factor administration to donors prior to harvest results in an enrichment of the graft and leads to
 early engraftment. A total of 41 patients received a human leukocyte antigen-identical sibling transplantation using granulocyte
 colony-stimulating factor (G-CSF)-primed BM. All donors received G-CSF 10&amp;nbsp;μg/kg/day for 2&amp;nbsp;days prior to harvest. The median
 weight difference between donor and recipient was 3.9&amp;nbsp;kg (range, −29.8 to 32&amp;nbsp;kg), and the median number of CD34+ cells harvested was 4.16 × 106/kg (range, 1.17–31.9 × 106/kg). The median time to neutrophil engraftment was 12&amp;nbsp;days (ran...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5409617</comments>
            <pubDate>Fri, 11 Nov 2011 06:54:34 +0100</pubDate>
            <guid isPermaLink="false">5409617</guid>        </item>
        <item>
            <title>Clinical significance of metabolic tumor volume by PET/CT in stages II and III of diffuse large B cell lymphoma without extranodal site involvement</title>
            <link>http://www.medworm.com/index.php?rid=5409618&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F65khg731k73875w3%2F</link>
            <description>The objective of this study was to investigate whether metabolic tumor volume (MTV) by positron emission tomography (PET)
 can be a potential prognostic tool when compared with Ann Arbor stage, in stages II and III nodal diffuse large B cell lymphoma
 (DLBCL). We evaluated 169 patients with nodal stages II and III DLBCL who underwent measurements with PET prior to rituximab
 combined with cyclophosphamide, adriamycin, vincristine, and prednisone (R-CHOP). Cutoff point of MTV was measured using the
 receiver operating characteristic (ROC) curve. During a median period of 36&amp;nbsp;months, stage II was 59.2% and III was 40.8%.
 Using the ROC curve, the MTV of 220&amp;nbsp;cm3 was the cutoff value. The low MTV group (&amp;lt;220&amp;nbsp;cm3) had longer progression-free survival (PFS) and overall survival ...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5409618</comments>
            <pubDate>Thu, 10 Nov 2011 06:46:30 +0100</pubDate>
            <guid isPermaLink="false">5409618</guid>        </item>
        <item>
            <title>Efficacy and safety of oral deferasirox treatment in the posttransplant period for patients who have undergone allogeneic hematopoietic stem cell transplantation (alloHSCT)</title>
            <link>http://www.medworm.com/index.php?rid=5388863&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fht5t5764t254t0t5%2F</link>
            <description>In conclusion, our data suggest that oral deferasirox treatment
 may be used as a safe and effective alternative method for reducing iron overload in alloHSCT recipients, whether combined
 with or without phlebotomy.
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-7DOI 10.1007/s00277-011-1358-1Authors
		Serdar Sivgin, Stem Cell Transplantation Hospital, Department of Hematology, Faculty of Medicine, Erciyes University, Kayseri, 38039 TurkeyBulent Eser, Stem Cell Transplantation Hospital, Department of Hematology, Faculty of Medicine, Erciyes University, Kayseri, 38039 TurkeySami Bahcebasi, Stem Cell Transplantation Hospital, Department of Hematology, Faculty of Medicine, Erciyes University, Kayseri, 38039 TurkeyLeylagul Kaynar, Stem Cell Transplantation Hospital, Departme...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5388863</comments>
            <pubDate>Thu, 03 Nov 2011 16:55:07 +0100</pubDate>
            <guid isPermaLink="false">5388863</guid>        </item>
        <item>
            <title>Human herpesvirus 6 in biopsies from patients with gastrointestinal symptoms after allogeneic stem cell transplantation</title>
            <link>http://www.medworm.com/index.php?rid=5388865&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fmx4433170215n75h%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Gastrointestinal complications are frequent after allogeneic stem cell transplantation (allo-SCT). Main differential diagnoses
 are graft-versus-host disease (GvHD) and viral infections. In this retrospective analysis, we included 50 patients with severe
 vomiting or diarrhea in the first year after allo-SCT. One hundred two biopsies obtained by colonoscopy or endoscopy of the
 upper gastrointestinal tract were analysed by conventional histology for signs of GvHD and by qualitative polymerase chain
 reaction (PCR) for viral DNA of human herpesvirus 6 (HHV-6) and other virus of the herpes family. DNA of HHV-6 was detected
 in 38 of 75 initial samples (51%) and in 19 of 27 follow-up biopsies (70%). In the initial samples (n = 75), HHV-6 DNA was detected in 20/37 (54%)...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5388865</comments>
            <pubDate>Wed, 02 Nov 2011 16:58:15 +0100</pubDate>
            <guid isPermaLink="false">5388865</guid>        </item>
        <item>
            <title>Good adherence to imatinib therapy among patients with chronic myeloid leukemia—a single-center observational study</title>
            <link>http://www.medworm.com/index.php?rid=5388864&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fwmt6h1154776ln20%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Previous studies have suggested that adherence to imatinib therapy can be an obstacle among patients with chronic myeloid
 leukemia (CML). We studied adherence to imatinib therapy among CML patients treated at the Sahlgrenska University Hospital.
 We identified all CML patients that were alive at the 1st of January 2010 (n = 70). Nineteen patients were excluded due to a history of allogenic hematopoietic stem cell transplantation, and nine were
 excluded due to treatment with other tyrosine kinase inhibitors. Thirty-eight out of 42 patients (90%) treated with imatinib
 accepted inclusion in the study. The patients were interviewed in a structured way, and adherence was evaluated in a standardized
 way using the nine-item Morisky Medication Adherence Scale that range...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5388864</comments>
            <pubDate>Wed, 02 Nov 2011 16:58:15 +0100</pubDate>
            <guid isPermaLink="false">5388864</guid>        </item>
        <item>
            <title>Single nucleotide polymorphism of Wilms’ tumor 1 gene rs16754 in Korean patients with cytogenetically normal acute myeloid leukemia</title>
            <link>http://www.medworm.com/index.php?rid=5349002&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe0275307096t352q%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A recent study from Germany showed that WT1 single nucleotide polymorphism (SNP) rs16754 was an independent prognostic factor in cytogenetically normal acute myeloid
 leukemia (CN-AML). We analyzed clinical impact of the WT1 rs16754 genotype on disease characteristics and outcomes in Korean patients with CN-AML. A total of 73 patients with CN-AML
 were included in the study. All patients received standard induction chemotherapy and their bone marrow or peripheral blood
 samples were cryopreserved at the time of diagnosis. WT1 exons 7 and 9 were amplified using polymerase chain reaction and directly sequenced. The genotype frequency for WT1 rs16754 was 6.8% for AA, 39.7% for GA, and 53.4% for GG. G was a minor allele in German population, whereas it was a major
 allele i...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5349002</comments>
            <pubDate>Thu, 20 Oct 2011 15:53:57 +0100</pubDate>
            <guid isPermaLink="false">5349002</guid>        </item>
        <item>
            <title>Role of FDG-PET/CT in detecting lymphomatous bone marrow involvement in patients with newly diagnosed diffuse large B-cell lymphoma</title>
            <link>http://www.medworm.com/index.php?rid=5337256&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fxpp6424m03x35366%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;To evaluate the role of FDG-PET/CT in detecting bone marrow (BM) involvement, pre-treatment bilateral bone marrow biopsies
 (BMBs) and FDG-PET/CT scans of 89 patients with diffuse large B-cell lymphoma (DLBCL) treated with rituximab–CHOP were reviewed
 and analyzed. Fourteen patients (15.7%) had lymphomatous involvement based on BMB (BMB+), and 17 patients (19.1%) had the
 possibility of BM involvement on FDG-PET/CT (FDG-PET/CT+). Seventy-two patients (80.8%) had concordant results between BMB
 and FDG-PET/CT (seven patients were positive for both, and 65 patients were negative for both), but 17 patients (19.2%) had
 a discordant interpretation (seven patients were BMB+ and FDG-PET/CT−, and ten were BMB− and FDG-PET/CT+). Although BMB+ patients
 had an inferior 2-...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5337256</comments>
            <pubDate>Tue, 18 Oct 2011 15:58:56 +0100</pubDate>
            <guid isPermaLink="false">5337256</guid>        </item>
        <item>
            <title>Extensive bone marrow amyloidosis</title>
            <link>http://www.medworm.com/index.php?rid=5337257&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl4747632w4628572%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorPages 1-2DOI 10.1007/s00277-011-1356-3Authors
		Stefano Licci, Department of Pathology, “Santo Spirito” Hospital, Lungotevere in Sassia, 1, 00193 Rome, Italy
	

	
		Journal Annals of HematologyOnline ISSN 1432-0584Print ISSN 0939-5555 (Source: Annals of Hematology)</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5337257</comments>
            <pubDate>Mon, 17 Oct 2011 16:04:53 +0100</pubDate>
            <guid isPermaLink="false">5337257</guid>        </item>
        <item>
            <title>Cytomegalovirus infection and disease after allogeneic hematopoietic stem cell transplantation: experience in a center with a high seroprevalence of both CMV and hepatitis B virus</title>
            <link>http://www.medworm.com/index.php?rid=5324644&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fr2366346u2w51393%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Cytomegalovirus (CMV) infection and disease are important concerns after allogeneic hematopoietic stem cell transplantation
 (allo-HSCT). The similarity of hepatitis B virus (HBV) and CMV with regards to their chronic viral persistence and potential
 reactivation at the time of impaired cellular immunity has raised clinicians’ interest in the occurrence and association between
 them among patients receiving allo-HSCT; however, only limited data have been obtained from a high seroprevalence region of
 both CMV and HBV. We monitored 117 adult allo-HSCT patients with both CMV polymerase chain reaction and pp65 antigenemia assay
 weekly until day 100. In 91.8% of our cases, donors and recipients were both CMV seropositive, and 13.7% of the patients were
 positive for HBV ...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5324644</comments>
            <pubDate>Fri, 14 Oct 2011 06:09:45 +0100</pubDate>
            <guid isPermaLink="false">5324644</guid>        </item>
        <item>
            <title>IDH1 and IDH2 mutation analysis in Chinese patients with acute myeloid leukemia and myelodysplastic syndrome</title>
            <link>http://www.medworm.com/index.php?rid=5324645&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fy519hj3135205q55%2F</link>
            <description>In conclusion, IDH1/2 mutations are recurrent but rare molecular aberrations in Chinese
 AML and MDS.
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-7DOI 10.1007/s00277-011-1352-7Authors
		Jiang Lin, Laboratory Center, Affiliated People’s Hospital of Jiangsu University, Zhenjiang, Jiangsu 212002, People’s Republic of ChinaDong-ming Yao, Laboratory Center, Affiliated People’s Hospital of Jiangsu University, Zhenjiang, Jiangsu 212002, People’s Republic of ChinaJun Qian, Department of Hematology, Affiliated People’s Hospital of Jiangsu University, 8 Dianli Rd., 212002 Zhenjiang, Jiangsu, People’s Republic of ChinaQin Chen, Department of Hematology, Affiliated People’s Hospital of Jiangsu University, 8 Dianli Rd., 212002 Zhenjiang, Jiangsu, People’s Republic ...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5324645</comments>
            <pubDate>Thu, 13 Oct 2011 15:47:04 +0100</pubDate>
            <guid isPermaLink="false">5324645</guid>        </item>
        <item>
            <title>Microscopic examination of bone marrow aspirates in malignant disorders of haematopoiesis—a comparison of two slide preparation techniques</title>
            <link>http://www.medworm.com/index.php?rid=5316371&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F0p244l18310761u3%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;It is mandatory to perform microscopic examinations of bone marrow aspirates during the diagnosis of many neoplastic haematopoiesis
 disorders. In 2008, The International Committee for Standardization in Hematology recommended the use of two types of slides
 for the microscopic evaluation of bone marrow: wedge-spread film and crush film slides. Because these techniques have not
 yet been compared, we performed such a comparison. Routine bone marrow samples from 250 patients diagnosed due to different
 neoplastic haematological disorders were evaluated. The major differences between the two compared techniques were identified
 in 13 patients with non-Hodgkin’s lymphoma, seven patients with systemic mastocytosis and 11 patients with acute leukaemias
 or myelodysplastic ...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5316371</comments>
            <pubDate>Tue, 11 Oct 2011 15:53:26 +0100</pubDate>
            <guid isPermaLink="false">5316371</guid>        </item>
        <item>
            <title>Serum microRNAs are promising novel biomarkers for diffuse large B cell lymphoma</title>
            <link>http://www.medworm.com/index.php?rid=5316372&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fy02u6847786636w4%2F</link>
            <description>In conclusion, these data suggest that serum miRNAs are potentially useful tools as novel noninvasive biomarker for
 the diagnosis of DLBCL.
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-7DOI 10.1007/s00277-011-1350-9Authors
		Cheng Fang, Department of Hematology, The First Affiliated Hospital of Nanjing Medical University, Jiangsu Province Hospital, 300 Guangzhou Road, Nanjing, 210029 ChinaDan-Xia Zhu, Department of Hematology, The First Affiliated Hospital of Nanjing Medical University, Jiangsu Province Hospital, 300 Guangzhou Road, Nanjing, 210029 ChinaHua-Jie Dong, Department of Hematology, The First Affiliated Hospital of Nanjing Medical University, Jiangsu Province Hospital, 300 Guangzhou Road, Nanjing, 210029 ChinaZhi-Jian Zhou, Department of Hematology, The Firs...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5316372</comments>
            <pubDate>Mon, 10 Oct 2011 15:05:05 +0100</pubDate>
            <guid isPermaLink="false">5316372</guid>        </item>
        <item>
            <title>Secondary haematological malignancies after radioimmunotherapy</title>
            <link>http://www.medworm.com/index.php?rid=5316373&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fxh6623437m5j8246%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorPages 1-1DOI 10.1007/s00277-011-1345-6Authors
		Federica Gigli, European Institute of Oncology—Division of Hematoncology, Milan, ItalyAngelo Gardellini, European Institute of Oncology—Division of Hematoncology, Milan, ItalyPaola Bertazzoni, European Institute of Oncology—Division of Hematoncology, Milan, ItalyGiovanni Martinelli, European Institute of Oncology—Division of Hematoncology, Milan, Italy
	

	
		Journal Annals of HematologyOnline ISSN 1432-0584Print ISSN 0939-5555 (Source: Annals of Hematology)</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5316373</comments>
            <pubDate>Mon, 10 Oct 2011 15:05:04 +0100</pubDate>
            <guid isPermaLink="false">5316373</guid>        </item>
        <item>
            <title>Evaluation of circulating soluble triggering receptor expressed on myeloid cells-1 (sTREM-1) to predict risk profile, response to antimicrobial therapy, and development of complications in patients with chemotherapy-associated febrile neutropenia: a pilot study</title>
            <link>http://www.medworm.com/index.php?rid=5305188&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F500317722344v740%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The soluble triggering receptor expressed on myeloid cells 1 (sTREM-1) is a useful marker of infection in patients with sepsis,
 but has not been adequately evaluated in patients with chemotherapy-associated febrile neutropenia (FN). The value of sTREM-1
 in this setting has been tested in a retrospective, pilot study using stored serum from 48 cancer patients with documented
 FN. On presentation, patients were categorized according to the Talcott risk-index clinical score. Circulating soluble sTREM-1
 was measured using an ELISA procedure, while procalcitonin (PCT) or interleukins 6 (IL-6) and 8 (IL-8), included for comparison,
 were measured using an immunoluminescence-based assay and Bio-Plex® suspension bead array system, respectively. Circulating
 concentrations o...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5305188</comments>
            <pubDate>Thu, 06 Oct 2011 05:49:29 +0100</pubDate>
            <guid isPermaLink="false">5305188</guid>        </item>
        <item>
            <title>Successful transfusion care for a patient with the Rhesus -D- phenotype and antibodies against Rh17 and two additional alloantibodies</title>
            <link>http://www.medworm.com/index.php?rid=5305187&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fw4177k07750475g8%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorPages 1-2DOI 10.1007/s00277-011-1344-7Authors
		Karen M. K. De Vooght, Department of Clinical Chemistry and Haematology, University Medical Center Utrecht, Postbus 85500, 3508 GA Utrecht, The NetherlandsAyşe Y. Demir, Department of Clinical Chemistry and Haematology, Meander Medical Center, Amersfoort, The NetherlandsClaudia C. Folman, Sanquin Diagnostic Services, Amsterdam, The NetherlandsRoger E. G. Schutgens, Department of Haematology/Van Creveldkliniek, University Medical Center Utrecht, Utrecht, The NetherlandsWouter W. van Solinge, Department of Clinical Chemistry and Haematology, University Medical Center Utrecht, Postbus 85500, 3508 GA Utrecht, The NetherlandsHans Kemperman, Department of Clinical Chemistry and Haematology...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5305187</comments>
            <pubDate>Thu, 06 Oct 2011 05:49:29 +0100</pubDate>
            <guid isPermaLink="false">5305187</guid>        </item>
        <item>
            <title>Vincristine-induced vocal cord paralysis in a patient with acute lymphoblastic leukemia</title>
            <link>http://www.medworm.com/index.php?rid=5305189&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu41561048x2m2263%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorPages 1-2DOI 10.1007/s00277-011-1348-3Authors
		Larry C. Bacon, Leukemia/Bone Marrow Transplant Program of British Columbia, British Columbia Cancer Agency, Vancouver, BC, CanadaMichael J. Barnett, Leukemia/Bone Marrow Transplant Program of British Columbia, British Columbia Cancer Agency, Vancouver, BC, CanadaYasser R. Abou Mourad, Leukemia/Bone Marrow Transplant Program of British Columbia, British Columbia Cancer Agency, Vancouver, BC, Canada
	

	
		Journal Annals of HematologyOnline ISSN 1432-0584Print ISSN 0939-5555 (Source: Annals of Hematology)</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5305189</comments>
            <pubDate>Thu, 06 Oct 2011 05:49:27 +0100</pubDate>
            <guid isPermaLink="false">5305189</guid>        </item>
        <item>
            <title>Case-matched comparison with standard versus reduced intensity conditioning regimen in chronic myeloid leukemia patients</title>
            <link>http://www.medworm.com/index.php?rid=5297772&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv6u2364tx1r074l5%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;This retrospective case-matched study evaluated the efficacy of reduced intensity conditioning (RIC) regimen on early and
 late allogeneic transplant outcome in chronic myeloid leukemia (CML) patients. Twenty-eight patients conditioned with RIC
 regimen were matched to 56 patients who received a myeloablative conditioning (MAC) regimen. The main criteria for case matching
 among our CML allotransplant cohort were the Gratwohl scoring system. The median score was 2 (1–4) in each group. The pretransplant
 disease status was first chronic phase (CP1, n = 20), CP2 (n = 2), and advanced phase (n = 6) in RIC, and CP1 (n = 46), CP2 (n = 3), and advanced phase (n = 7) in MAC. The duration of neutropenia and thrombocytopenia was shorter in RIC than MAC....</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5297772</comments>
            <pubDate>Wed, 05 Oct 2011 05:49:35 +0100</pubDate>
            <guid isPermaLink="false">5297772</guid>        </item>
        <item>
            <title>Mild hepatic iron overload in dysmetabolic hyperferritinemia: MRI may overestimate the liver iron concentration values</title>
            <link>http://www.medworm.com/index.php?rid=5297771&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F53716jx65t765tvm%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorPages 1-1DOI 10.1007/s00277-011-1346-5Authors
		Agustin Castiella, Gastroenterology, Mendaro Hospital, Mendaro, Gipuzkoa, SpainJose M. Alustiza, Osatek, Radiology Service, Donostia Hospital, San Sebastián, Gipuzkoa, SpainEva Zapata, Gastroenterology, Mendaro Hospital, Mendaro, Gipuzkoa, SpainJose I. Emparanza, Clinical Epidemiology Unit. Casp-e, CIBER-ESP, San Sebastián, Gipuzkoa, SpainPedro Otazua, Gastroenterology, Mondragon Hospital, Paiz Vasco, SpainLeire Zubiaurre, Gastroenterology, Mendaro Hospital, Mendaro, Gipuzkoa, SpainAlazne Aguirre, Gastroenterology, Mendaro Hospital, Mendaro, Gipuzkoa, Spain
	

	
		Journal Annals of HematologyOnline ISSN 1432-0584Print ISSN 0939-5555 (Source: Annals of Hematology)</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5297771</comments>
            <pubDate>Wed, 05 Oct 2011 05:49:35 +0100</pubDate>
            <guid isPermaLink="false">5297771</guid>        </item>
        <item>
            <title>Quality of life in elderly patients with essential thrombocythaemia. An Italian multicentre study</title>
            <link>http://www.medworm.com/index.php?rid=5286670&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fbk08221u64472350%2F</link>
            <description>In conclusion, physicians should take into consideration PROs, as “attitude” is associated with physical and mental
 QoL. Treatment should be tailored to patients’ needs according to comorbidities, lifestyle, and psychological conditions.
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-6DOI 10.1007/s00277-011-1341-xAuthors
		Esther Natalie Oliva, Hematology Unit, Azienda Ospedaliera “Bianchi-Melacrino-Morelli”, Reggio Calabria, ItalyAndrea Piccin, Department of Haematology, San Maurizio Regional Hospital, Bolzano, ItalyMaria Gabriella Mazzucconi, Hematology, “Dipartimento di Biotecnologie Cellulari ed Ematologia, “Sapienza” University of Rome, Rome, ItalyEnrica Morra, Hematology Division and UTMO, Ospedale Niguarda Ca’ Granda, Milan, ItalyUmberto Recine,...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5286670</comments>
            <pubDate>Sat, 01 Oct 2011 05:45:10 +0100</pubDate>
            <guid isPermaLink="false">5286670</guid>        </item>
        <item>
            <title>Immune response as a possible mechanism of long-lasting disease control in spontaneous remission of MLL/AF9-positive acute myeloid leukemia</title>
            <link>http://www.medworm.com/index.php?rid=5286671&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fy414n81756545v63%2F</link>
            <description>We describe the
 10-year follow-up of a patient with MLL-AF9-positive AML (Müller et al. Eur J Haematol 73:62–66, 2004), including ex vivo antileukemic immune responses which may contribute to the long-lasting spontaneous CR (tantamount to
 cure). We could demonstrate strong in vitro cytotoxic activity mediated by the patient’s serum (cryopreserved at diagnosis
 2001) against myeloid cell lines. We also addressed cellular cytotoxic activity against myeloid leukemia cells. When the patient’s
 natural killer (NK) cells (obtained in 2007) were tested against the K562 cell line, upregulation of CD107 occurred, implying
 that long-term CR in this patient could be due to NK cell-mediated disease control.
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-6DOI 10.1007/s00277...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5286671</comments>
            <pubDate>Fri, 30 Sep 2011 05:54:03 +0100</pubDate>
            <guid isPermaLink="false">5286671</guid>        </item>
        <item>
            <title>Athrombogenic coating of long-term venous catheter for cancer patients: a prospective, randomised, double-blind trial</title>
            <link>http://www.medworm.com/index.php?rid=5286672&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj1121q8p6866r201%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Cancer patients with long-term venous catheter are at risk for thromboembolic complications at the catheter tip and in the
 adjacent venous vessels. We assessed whether local thrombogenicity could be prevented with an experimental coated (with athrombogenic
 layer) catheter device (CD) compared to an uncoated CD. Patients requiring a long-term venous catheter were randomly allocated
 to receive either a standard uncoated or experimental coated (with athrombogenic Camouflage® layer) CD. The athrombogenic
 layer creates a barrier against non-specific adsorption of plasma proteins. The primary endpoint was urokinase injection in
 cases of an unsuccessful blood aspiration from the CD. Secondary endpoints included early (haematoma, pneumothorax) and late
 (venous thrombosis...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5286672</comments>
            <pubDate>Thu, 29 Sep 2011 06:18:25 +0100</pubDate>
            <guid isPermaLink="false">5286672</guid>        </item>
        <item>
            <title>Oxidative stress and antioxidant capacity in sickle cell anaemia patients receiving different treatments and medications for different periods of time</title>
            <link>http://www.medworm.com/index.php?rid=5274848&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F730q5n047462v701%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;To evaluate, in a longitudinal study, the profile of lipid peroxidation and antioxidant capacity markers in sickle cell anaemia
 patients receiving different treatments and medication over different time periods. The three groups were: patients undergoing
 transfusion therapy and receiving iron chelator deferasirox (DFX group, n = 20); patients receiving deferasirox and hydroxyurea (DFX + HU group, n = 10), and patients receiving only folic acid (FA group, n = 15). Thiobarbituric acid-reactive substance (TBARS) assays and trolox-equivalent antioxidant capacity (TEAC) assays were
 evaluated during two different periods of analysis, T0 and T1 (after ~388&amp;nbsp;days). Higher FA group TBARS values were observed
 compared with the DFX + HU group (p = 0.016) at...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5274848</comments>
            <pubDate>Tue, 27 Sep 2011 06:18:17 +0100</pubDate>
            <guid isPermaLink="false">5274848</guid>        </item>
        <item>
            <title>Prevalence of C282Y, H63D, and S65C mutations in hereditary HFE-hemochromatosis gene in Lithuanian population</title>
            <link>http://www.medworm.com/index.php?rid=5274847&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ffn8494654150115k%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;
 HFE-hemochromatosis is a common autosomal recessive disease caused by HFE gene mutations and characterized as iron overload and failure of different organs. The aim of this study was to determine
 the prevalence of C282Y (c.845&amp;nbsp;G &amp;gt; A), H63D (c.187&amp;nbsp;C &amp;gt; G), and S65C (c.193A &amp;gt; T) alleles of HFE gene in the Lithuanian population. One thousand and eleven healthy blood donors of Lithuanian nationality were examined in
 four different ethnic Lithuanian regions to determine HFE gene alleles and genotype frequencies. The samples of DNA were analyzed for the presence of restriction fragment length polymorphism
 and validated by DNA sequencing. Among 1,011 blood donors tested, the frequency of C282Y, H63D, and S65C alleles were 2.6%,
 15.9%, and 1....</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5274847</comments>
            <pubDate>Tue, 27 Sep 2011 06:18:17 +0100</pubDate>
            <guid isPermaLink="false">5274847</guid>        </item>
        <item>
            <title>Pilot study on combination of azacitidine and low-dose cytarabine for patients with refractory anemia with excess blast</title>
            <link>http://www.medworm.com/index.php?rid=5274849&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe8151677301336jk%2F</link>
            <description>This study analyzed the outcomes of the combination of azacitidine and low-dose cytarabine in patients newly diagnosed with
 refractory anemia with excess blast (RAEB). Patients were treated with azacitidine 75&amp;nbsp;mg/m2 for 7&amp;nbsp;days subcutaneously and cytarabine 20&amp;nbsp;mg/m2 intravenously for 7&amp;nbsp;days every 28&amp;nbsp;days. The assigned regimen was repeated for two cycles, then the patients treated with
 azacytidine alone until progression or allogeneic stem cell transplantation (allo-SCT). Eighteen patients with 5 RAEB-1 and
 13 RAEB-2 were enrolled in the current study. After two cycles of the combination therapy, responses were achieved in nine
 patients (50.0%): four complete response (CR) (22.2%), one partial response (5.6%), two marrow-CR (11.1%), and two hematologic
 improveme...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5274849</comments>
            <pubDate>Tue, 27 Sep 2011 06:18:16 +0100</pubDate>
            <guid isPermaLink="false">5274849</guid>        </item>
        <item>
            <title>High hyperdiploid acute lymphoblastic leukemia in adults shows clonal heterogeneity and chromosomal instability at diagnosis and during the course of the disease</title>
            <link>http://www.medworm.com/index.php?rid=5251559&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl44582n5l7h68725%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorPages 1-4DOI 10.1007/s00277-011-1317-xAuthors
		Anna Talamo, Cancer Cytogenetics Unit, Medical Genetics Service, University Hospital and University of Lausanne (CHUV-UNIL), Lausanne, SwitzerlandAlfio Marazzi, Institute of Social and Preventive Medicine, University of Lausanne, Lausanne, SwitzerlandAlicia Rovo, Hematology Department, University Hospital of Basel, Basel, SwitzerlandUrs Schanz, Department of Hematology, University Hospital of Zurich, Zurich, SwitzerlandAndré Tichelli, Hematology Department, University Hospital of Basel, Basel, SwitzerlandYves Chalandon, Hematology Division, University Hospital of Geneva (HUG), Geneva, SwitzerlandMartine Jotterand, Medical Genetics Service, University Hospital and University of Lausan...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5251559</comments>
            <pubDate>Fri, 23 Sep 2011 05:41:42 +0100</pubDate>
            <guid isPermaLink="false">5251559</guid>        </item>
        <item>
            <title>Anemia and global iron fortification and supplementation</title>
            <link>http://www.medworm.com/index.php?rid=5251560&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb706773775465510%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorPages 1-2DOI 10.1007/s00277-011-1335-8Authors
		Andrew J. Ghio, Environmental Public Health Division, National Health and Environmental Effects Research Laboratory, US Environmental Protection Agency, Chapel Hill, NC, USA
	

	
		Journal Annals of HematologyOnline ISSN 1432-0584Print ISSN 0939-5555 (Source: Annals of Hematology)</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5251560</comments>
            <pubDate>Thu, 22 Sep 2011 05:51:18 +0100</pubDate>
            <guid isPermaLink="false">5251560</guid>        </item>
        <item>
            <title>Follicular lymphoma with prominent fibrosis complicated by peripheral eosinophilia</title>
            <link>http://www.medworm.com/index.php?rid=5251561&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ftv530x0134q20681%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorPages 1-3DOI 10.1007/s00277-011-1342-9Authors
		Rie Tabata, Department of Internal Medicine, Hyogo Prefectural Tsukaguchi Hospital, 6-8-17 Minamitsukaguchi, Amagasaki, Hyogo 661-0012, JapanChiharu Tabata, Division of Respiratory Medicine, Department of Internal Medicine, Hyogo College of Medicine, Hyogo, JapanTomoko Nagai, Department of Internal Medicine, Hyogo Prefectural Tsukaguchi Hospital, 6-8-17 Minamitsukaguchi, Amagasaki, Hyogo 661-0012, JapanRyoji Yasumizu, Division of Pathology, Hyogo Prefectural Tsukaguchi Hospital, Hyogo, Japan
	

	
		Journal Annals of HematologyOnline ISSN 1432-0584Print ISSN 0939-5555 (Source: Annals of Hematology)</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5251561</comments>
            <pubDate>Thu, 22 Sep 2011 05:51:17 +0100</pubDate>
            <guid isPermaLink="false">5251561</guid>        </item>
        <item>
            <title>Is obesity a prognostic factor for acute myeloid leukemia outcome?</title>
            <link>http://www.medworm.com/index.php?rid=5251562&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg869p224u71gg406%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Obesity adversely affects outcome in pediatric acute lymphocytic leukemia and acute myeloid leukemia (AML). We asked if obesity,
 measured by body mass index (BMI), affected outcome in 329 adult AML patients treated with high-dose cytarabine and idarubicin-containing
 regimens administered according to actual body weight. Age ≥ 60, unfavorable karyotype, secondary AML, and positive smoking
 status had adverse impact on overall survival in a multivariate analysis, while BMI did not. We conclude that high BMI should
 not be a barrier to administer high-dose cytarabine-containing regimens for AML induction.
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-7DOI 10.1007/s00277-011-1319-8Authors
		Hun Ju Lee, Leukemia Section, Department of Medicine, Ro...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5251562</comments>
            <pubDate>Wed, 21 Sep 2011 05:53:12 +0100</pubDate>
            <guid isPermaLink="false">5251562</guid>        </item>
        <item>
            <title>Prognostic value of cytogenetics in adult patients with Philadelphia-negative acute lymphoblastic leukemia</title>
            <link>http://www.medworm.com/index.php?rid=5251563&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F032w302422x07556%2F</link>
            <description>In conclusion, karyotype is a useful tool for risk assessment in adult ALL. We have confirmed the bad prognosis of t(4;11)(q21;q23)/MLL/AF4
 and hypodiploidy. Besides, low hyperdiploidy could also define a high-risk group of patients who might be candidates for more
 intensive treatment.
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-7DOI 10.1007/s00277-011-1331-zAuthors
		Inés Gómez-Seguí, Department of Hematology, Hospital Universitario La Fe, Valencia, SpainJose Cervera, Department of Hematology, Hospital Universitario La Fe, Valencia, SpainEsperanza Such, Department of Hematology, Hospital Universitario La Fe, Valencia, SpainDavid Martínez-Cuadrón, Department of Hematology, Hospital Universitario La Fe, Valencia, SpainIrene Luna, Department of Hematology, Hospit...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5251563</comments>
            <pubDate>Wed, 21 Sep 2011 05:53:11 +0100</pubDate>
            <guid isPermaLink="false">5251563</guid>        </item>
        <item>
            <title>Phase II trial of rituximab plus CVP combination chemotherapy for advanced stage marginal zone lymphoma as a first-line therapy: Consortium for Improving Survival of Lymphoma (CISL) study</title>
            <link>http://www.medworm.com/index.php?rid=5227228&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fw3x01p28762j4330%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;We conducted a multicenter, phase II trial to investigate the efficacy and safety of rituximab plus CVP (R-CVP) combination
 therapy for patients with previously untreated stage III or IV marginal zone lymphoma (MZL). The treatment consisted of rituximab
 375&amp;nbsp;mg/m2, cyclophosphamide 750&amp;nbsp;mg/m2 and vincristine 1.4&amp;nbsp;mg/m2 (maximum 2.0&amp;nbsp;mg) being given intravenously on day 1 and oral prednisolone 100&amp;nbsp;mg on days 1–5. The treatment was repeated
 every 3&amp;nbsp;weeks and this was continued for six or eight cycles. Forty-two patients were enrolled from 13 institutes in Korea.
 Among them, two patients were dropped after the first and second cycles of chemotherapy, respectively, without evaluation.
 The 40 patients received a total of 287 cycles of R-CVP c...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5227228</comments>
            <pubDate>Thu, 15 Sep 2011 15:50:34 +0100</pubDate>
            <guid isPermaLink="false">5227228</guid>        </item>
        <item>
            <title>A composite small lymphocytic lymphoma and Hodgkin transformation presenting as acute appendicitis</title>
            <link>http://www.medworm.com/index.php?rid=5227229&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ff3844816p1q50620%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorPages 1-2DOI 10.1007/s00277-011-1323-zAuthors
		Brian Quigley, Department of Pathology and Cell Biology, University of South Florida College of Medicine, 4105 W Coachman Ave, Tampa, FL 33611, USADeniz Peker, Department of Hematopathology and Laboratory Medicine, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USALing Zhang, Department of Hematopathology and Laboratory Medicine, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USA
	

	
		Journal Annals of HematologyOnline ISSN 1432-0584Print ISSN 0939-5555 (Source: Annals of Hematology)</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5227229</comments>
            <pubDate>Tue, 13 Sep 2011 15:44:37 +0100</pubDate>
            <guid isPermaLink="false">5227229</guid>        </item>
        <item>
            <title>The time-dependent autophagy protects against apoptosis with possible involvement of Sirt1 protein in multiple myeloma under nutrient depletion</title>
            <link>http://www.medworm.com/index.php?rid=5227230&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fx47xh8w3nq8m6x47%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The absence of researches about autophagy in multiple myeloma promoted us to explore the biological characteristics and role
 of autophagy induced by nutrient depletion in multiple myeloma (MM) cell line RPMI8226 cells. Both autophagic and apoptotic
 morphology were observed by TUNEL, transmission electron microscopy (TEM), and monodansylcadervarine (MDC) staining. MDC staining
 fluorescent intensity and the conversion of LC3-I to LC3-II demonstrated autophagy increased time-dependently at 6, 12, and
 18&amp;nbsp;h then declined at 24 and 48&amp;nbsp;h. FCM analysis of Annexin V-FITC/PI (AV/PI) dual staining and TUNEL assay demonstrated apoptosis
 increased time-dependently at 6, 12, 18, 24, and 48&amp;nbsp;h, and it burst at 24&amp;nbsp;h when autophagy declined. Bax translocation fro...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5227230</comments>
            <pubDate>Tue, 13 Sep 2011 15:44:36 +0100</pubDate>
            <guid isPermaLink="false">5227230</guid>        </item>
        <item>
            <title>Cytomegalovirus infection is associated with venous thromboembolism of immunocompetent adults—a case–control study</title>
            <link>http://www.medworm.com/index.php?rid=5227231&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F2828726444545613%2F</link>
            <description>This study aimed to
 investigate if cytomegalovirus infection contributes to the development of VTE in immunocompetent individuals. CMV-IgG and
 CMV-IgM antibody titres, CMV-IgG avidity and CMV-DNA were identified in samples from 166 VTE patients and from 166 healthy
 blood donors matched for gender and age. CMV-IgG antibodies were found more frequently in VTE patients compared to controls
 [57.8% vs. 44.0%; adjusted OR 1.75 (95% CI 1.13–2.70); p = 0.016]. Accordingly, median CMV-IgG titres were significantly higher in the case group (89.4 vs. 1.8&amp;nbsp;AU/ml; p = 0.002). Although the overall rate was low, CMV-IgM antibodies were detected more often among cases than controls. The difference
 was significant in patients with an unprovoked VTE event [7.4% vs. 0.6%; adjusted OR 5.26 ...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5227231</comments>
            <pubDate>Mon, 12 Sep 2011 15:53:00 +0100</pubDate>
            <guid isPermaLink="false">5227231</guid>        </item>
        <item>
            <title>DAAM2 polymorphism is closely related to the clinical outcomes of allogeneic hematopoietic stem cell transplantation</title>
            <link>http://www.medworm.com/index.php?rid=5210165&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm131758k86q23m51%2F</link>
            <description>This study
 investigated the association of DAAM2 genetic polymorphism with the clinical outcomes of allogeneic hematopoietic stem cell transplantation (HSCT). We selected
 candidate single nucleotide polymorphisms (SNPs) by DNA chip analysis using Illumina Infinium Human-1 microarrays™ on 15 patients
 who underwent allogeneic HSCT with (N = 7) or without (N = 8) acute graft versus host disease (GvHD). Six SNPs (rs2504787, rs2504086, rs2504082, rs3004067, rs882559, and rs3004070)
 of DAAM2 were associated with acute GvHD prevalence, and the genotyping was extended to larger population (N = 228). Medical records were reviewed to see the correlation of these SNPs with the clinical outcomes of the patients. In
 rs2504082 and rs882559, treatment-related mortality was significantl...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5210165</comments>
            <pubDate>Fri, 09 Sep 2011 16:46:49 +0100</pubDate>
            <guid isPermaLink="false">5210165</guid>        </item>
        <item>
            <title>PET-negative pulmonary intravascular large B cell lymphoma diagnosed by a random transbronchial lung biopsy</title>
            <link>http://www.medworm.com/index.php?rid=5210164&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F6354h28453080n03%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorPages 1-2DOI 10.1007/s00277-011-1333-xAuthors
		Tomonori Nakazato, Department of Hematology, Yokohama Municipal Citizen’s Hospital, 56 Okazawa-cho, Hodogaya-ku, Yokohama, 240-8555 JapanYukinari Sanada, Department of Hematology, Yokohama Municipal Citizen’s Hospital, 56 Okazawa-cho, Hodogaya-ku, Yokohama, 240-8555 JapanAi Mihara, Department of Hematology, Yokohama Municipal Citizen’s Hospital, 56 Okazawa-cho, Hodogaya-ku, Yokohama, 240-8555 JapanChisako Ito, Department of Hematology, Yokohama Municipal Citizen’s Hospital, 56 Okazawa-cho, Hodogaya-ku, Yokohama, 240-8555 JapanYoshinobu Aisa, Department of Hematology, Yokohama Municipal Citizen’s Hospital, 56 Okazawa-cho, Hodogaya-ku, Yokohama, 240-8555 JapanNaoya Nakamura, D...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5210164</comments>
            <pubDate>Fri, 09 Sep 2011 16:46:49 +0100</pubDate>
            <guid isPermaLink="false">5210164</guid>        </item>
        <item>
            <title>TET2, ASXL1, IDH1, IDH2, and c-CBL genes in JAK2- and MPL-negative myeloproliferative neoplasms</title>
            <link>http://www.medworm.com/index.php?rid=5210166&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F1542qj12j986441u%2F</link>
            <description>In conclusion, TET2 and ASXL1 pathogenic mutations are found in 8% of MPN lacking JAK2 and MPL mutations, whereas IDH1, IDH2, and c-CBL mutations are not detected in this subset of patients.
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-9DOI 10.1007/s00277-011-1330-0Authors
		Luz Martínez-Avilés, Department of Pathology, Hospital del Mar, Barcelona, SpainCarlos Besses, Department of Clinical Hematology, Hospital del Mar, Passeig Marítim 25-29, 08003 Barcelona, SpainAlberto Álvarez-Larrán, Department of Clinical Hematology, Hospital del Mar, Passeig Marítim 25-29, 08003 Barcelona, SpainErica Torres, Department of Pathology, Hospital del Mar, Barcelona, SpainSergi Serrano, Department of Pathology, Hospital del Mar, Barcelona, SpainBeatriz Bellosillo, Department of P...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5210166</comments>
            <pubDate>Fri, 09 Sep 2011 05:49:56 +0100</pubDate>
            <guid isPermaLink="false">5210166</guid>        </item>
        <item>
            <title>Successful treatment of IgM-monoclonal gammopathy of undetermined significance associated with cryoglobulinemia and cold agglutinin disease with immunochemotherapy with rituximab, fludarabine, and cyclophosphamide</title>
            <link>http://www.medworm.com/index.php?rid=5210167&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn553312565763335%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorPages 1-3DOI 10.1007/s00277-011-1322-0Authors
		Joyeeta Bhattacharyya, Department of Hematology and Oncology, Research Institute for Radiation Biology and Medicine, Hiroshima University, 1-2-3 Kasumi, Minami-ku, Hiroshima, 734-8553 JapanKeichiro Mihara, Department of Hematology and Oncology, Research Institute for Radiation Biology and Medicine, Hiroshima University, 1-2-3 Kasumi, Minami-ku, Hiroshima, 734-8553 JapanYoshihiro Takihara, Department of Stem Cell Biology, Research Institute for Radiation Biology and Medicine, Hiroshima University, 1-2-3 Kasumi, Minami-ku, Hiroshima, 734-8553 JapanAkiro Kimura, Department of Hematology and Oncology, Research Institute for Radiation Biology and Medicine, Hiroshima University, 1-2-3 Kasum...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5210167</comments>
            <pubDate>Thu, 08 Sep 2011 06:09:28 +0100</pubDate>
            <guid isPermaLink="false">5210167</guid>        </item>
        <item>
            <title>Long-term results of thalidomide and dexamethasone (thal–dex) as therapy of first relapse in multiple myeloma</title>
            <link>http://www.medworm.com/index.php?rid=5210171&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl10vu46118307673%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Thal–dex (TD) is an effective therapy for advanced MM. We evaluated TD as salvage treatment of MM patients at first relapse.
 Thal was given at a daily dose of 100 or 200&amp;nbsp;mg until progression. Dex was administered 160&amp;nbsp;mg/month. One hundred patients
 were enrolled. First line therapy included ASCT (72%) and conventional CHT (28%). Fifty-nine percent received a fixed thal
 dose of 100&amp;nbsp;mg/day. The most frequent adverse events were constipation (42%), peripheral neuropathy (58%, 5% grade 3), bradycardia
 (20%), skin rash (11%), and VTE (7%). Discontinuation of thal due to adverse events was recorded in eight patients. On ITT,
 46% of patients achieved at least a PR. Median DOR was 28&amp;nbsp;months, median time to next therapy was 15.5&amp;nbsp;months. Median OS,
...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5210171</comments>
            <pubDate>Thu, 08 Sep 2011 06:09:27 +0100</pubDate>
            <guid isPermaLink="false">5210171</guid>        </item>
        <item>
            <title>Gene mutations in the Ras pathway and the prognostic implication in Korean patients with juvenile myelomonocytic leukemia</title>
            <link>http://www.medworm.com/index.php?rid=5210170&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fvh8718wu4r23r2k6%2F</link>
            <description>In this study, we investigated Ras pathway mutations
 and prognostic implication in Korean patients with JMML. A total of 22 Korean patients with JMML were recruited from two institutions
 (19 boys and three girls; median age, 17&amp;nbsp;months; range, 1–74&amp;nbsp;months). Hematologic and cytogenetic findings were reviewed.
 Mutation analyses involved PTPN11, KRAS, NRAS, and CBL genes by direct sequencing analyses (selected exons except in CBL). Survival analysis was performed by the Kaplan–Meier method. Cytogenetic and/or gene mutations were detected in 18 patients
 out of 22 (82%). Four patients (18%) had chromosomal abnormalities, with monosomy 7 being the most common. Seventeen (77%)
 had gene mutations. PTPN11 mutations were detected in 13 patients (59%). The patient heterozygous for c...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5210170</comments>
            <pubDate>Thu, 08 Sep 2011 06:09:27 +0100</pubDate>
            <guid isPermaLink="false">5210170</guid>        </item>
        <item>
            <title>New insights on pathophysiology, clinical manifestations, diagnosis, and treatment of sickle cell nephropathy</title>
            <link>http://www.medworm.com/index.php?rid=5210169&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fd43716877hrm449t%2F</link>
            <description>This article highlights the aspects of sickle cell nephropathy pathophysiology and clinical manifestations
 and describes the most recent advances in the diagnosis and treatment of this disorder.
 
 
	Content Type Journal ArticleCategory Review ArticlePages 1-9DOI 10.1007/s00277-011-1327-8Authors
		Geraldo Bezerra da Silva Junior, Post-Graduation Program in Medical Sciences, Department of Internal Medicine, Federal University of Ceará, Rua Vicente Linhares, 1198, CEP 60135-270 Fortaleza, Ceará, BrazilAlexandre Braga Libório, Medicine School, Health Sciences Center, University of Fortaleza, Fortaleza, Ceará, BrazilElizabeth De Francesco Daher, Post-Graduation Program in Medical Sciences, Department of Internal Medicine, Federal University of Ceará, Rua Vicente Linhares, 1198, CEP 60135...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5210169</comments>
            <pubDate>Thu, 08 Sep 2011 06:09:27 +0100</pubDate>
            <guid isPermaLink="false">5210169</guid>        </item>
        <item>
            <title>Targeted (not global) iron supplementation/fortification is the issue!</title>
            <link>http://www.medworm.com/index.php?rid=5210168&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fmn60235813714m36%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorPages 1-2DOI 10.1007/s00277-011-1336-7Authors
		Nils Milman, Department of Clinical Biochemistry, Næstved Hospital, Ringstedgade 61, 4700 Næstved, Denmark
	

	
		Journal Annals of HematologyOnline ISSN 1432-0584Print ISSN 0939-5555 (Source: Annals of Hematology)</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5210168</comments>
            <pubDate>Thu, 08 Sep 2011 06:09:27 +0100</pubDate>
            <guid isPermaLink="false">5210168</guid>        </item>
        <item>
            <title>Reduced intensity conditioning allogeneic hematopoietic stem cell transplant could be beneficial to angioimmunoblastic T-cell lymphoma patients with hemophagocytic lymphohistiocytosis</title>
            <link>http://www.medworm.com/index.php?rid=5210175&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F201781k777540312%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorPages 1-3DOI 10.1007/s00277-011-1328-7Authors
		Jui-Ting Yu, Division of Hematology/Oncology, Department of Medicine, Taichung Veterans General Hospital, 160, Section 3, Chungkang Road, Taichung, 407 TaiwanWen-Li Hwang, Division of Hematology/Oncology, Department of Medicine, Taichung Veterans General Hospital, 160, Section 3, Chungkang Road, Taichung, 407 TaiwanRen-Ching Wang, Department of Pathology, Taichung Veterans General Hospital, Taichung, TaiwanChieh-Lin Teng, Division of Hematology/Oncology, Department of Medicine, Taichung Veterans General Hospital, 160, Section 3, Chungkang Road, Taichung, 407 Taiwan
	

	
		Journal Annals of HematologyOnline ISSN 1432-0584Print ISSN 0939-5555 (Source: Annals of Hematology)</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5210175</comments>
            <pubDate>Mon, 05 Sep 2011 16:13:41 +0100</pubDate>
            <guid isPermaLink="false">5210175</guid>        </item>
        <item>
            <title>Spindle cell variant of multiple myeloma: immunophenotype and cytogenetics abnormalities</title>
            <link>http://www.medworm.com/index.php?rid=5210174&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ftm74242224456303%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorPages 1-2DOI 10.1007/s00277-011-1324-yAuthors
		Nahla M. Heikal, Department of Pathology, University of Utah and ARUP Reference Laboratory, Salt Lake City, UT, USAShashirekha Shetty, Department of Pathology, Cleveland Clinic Foundation, 9500 Euclid Ave. L23, Cleveland, OH 44195, USA
	

	
		Journal Annals of HematologyOnline ISSN 1432-0584Print ISSN 0939-5555 (Source: Annals of Hematology)</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5210174</comments>
            <pubDate>Mon, 05 Sep 2011 16:13:41 +0100</pubDate>
            <guid isPermaLink="false">5210174</guid>        </item>
        <item>
            <title>Circulating IL-17 levels during the peri-transplant period as a predictor for early leukemia relapse after myeloablative allogeneic stem cell transplantation</title>
            <link>http://www.medworm.com/index.php?rid=5210173&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F367788n45807j7v2%2F</link>
            <description>This study is the first one demonstrating the early
 change in sIL-17 during the peri-transplant period and the association with early relapse in humans.
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-10DOI 10.1007/s00277-011-1318-9Authors
		Byung-Sik Cho, Department of Hematology, Catholic Blood and Marrow Transplantation Center, Seoul St. Mary’s Hospital, College of Medicine, The Catholic University of Korea, #505 Banpo-dong, Seocho-gu, Seoul 137-701, South KoreaJi-Young Lim, Department of Hematology, Catholic Blood and Marrow Transplantation Center, Seoul St. Mary’s Hospital, College of Medicine, The Catholic University of Korea, #505 Banpo-dong, Seocho-gu, Seoul 137-701, South KoreaSeung-Ah Yahng, Department of Hematology, Catholic Blood and Marrow Transplantatio...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5210173</comments>
            <pubDate>Mon, 05 Sep 2011 16:13:41 +0100</pubDate>
            <guid isPermaLink="false">5210173</guid>        </item>
        <item>
            <title>Autoimmune myelofibrosis as the first manifestation of human immunodeficiency virus infection in an infant</title>
            <link>http://www.medworm.com/index.php?rid=5210172&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb6868j1520kk7765%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorPages 1-2DOI 10.1007/s00277-011-1329-6Authors
		Anselm Chi-wai Lee, Children’s Haematology and Cancer Centre, Mount Elizabeth Hospital, Level 4, 3 Mount Elizabeth, Singapore, 228510 SingaporeChee Meng Fong, Parkway Laboratory Services, Mount Elizabeth Hospital, Singapore, Singapore
	

	
		Journal Annals of HematologyOnline ISSN 1432-0584Print ISSN 0939-5555 (Source: Annals of Hematology)</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5210172</comments>
            <pubDate>Mon, 05 Sep 2011 16:13:41 +0100</pubDate>
            <guid isPermaLink="false">5210172</guid>        </item>
        <item>
            <title>Efficacy and safety of micafungin as an empirical antifungal therapy for suspected fungal infection in neutropenic patients with hematological disorders</title>
            <link>http://www.medworm.com/index.php?rid=5210176&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F14867j818240834p%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;This prospective multicenter study was performed to clarify the efficacy and safety of micafungin (MCFG) as an empirical antifungal
 therapy for suspected fungal infection in patients with hematological disorders and neutropenia. Three hundred and eighty-eight
 patients were enrolled; 151 patients with possible fungal infection diagnosed by radiological imaging or serological testing
 and 237 patients with refractory fever were included in this study. The mean dose and duration of treatment with MCFG were
 154.6&amp;nbsp;mg/day and 14.0&amp;nbsp;days, respectively. The clinical response rate for patients with possible fungal infection and refractory
 fever was 60.1% and 65.3%, respectively. Even in persistent neutropenic patients with a neutrophil count of &amp;lt;500/μL throughou...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5210176</comments>
            <pubDate>Mon, 05 Sep 2011 16:13:39 +0100</pubDate>
            <guid isPermaLink="false">5210176</guid>        </item>
        <item>
            <title>Tcf-1 gene silence suppresses downstream gene expression in CD4+ T cells from bone marrow of aplastic anemia patients</title>
            <link>http://www.medworm.com/index.php?rid=5184964&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb124752404t76l15%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;CD4+ T cells play a crucial role in the pathogenesis of acquired aplastic anemia (AA). Tcf-1 gene regulates T cell development
 and function, and it is significantly upregulated in the bone marrow CD4+ T cells from patients with acquired AA. To explore the role of Tcf-1 in the pathogenesis of AA, we knocked down Tcf-1 gene
 in CD4+ T cells of AA patients and studied the effects of Tcf-1 silencing on its downstream gene expression. Upon transfection of
 psiRNA into marrow CD4+ T cells from bone marrow of aplastic anemia patients, the expression of Tcf-1 was significantly knocked down; consequently,
 expressions of c-Myc and CD44 were also significantly reduced. Our results suggest that Tcf-1 may contribute to pathogenesis
 of AA by regulating downstream gene expression s...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5184964</comments>
            <pubDate>Wed, 31 Aug 2011 15:53:14 +0100</pubDate>
            <guid isPermaLink="false">5184964</guid>        </item>
        <item>
            <title>3,4-Diarylmaleimides—a novel class of kinase inhibitors—effectively induce apoptosis in FLT3-ITD-dependent cells</title>
            <link>http://www.medworm.com/index.php?rid=5184963&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fkt2511k038kh0q7j%2F</link>
            <description>In conclusion, this novel group of compounds shows differential inhibition patterns with regard to FLT3 kinase and displays
 a promising profile for further clinical development. Currently, experiments evaluating toxicity in murine models and unraveling
 the exact binding mechanism are under way to facilitate a potential clinical application.
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-14DOI 10.1007/s00277-011-1311-3Authors
		Florian H. Heidel, Department of Hematology and Oncology, Medical Center, Otto-von-Guericke University, Leipzigerstr. 44, 39120 Magdeburg, GermanyThomas S. Mack, Department of Hematology and Oncology, Medical Center, Otto-von-Guericke University, Leipzigerstr. 44, 39120 Magdeburg, GermanyElena Razumovskaya, Experimental Clinical Chemistry, Wallen...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5184963</comments>
            <pubDate>Wed, 31 Aug 2011 15:53:14 +0100</pubDate>
            <guid isPermaLink="false">5184963</guid>        </item>
        <item>
            <title>An imatinib-treated FIL1P1-PDGFRα chronic eosinophilic leukemia transforming to erythroid blast crisis: a case report</title>
            <link>http://www.medworm.com/index.php?rid=5184965&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ft2063736ww57x518%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorPages 1-3DOI 10.1007/s00277-011-1312-2Authors
		Xenofon Papanikolaou, “Henry Dunant” General Hospital, Athens, GreeceMaria Kotsopoulou, “Metaxa” Specialized Anticancer Hospital of Piraeus, Piraeus, GreeceI. Diana Triantafillopoulou, “Metaxa” Specialized Anticancer Hospital of Piraeus, Piraeus, GreeceAthanasia Zoi, Biomedical Research Institute of Academy of Athens, Athens, GreeceVasilis Chatziantoniou, “Metaxa” Specialized Anticancer Hospital of Piraeus, Piraeus, GreeceDimitrios Maltezas, “Metaxa” Specialized Anticancer Hospital of Piraeus, Piraeus, GreeceChrysanthi Mitsouli-Mentzikof, “Metaxa” Specialized Anticancer Hospital of Piraeus, Piraeus, Greece
	

	
		Journal Annals of HematologyOnline ISSN 1432-058...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5184965</comments>
            <pubDate>Wed, 31 Aug 2011 15:53:12 +0100</pubDate>
            <guid isPermaLink="false">5184965</guid>        </item>
        <item>
            <title>Quantification of plasma Epstein–Barr virus DNA for assessing treatment response in a patient with plasmablastic lymphoma</title>
            <link>http://www.medworm.com/index.php?rid=5184966&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F257v2v5606854625%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorPages 1-3DOI 10.1007/s00277-011-1313-1Authors
		Man Fai Law, Department of Medicine, Tuen Mun Hospital, Hong Kong, ChinaWai Lun Poon, Department of Radiology, Tuen Mun Hospital, Hong Kong, ChinaKwan Shun Ng, Department of Pathology, Tuen Mun Hospital, Hong Kong, ChinaHay Nun Chan, Department of Medicine, Tuen Mun Hospital, Hong Kong, ChinaHo Kei Lai, Department of Medicine, Tuen Mun Hospital, Hong Kong, ChinaChun Yin Ha, Department of Medicine, Tuen Mun Hospital, Hong Kong, ChinaCelia Ng, Department of Medicine, Tuen Mun Hospital, Hong Kong, ChinaYiu Ming Yeung, Department of Medicine, Tuen Mun Hospital, Hong Kong, ChinaSze Fai Yip, Department of Medicine, Tuen Mun Hospital, Hong Kong, China
	

	
		Journal Annals of HematologyOnlin...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5184966</comments>
            <pubDate>Wed, 31 Aug 2011 15:53:11 +0100</pubDate>
            <guid isPermaLink="false">5184966</guid>        </item>
        <item>
            <title>Treatment for orbital diffuse large B-cell lymphoma in an elderly patient by autologous cytokine-induced killer cells</title>
            <link>http://www.medworm.com/index.php?rid=5163474&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F43rh22k13tp87155%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorPages 1-2DOI 10.1007/s00277-011-1301-5Authors
		Su-Xia Li, Department of Geriatric Hematology, Chinese People’s Liberation Army General Hospital, Beijing, 100853 ChinaHong-Li Zhu, Department of Geriatric Hematology, Chinese People’s Liberation Army General Hospital, Beijing, 100853 ChinaBo Guo, Department of Geriatric Hematology, Chinese People’s Liberation Army General Hospital, Beijing, 100853 ChinaXue-Chun Lu, Department of Geriatric Hematology, Chinese People’s Liberation Army General Hospital, Beijing, 100853 ChinaBo Yang, Department of Geriatric Hematology, Chinese People’s Liberation Army General Hospital, Beijing, 100853 ChinaYang Liu, Department of Geriatric Hematology, Chinese People’s Liberation Army General ...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5163474</comments>
            <pubDate>Fri, 19 Aug 2011 05:50:57 +0100</pubDate>
            <guid isPermaLink="false">5163474</guid>        </item>
        <item>
            <title>Replacement of conventional doxorubicin by pegylated liposomal doxorubicin is a safe and effective alternative in the treatment of non-Hodgkin's lymphoma patients with cardiac risk factors</title>
            <link>http://www.medworm.com/index.php?rid=5163475&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fc4mk66g12ptq48p8%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Anthracyclines are a major component in the therapy of non-Hodgkin's lymphoma. However, due to their cardiac toxicity potential,
 curative and palliative treatment is often limited in patients with preexisting cardiac dysfunction. Liposomal doxorubicin
 formulations have been described to be less cardiotoxic than conventional doxorubicin. In the current study, we analyzed the
 efficacy and toxicity of pegylated liposomal doxorubicin (PLD) as constituent of the cyclophosphamide, doxorubicin, vincristine,
 and prednisone (CHOP) regimen replacing conventional doxorubicin in 21 patients with impaired cardiac left ventricular ejection
 fraction or preexisting cardiac risk factors and established diagnosis of diffuse large B cell lymphoma (n = 15), mantle cell lymphoma (n...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5163475</comments>
            <pubDate>Thu, 18 Aug 2011 06:02:36 +0100</pubDate>
            <guid isPermaLink="false">5163475</guid>        </item>
        <item>
            <title>Another Hb with inclusion bodies β-thalassemia, owing to Hb Durham-N.C. [β114(G16) Leu &gt; Pro]. First case described in Hispanic populations</title>
            <link>http://www.medworm.com/index.php?rid=5163476&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F84qtu87q8vng16jr%2F</link>
            <description>Another Hb with inclusion bodies β-thalassemia, owing to Hb Durham-N.C. [β114(G16) Leu &gt; Pro]. First case described in Hispanic populations
	Content Type Journal ArticleCategory Letter to the EditorPages 1-4DOI 10.1007/s00277-011-1310-4Authors
		Paloma Ropero, Servicio de Hematología, Hospital Clínico San Carlos, C/Profesor Martín Lagos s/n, 28040 Madrid, SpainRaúl Córdoba, Servicio de Hematología, Hospital Infanta Sofía, Madrid, SpainMarta Morado, Servicio de Hematología, Hospital Universitario La Paz, Madrid, SpainFernando Ataulfo González, Servicio de Hematología, Hospital Clínico San Carlos, C/Profesor Martín Lagos s/n, 28040 Madrid, SpainAna Villegas, Servicio de Hematología, Hospital Clínico San Carlos, C/Profesor Martín Lagos s/n, 28040 Madrid, SpainErythropathology...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5163476</comments>
            <pubDate>Tue, 16 Aug 2011 06:18:50 +0100</pubDate>
            <guid isPermaLink="false">5163476</guid>        </item>
        <item>
            <title>Nutritional status independently affects quality of life of patients with systemic immunoglobulin light-chain (AL) amyloidosis</title>
            <link>http://www.medworm.com/index.php?rid=5120506&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fnl5v6706k50g8127%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Nutritional status is an independent prognostic factor in immunoglobulin light-chain amyloidosis (AL), but its influence on
 quality of life (QoL) is unknown. The aim of this cross-sectional study was to investigate the association between nutritional
 status and QoL in AL patients at diagnosis. One hundred and fifty consecutive patients with biopsy-proven AL were assessed
 for nutritional status by anthropometry [body mass index, unintentional weight loss (WL) in the previous 6&amp;nbsp;months and mid-arm
 muscle circumference (MAMC)], biochemistry (serum prealbumin), and semiquantitative food intake at referral. QoL was assessed
 by the Medical Outcomes Study 36-item Short Form General Health Survey. The composite physical component summary (PCS) and
 the mental component...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5120506</comments>
            <pubDate>Mon, 08 Aug 2011 19:53:16 +0100</pubDate>
            <guid isPermaLink="false">5120506</guid>        </item>
        <item>
            <title>Retrospective analysis of primary gastric diffuse large B cell lymphoma in the rituximab era: a multicenter study of 95 patients in Japan</title>
            <link>http://www.medworm.com/index.php?rid=5110575&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F420j331154265n80%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Primary gastric diffuse large B cell lymphoma (PG-DLBCL) is common subtype of extranodal non-Hodgkin lymphoma. The optimal
 treatment strategy for PG-DLBCL in the rituximab era still remains unknown. To evaluate clinical outcomes of PG-DLBCL in the
 rituximab era, we conducted a retrospective, multicenter analysis of 95 patients with PG-DLBCL. In 58 patients with localized
 disease, 3-year progression-free survival (PFS) and overall survival (OS) were 91% and 91% for patients with six cycles of
 rituximab plus CHOP (R-CHOP) and 92% and 95% for patients with three to four cycles of R-CHOP plus radiotherapy (Log-rank
 test, P = 0.595 and P = 0.278, respectively). In 37 patients with advanced disease, 3-year PFS and 3-year OS were 43% and 64% for patients with
 R-C...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5110575</comments>
            <pubDate>Sat, 06 Aug 2011 05:45:12 +0100</pubDate>
            <guid isPermaLink="false">5110575</guid>        </item>
        <item>
            <title>In vitro vessel-forming capacity of endothelial progenitor cells in high glucose conditions</title>
            <link>http://www.medworm.com/index.php?rid=5110576&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb238h05818q76123%2F</link>
            <description>In this study, we established a quantitative methodology to assess EPC function by using an in vitro 5-(6)-carboxyfluorescein
 diacetate succinimidyl ester-labeling vessel formation assay. The EPCs were cultured in three different glucose concentrations
 (100, 189.5, and 295.5&amp;nbsp;mg/dl of d-glucose) representing normal control and diabetes with either good or poor glycemic control, respectively. We found that
 the in vitro vessel-forming capacity was impaired in EPCs cultured in high glucose concentrations compared to normal control
 (43.4 ± 0.8% and 34.7 ± 0.7% vs. 50.8 ± 2.1%). We further studied expression of various genes involved in vessel formation.
 There was a lower level of angiopoietin 1 gene expression in EPCs cultured in high glucose concentrations. The additio...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5110576</comments>
            <pubDate>Sat, 06 Aug 2011 05:45:11 +0100</pubDate>
            <guid isPermaLink="false">5110576</guid>        </item>
        <item>
            <title>Severe CMV reactivation and gastritis during treatment of follicular lymphoma with bendamustine</title>
            <link>http://www.medworm.com/index.php?rid=5098730&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F8333w5tv92k5w286%2F</link>
            <description>Content Type Journal ArticlePages 1-2DOI 10.1007/s00277-011-1307-zAuthors
		Seah H. Lim, Texas Oncology-Amarillo Cancer Center, Amarillo, TX, USASrinivas Pathapati, Texas Oncology-Amarillo Cancer Center, Amarillo, TX, USAJames Langevin, Texas Oncology-Amarillo Cancer Center, Amarillo, TX, USAAndrew Hoot, Texas Oncology-Amarillo Cancer Center, Amarillo, TX, USA
	

	
		Journal Annals of HematologyOnline ISSN 1432-0584Print ISSN 0939-5555 (Source: Annals of Hematology)</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5098730</comments>
            <pubDate>Tue, 02 Aug 2011 15:52:11 +0100</pubDate>
            <guid isPermaLink="false">5098730</guid>        </item>
        <item>
            <title>Lymphopenia following the completion of first-line therapy predicts early relapse in patients with diffuse large B cell lymphoma</title>
            <link>http://www.medworm.com/index.php?rid=5098731&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fpr01837861mr6568%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Early relapse is a parameter that affects clinical outcomes in relapsed diffuse large B cell lymphoma (DLBCL). The prognostic
 value of lymphopenia following the completion of first-line therapy and the relationship between lymphopenia and early relapse
 are unknown. Therefore, we studied the role of absolute lymphocyte count (ALC) on early relapse. We retrospectively analyzed
 de novo DLBCL patients who were treated with rituximab-containing treatment between 2003 and 2010. The median age at the time
 of diagnosis of 59 DLBCL patients was 71&amp;nbsp;years. We identified no association between ALC at diagnosis and ALC following the
 completion of first-line therapy. Among all patients analyzed, 13 (22%) patients were confirmed to exhibit early relapse.
 Low ALC following t...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5098731</comments>
            <pubDate>Tue, 02 Aug 2011 15:52:08 +0100</pubDate>
            <guid isPermaLink="false">5098731</guid>        </item>
        <item>
            <title>Circulating CD133+VEGFR2+ and CD34+VEGFR2+ cells and arterial function in patients with beta-thalassaemia major</title>
            <link>http://www.medworm.com/index.php?rid=5098732&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F808872172p64246x%2F</link>
            <description>In conclusion, arterial dysfunction
 found in patients with beta-thalassaemia major before and after HSCT may be related to impaired proliferation of CD133+VEGFR2+ and CD34+VEGFR2+ cells.
 
 
	Content Type Journal ArticlePages 1-8DOI 10.1007/s00277-011-1302-4Authors
		Yiu-fai Cheung, Division of Paediatric Cardiology, Department of Paediatrics and Adolescent Medicine, Queen Mary Hospital, The University of Hong Kong, 102, Pokfulam Road, Hong Kong, ChinaShing Chan, Division of Paediatric Cardiology, Department of Paediatrics and Adolescent Medicine, Queen Mary Hospital, The University of Hong Kong, 102, Pokfulam Road, Hong Kong, ChinaMo Yang, Division of Paediatric Cardiology, Department of Paediatrics and Adolescent Medicine, Queen Mary Hospital, The University of Hong Kong, 102, Pokfulam ...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5098732</comments>
            <pubDate>Tue, 02 Aug 2011 06:17:12 +0100</pubDate>
            <guid isPermaLink="false">5098732</guid>        </item>
        <item>
            <title>CD14−/CD34+ is the founding population of umbilical cord blood-derived endothelial progenitor cells and angiogenin1 is an important factor promoting the colony formation</title>
            <link>http://www.medworm.com/index.php?rid=5098733&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp73vl34243l522j3%2F</link>
            <description>In this study, we explored the
 origin of UCB-derived EPCs by culturing CD14+ or CD14− subpopulation separately and co-culturing these two subpopulations
 either with or without transwells. We found no colony formation with CD14+ or CD14− subpopulation alone, but there were EPC
 colonies observed in direct co-cultures of both subpopulations. Transwell culture system was used to further study the effect
 of cytokines on EPC colony formation. We observed the presence of EPC colonies derived from CD14− subpopulation in the presence
 of CD14+ subpopulation in the upper compartment whereas there was no colony generated from CD14+ subpopulation with CD14−
 subpopulation in the upper compartment. Therefore, CD14− subpopulation is likely to be the origin of EPCs and EPC colony derivation...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5098733</comments>
            <pubDate>Tue, 02 Aug 2011 06:17:11 +0100</pubDate>
            <guid isPermaLink="false">5098733</guid>        </item>
        <item>
            <title>Diagnostic and therapeutic challenges of severe Rh e-specific IgA-mediated autoimmune hemolytic anemia</title>
            <link>http://www.medworm.com/index.php?rid=5089150&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fqp2717m347314133%2F</link>
            <description>Content Type Journal ArticlePages 1-2DOI 10.1007/s00277-011-1304-2Authors
		Leonie A. Boven, Department of Clinical Chemistry, Meander Medical Centre, Utrechtseweg 160, 3818 ES Amersfoort, The NetherlandsAmy de Haar-Holleman, Department of Hematology, Meander Medical Centre, Amersfoort, The NetherlandsClaudia C. Folman, Sanquin Diagnostics, Amsterdam, The NetherlandsRob J. Kraaijenhagen, Department of Clinical Chemistry, Meander Medical Centre, Utrechtseweg 160, 3818 ES Amersfoort, The NetherlandsRob Fijnheer, Department of Hematology, Meander Medical Centre, Amersfoort, The Netherlands
	

	
		Journal Annals of HematologyOnline ISSN 1432-0584Print ISSN 0939-5555 (Source: Annals of Hematology)</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5089150</comments>
            <pubDate>Fri, 29 Jul 2011 16:05:56 +0100</pubDate>
            <guid isPermaLink="false">5089150</guid>        </item>
        <item>
            <title>Allogeneic bone marrow transplantation compared to peripheral blood stem cell transplantation for the treatment of hematologic malignancies: a meta-analysis based on time-to-event data from randomized controlled trials</title>
            <link>http://www.medworm.com/index.php?rid=5080862&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F6g61w02555v55252%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Controversy remains regarding the transplant outcomes of human leukocyte antigen-identical related bone marrow transplantation
 (BMT) and peripheral blood stem cell transplantation (PBSCT) for the treatment of patients with hematological malignancies.
 To provide an estimate of the effect of BMT and PBSCT on clinical outcomes in patients with hematological malignancies, we
 conducted a meta-analysis based on time-to-event data from 17 randomized controlled trials. PubMed, EMBASE, and Cochrane Central
 Register of Controlled Trials (CENTRAL), from 1972 through July 2010, and conference proceedings through July 2009 and reference
 lists, without any language restriction, of randomized trials that compared the transplant outcomes after BMT and PBSCT in
 patients with hemat...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5080862</comments>
            <pubDate>Tue, 26 Jul 2011 05:51:26 +0100</pubDate>
            <guid isPermaLink="false">5080862</guid>        </item>
        <item>
            <title>Prevalence and progression of monoclonal gammopathy of undetermined significance and light-chain MGUS in Germany</title>
            <link>http://www.medworm.com/index.php?rid=5080863&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fd616822m4n16625m%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;We determined the prevalence and progression rate of monoclonal gammopathy of undetermined significance (MGUS) and light-chain
 MGUS (LCMGUS) in Germany utilizing the biobank of the population-based Heinz Nixdorf Recall Study. The Heinz Nixdorf Recall
 Study comprises 4,814 men and women aged 45–75&amp;nbsp;years. To detect monoclonal proteins, standard serum electrophoresis was combined
 with parallel screening immunofixation using pentavalent antisera. Additionally, free light chains (FLC) were measured in
 all samples. Definition of MGUS included M-protein concentration, laboratory results, and disease history. LCMGUS was defined
 as abnormal FLC ratio, increase in FLC causing the abnormal ratio, and lack of intact immunoglobulin. One hundred sixty-five
 MGUS cases wer...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5080863</comments>
            <pubDate>Tue, 26 Jul 2011 05:51:24 +0100</pubDate>
            <guid isPermaLink="false">5080863</guid>        </item>
        <item>
            <title>Sequential vincristine, adriamycin, dexamethasone (VAD) followed by bortezomib, thalidomide, dexamethasone (VTD) as induction, followed by high-dose therapy with autologous stem cell transplant and consolidation therapy with bortezomib for newly diagnosed multiple myeloma: results of a phase II trial</title>
            <link>http://www.medworm.com/index.php?rid=5080864&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F54206p754574t658%2F</link>
            <description>In conclusion, sequential VAD and VTD induction
 therapy in patients with newly diagnosed multiple myeloma was active with manageable toxicity and excellent stem cell yields.
 The incorporation of bortezomib as a consolidation therapy improved the clinical outcome with the expense of rather frequent
 development of peripheral neuropathy.
 
 
	Content Type Journal ArticlePages 1-8DOI 10.1007/s00277-011-1298-9Authors
		Hye Jin Kim, The Armed Forces Capital Hospital, Seoul, South KoreaSung-Soo Yoon, Clinical Research Institute, Seoul National University College of Medicine, Seoul, South KoreaDong Soon Lee, Clinical Research Institute, Seoul National University College of Medicine, Seoul, South KoreaSang Kyun Sohn, Kyungbook National University Hospital, Daegu, South KoreaHyeon Seok Eom, Natio...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5080864</comments>
            <pubDate>Tue, 26 Jul 2011 05:51:23 +0100</pubDate>
            <guid isPermaLink="false">5080864</guid>        </item>
        <item>
            <title>Clinical features and outcomes of Hodgkin’s lymphoma in Korea: Consortium for Improving Survival of Lymphoma (CISL)</title>
            <link>http://www.medworm.com/index.php?rid=5070560&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fmr51l71055406n81%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Ethnic and regional differences in the epidemiology and pathological aspects of Hodgkin’s lymphoma (HL) between Western and
 Asian patients may be associated with differences in clinical features and prognosis. We retrospectively analyzed the clinical
 and histopathological characteristics, therapeutic outcomes, and prognostic factors of 539 HL patients treated at 16 centers
 in Korea. We found that the incidence of histological subtypes of HL in Korea was similar to that in Western and other Asian
 countries. However, the incidence peaked between 16 and 30&amp;nbsp;years of age, unlike the bimodal age distribution seen in Western
 countries. In patients with stage I–IIA non-bulky disease, the complete response (CR) rate was similar between combined modality
 therapy an...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5070560</comments>
            <pubDate>Mon, 25 Jul 2011 15:47:54 +0100</pubDate>
            <guid isPermaLink="false">5070560</guid>        </item>
        <item>
            <title>Increased number of B-cells in the red pulp of the spleen in ITP</title>
            <link>http://www.medworm.com/index.php?rid=5064322&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F832852gpk438v615%2F</link>
            <description>In conclusion, B-cells are increased in the red pulp of the spleen
 and together with cytotoxic T-cells, helper T-cells and macrophages line the sinusoids enabling the immunological attack on
 platelets in ITP.
 
 
	Content Type Journal ArticlePages 1-7DOI 10.1007/s00277-011-1292-2Authors
		Bob Olsson, Department of Psychiatry and Neurochemistry, University of Gothenburg, Mölndal, SwedenBörje Ridell, Department of Pathology the Sahlgrenska Academy, University of Gothenburg, Gothenburg, SwedenMargareta Jernås, Department of Internal Medicine the Sahlgrenska Academy, University of Gothenburg, Gothenburg, SwedenHans Wadenvik, Department of Internal Medicine the Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden
	

	
		Journal Annals of HematologyOnline ISSN 1432-0584Print IS...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5064322</comments>
            <pubDate>Fri, 22 Jul 2011 17:06:27 +0100</pubDate>
            <guid isPermaLink="false">5064322</guid>        </item>
        <item>
            <title>Chronic myeloproliferative disorder with ETV6-PDGFRβ fusion gene</title>
            <link>http://www.medworm.com/index.php?rid=5064323&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fcu840g6v1kl8471r%2F</link>
            <description>Content Type Journal ArticlePages 1-2DOI 10.1007/s00277-011-1296-yAuthors
		Eswar Tipirneni, St.Vincent Hospital, Internal Medicine, Worcester, MA, USAAmanpreet Buttar, Department of Hematology/Oncology, UMASS Memorial Medical Center, Worcester, MA, USADoreen Brettler, Department of Hematology, UMASS Memorial Medical Center, Worcester, MA, USAPatricia Miron, Department of Cytogenetics, UMASS Memorial Medical Center, Worcester, MA, USAVenu Bathini, Department of Hematology/Oncology, UMASS Memorial Medical Center, Worcester, MA, USA
	

	
		Journal Annals of HematologyOnline ISSN 1432-0584Print ISSN 0939-5555 (Source: Annals of Hematology)</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5064323</comments>
            <pubDate>Thu, 21 Jul 2011 18:15:35 +0100</pubDate>
            <guid isPermaLink="false">5064323</guid>        </item>
        <item>
            <title>Are int22h-mediated deletions a common cause of hemophilia?</title>
            <link>http://www.medworm.com/index.php?rid=5064324&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk050gjv2t0h8870w%2F</link>
            <description>Content Type Journal ArticlePages 1-4DOI 10.1007/s00277-011-1295-zAuthors
		Miguel Martín Abelleyro, Departamento de Genética, Instituto de Investigaciones Hematológicas, Academia Nacional de Medicina de Buenos Aires, Pacheco de Melo 3081, Buenos Aires, 1425 ArgentinaLiliana Carmen Rossetti, Departamento de Genética, Instituto de Investigaciones Hematológicas, Academia Nacional de Medicina de Buenos Aires, Pacheco de Melo 3081, Buenos Aires, 1425 ArgentinaClaudia Pamela Radic, Departamento de Genética, Instituto de Investigaciones Hematológicas, Academia Nacional de Medicina de Buenos Aires, Pacheco de Melo 3081, Buenos Aires, 1425 ArgentinaMiguel Candela, Departamento de Hemoterapia y Hemofilia, Instituto de Investigaciones Hematológicas, Academia Nacional de Medicina de Buenos ...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5064324</comments>
            <pubDate>Tue, 19 Jul 2011 23:38:13 +0100</pubDate>
            <guid isPermaLink="false">5064324</guid>        </item>
        <item>
            <title>Levamisole—adulterated in cocaine causing agranulocytosis, vasculopathy, and acquired protein S deficiency</title>
            <link>http://www.medworm.com/index.php?rid=5064325&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb2520555671327x4%2F</link>
            <description>Content Type Journal ArticlePages 1-2DOI 10.1007/s00277-011-1294-0Authors
		Irene Dy, Department of Hematology and Oncology, St. Luke’s Roosevelt Hospital, 1000 Tenth Avenue 11G, New York, NY, USAVenkata Pokuri, Department of Internal Medicine, St. Luke’s Roosevelt Hospital, 1000 Tenth Avenue 11G, New York, NY, USAJohn Olichney, Department of Hematology and Oncology, St. Luke’s Roosevelt Hospital, 1000 Tenth Avenue 11G, New York, NY, USAPeter Wiernik, Department of Hematology and Oncology, St. Luke’s Roosevelt Hospital, 1000 Tenth Avenue 11G, New York, NY, USA
	

	
		Journal Annals of HematologyOnline ISSN 1432-0584Print ISSN 0939-5555 (Source: Annals of Hematology)</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5064325</comments>
            <pubDate>Tue, 19 Jul 2011 23:38:12 +0100</pubDate>
            <guid isPermaLink="false">5064325</guid>        </item>
        <item>
            <title>Brain positron emission tomography in splenectomized adults with β-thalassemia intermedia: uncovering yet another covert abnormality</title>
            <link>http://www.medworm.com/index.php?rid=5031317&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl3568145q4q4h231%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Covert brain infarction is an emerging concern in patients with β-thalassemia intermedia (TI). We have recently observed a
 high prevalence (60%) of silent brain infarction on brain magnetic resonance imaging (MRI) in 30 splenectomized adults with
 TI. In this work, we further evaluate cerebral involvement in the same 30 patients using fluorodeoxyglucose positron emission
 tomography–computed tomography (PET-CT) scanning. The median age was 32&amp;nbsp;years (range, 18–54&amp;nbsp;years) with a male to female ratio
 of 13:17. Nineteen patients (63.3%) had evidence of decreased neuronal function on PET-CT. Involvement was mostly left sided,
 multiple, and most commonly in the temporal and parietal lobes. Elevated liver iron concentration, beyond 15&amp;nbsp;mg Fe/g dry weight,
...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5031317</comments>
            <pubDate>Wed, 13 Jul 2011 06:17:34 +0100</pubDate>
            <guid isPermaLink="false">5031317</guid>        </item>
        <item>
            <title>Morphology, cytogenetics, and survival in myelodysplasia with del(20q) or ider(20q): a multicenter study</title>
            <link>http://www.medworm.com/index.php?rid=5021755&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ft3224373p4x38746%2F</link>
            <description>This study performed on the largest cohort of MDS patients with ider(20q)
 is the first that identifies specific morphological features (hypogranulated and vacuolized neutrophils and neutrophil erythrophagocytosis)
 allowing the identification of this cytogenetic abnormality with high sensitivity (70%) and specificity (85.7%). Suspected
 ider(20q) by morphology should therefore support targeted FISH tests in case of non informative karyotype. This combined approach
 will allow a better estimation of the prevalence of this underdiagnozed entity. The overall survival and progression-free
 survival did not statistically differ in both groups. However, hypogranulated and vacuolized neutrophils were significantly
 associated with survival.
 
 
	Content Type Journal ArticlePages 1-11DOI 10.1007/...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5021755</comments>
            <pubDate>Sat, 09 Jul 2011 06:16:55 +0100</pubDate>
            <guid isPermaLink="false">5021755</guid>        </item>
        <item>
            <title>Age-dependent frequencies of NPM1 mutations and FLT3-ITD in patients with normal karyotype AML (NK-AML)</title>
            <link>http://www.medworm.com/index.php?rid=5021756&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fa6753166t397lq64%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Prognosis of AML in elderly patients is poor due to adverse patient characteristics and comorbidities. In addition, disease-associated
 parameters reveal differences between older and younger patients with AML. Survival in normal karyotype AML (NK-AML) is influenced
 by different clinical and molecular markers. The aim of this work was to investigate the frequencies of molecular markers
 in patients with NK-AML with a focus on NPM1 mutations and FLT3-ITD in different age groups. In the present study, we analyzed the frequencies of mutations of NPM1 and FLT3-ITD in a cohort of 1,321 adult patients and 148 children with AML treated within the AMLCG99, the AML98, and AML04 trials
 and their distribution in different age groups. Additionally, the frequencies of mutations in...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5021756</comments>
            <pubDate>Sat, 09 Jul 2011 06:16:54 +0100</pubDate>
            <guid isPermaLink="false">5021756</guid>        </item>
        <item>
            <title>Liver failure as the only clinical manifestation of multiple myeloma</title>
            <link>http://www.medworm.com/index.php?rid=5010599&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl864959t8j3jl178%2F</link>
            <description>Content Type Journal ArticlePages 1-3DOI 10.1007/s00277-011-1284-2Authors
		David Coffey, Department of Medicine, University of Colorado Denver, 12631 East 17th Avenue, #B177, P.O. Box 6511, Aurora, CO 80045, USABrandon Fain, School of Medicine, University of Colorado Denver, Aurora, CO, USAChristopher Thompson, Division of Hematology-Oncology, University of Colorado Denver, Aurora, CO, USAEdward D. Chan, Department of Medicine, University of Colorado Denver, 12631 East 17th Avenue, #B177, P.O. Box 6511, Aurora, CO 80045, USASamia Nawaz, Department of Pathology, University of Colorado Denver and Veteran Affairs Medical Center, Aurora, CO, USA
	

	
		Journal Annals of HematologyOnline ISSN 1432-0584Print ISSN 0939-5555 (Source: Annals of Hematology)</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5010599</comments>
            <pubDate>Wed, 06 Jul 2011 05:55:40 +0100</pubDate>
            <guid isPermaLink="false">5010599</guid>        </item>
        <item>
            <title>Functional analysis and gene expression profile of umbilical cord blood regulatory T cells</title>
            <link>http://www.medworm.com/index.php?rid=5010600&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F35p6l445qg175054%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The aim of the study was to analyze and compare the functional properties and the gene expression profile of regulatory T
 cells (Tregs) isolated from cord blood (CB) units (n = 23) and from the peripheral blood (PB) of adult normal donors (n = 13). Tregs were purified from mononuclear cells and expanded for 6&amp;nbsp;days with anti-CD3, anti-CD28, and IL-2. CB and PB Tregs
 presented similar immunophenotypic features. However, Tregs isolated from CB presented a much higher expansion capacity; this
 was confirmed by the genomic characterization that showed in CB-derived Tregs significant enrichments of genes involved in
 cell proliferation, chromatin modification, and regulation of gene expression. All samples were positive for the FoxP3 gene
 and protein after exp...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5010600</comments>
            <pubDate>Wed, 06 Jul 2011 05:55:39 +0100</pubDate>
            <guid isPermaLink="false">5010600</guid>        </item>
        <item>
            <title>Transcriptomic rationale for the synergy observed with dasatinib + bortezomib + dexamethasone in multiple myeloma</title>
            <link>http://www.medworm.com/index.php?rid=5000053&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F2nr3940832786552%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Despite the advantage observed with novel drugs such as bortezomib, thalidomide, or lenalidomide, multiple myeloma (MM) remains
 incurable and there is a clear need for new drugs or combinations based on the pathogenetic mechanism of MM. One of the proposed
 mechanisms in MM pathogenesis is the involvement of kinase molecules in the growth and survival of myelomatous cells. In this
 study, we have explored the optimal combination for dasatinib, a tyrosine kinase inhibitor, in MM cells. A clear synergistic
 effect was observed with the triple combination of dasatinib with bortezomib and dexamethasone which was evident even in the
 presence of bone marrow microenvironment. Experiments performed on freshly isolated patients’ cells also demonstrated potentiation
 of respo...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5000053</comments>
            <pubDate>Thu, 30 Jun 2011 09:38:42 +0100</pubDate>
            <guid isPermaLink="false">5000053</guid>        </item>
        <item>
            <title>Effects of tamibarotene for the treatment of adult T cell leukemia</title>
            <link>http://www.medworm.com/index.php?rid=5000054&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh3406uu84w5265r4%2F</link>
            <description>Content Type Journal ArticlePages 1-3DOI 10.1007/s00277-011-1290-4Authors
		Yasuhiro Maeda, Department of Hematology, National Hospital Organization Osaka Minami Medical Center, 2-1, Kidohigashi, Kawachinagano, Osaka, 586-8521 JapanMasaya Kawauchi, Department of Hematology, National Hospital Organization Osaka Minami Medical Center, 2-1, Kidohigashi, Kawachinagano, Osaka, 586-8521 JapanJun-ichi Miyatake, Department of Hematology, National Hospital Organization Osaka Minami Medical Center, 2-1, Kidohigashi, Kawachinagano, Osaka, 586-8521 JapanChikara Hirase, Department of Hematology, Kinki University School of Medicine, 377-2, Ohno-Higashi, Osaka, 589-8511 JapanTerufumi Yamaguchi, Department of Hematology, Kinki University School of Medicine, 377-2, Ohno-Higashi, Osaka, 589-8511 JapanItar...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5000054</comments>
            <pubDate>Thu, 30 Jun 2011 09:38:41 +0100</pubDate>
            <guid isPermaLink="false">5000054</guid>        </item>
        <item>
            <title>Phenotypic and genetic characterization of adult T-cell acute lymphoblastic leukemia with del(9)(q34);SET-NUP214 rearrangement</title>
            <link>http://www.medworm.com/index.php?rid=5000055&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fq2w277u36036t518%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;
 SET-NUP214 rearrangement is a recently recognized recurrent chromosomal translocation mostly observed in T-ALL. In order to characterize
 this rare entity, we performed phenotypic and genetic characterization of SET-NUP214 rearrangement through an investigation of a series of 40 consecutive samples of adult T-ALL that was selected among 229 adult
 ALL cases during 4&amp;nbsp;years in a single institution. Four cases (10%) of SET-NUP214 translocation were identified in our study. In all cases, diagnosis of T-ALL was established according to the World Health
 Organization (WHO) classification, and clonal TCR rearrangements were found. The immunophenotypic markers were indicative
 of the precursor nature of T lymphoblasts, and they expressed one or both of the myeloid-associ...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5000055</comments>
            <pubDate>Thu, 30 Jun 2011 09:38:39 +0100</pubDate>
            <guid isPermaLink="false">5000055</guid>        </item>
        <item>
            <title>The novel compound OSI-461 induces apoptosis and growth arrest in human acute myeloid leukemia cells</title>
            <link>http://www.medworm.com/index.php?rid=4994126&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F42u2g820u22g10jl%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Acute myeloid leukemia (AML) is a heterogeneous hematological malignancy. Treatment of patients suffering from high-risk AML
 as defined by clinical parameters, cytogenetics, and/or molecular analyses is often unsuccessful. OSI-461 is a pro-apoptotic
 compound that has been proposed as a novel therapeutic option for patients suffering from solid tumors like prostate or colorectal
 carcinoma. But little is known about its anti-proliferative potential in AML. Hence, we treated bone marrow derived CD34+ selected blast cells from 20 AML patients and the five AML cell lines KG-1a, THP-1, HL-60, U-937, and MV4-11 with the physiologically
 achievable concentration of 1&amp;nbsp;μM OSI-461 or equal amounts of DMSO as a control. Following incubation with OSI-461, we found
 a consis...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4994126</comments>
            <pubDate>Wed, 29 Jun 2011 10:51:05 +0100</pubDate>
            <guid isPermaLink="false">4994126</guid>        </item>
        <item>
            <title>Efficacy of an intensive post-induction chemotherapy regimen for adult patients with Philadelphia chromosome-negative acute lymphoblastic leukemia, given predominantly in the out-patient setting</title>
            <link>http://www.medworm.com/index.php?rid=4994127&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F13874u2619406496%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Intensification of chemotherapy in adults with acute lymphoblastic leukemia (ALL) has improved outcome. The aim of this analysis
 was to evaluate outcome of patients treated with an intensive regimen based on that used in the German national trials, but
 adapted in order to enable treatment to be given mainly on an out-patient basis, once complete remission (CR) had been achieved.
 Between 2000 and 2007, 53 patients with Philadelphia chromosome-negative ALL (40 with B-ALL and 13, T-ALL) received treatment.
 CR was achieved in 47/53 (89%), with no significant difference in CR rate between B- and T-ALL. At a median follow-up of 6.3&amp;nbsp;years,
 25 patients are alive, 23 (43%) in 1st CR, and 20 have relapsed. No patient died in CR due to treatment-related toxicity.
 At 5&amp;n...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4994127</comments>
            <pubDate>Tue, 28 Jun 2011 15:46:35 +0100</pubDate>
            <guid isPermaLink="false">4994127</guid>        </item>
        <item>
            <title>Postpartum anemia I: definition, prevalence, causes, and consequences</title>
            <link>http://www.medworm.com/index.php?rid=4986978&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fd321p73j1633gqk2%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;This review provides a status on the definition, prevalence, causes, and consequences of anemia in women who have given childbirth,
 i.e., postpartum anemia. The diagnosis of iron deficiency anemia relies on a full blood count including hemoglobin, serum
 ferritin, and serum soluble transferrin receptor, which appear to be reliable indicators of anemia and iron status 1&amp;nbsp;week
 postpartum while serum transferrin saturation is an unreliable indicator several weeks after delivery. It is recommended that
 postpartum anemia should be defined by hemoglobin &amp;lt;110&amp;nbsp;g/L at 1&amp;nbsp;week postpartum and &amp;lt;120&amp;nbsp;g/L at 8&amp;nbsp;weeks postpartum. The major
 causes of postpartum anemia are prepartum anemia combined with acute bleeding anemia due blood losses at delivery. N...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4986978</comments>
            <pubDate>Mon, 27 Jun 2011 17:50:54 +0100</pubDate>
            <guid isPermaLink="false">4986978</guid>        </item>
        <item>
            <title>Efficacy of rituximab in immune thrombocytopenic purpura: a retrospective survey</title>
            <link>http://www.medworm.com/index.php?rid=4986980&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb273r316072m0487%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;We conducted a retrospective survey to assess prescription practice, response rates to rituximab, and the predictive indicators
 for a response to rituximab therapy in patients with primary or secondary immune thrombocytopenic purpura (ITP). Data were
 collected retrospectively from 40 consecutive patients with ITP attending our hospital: 29 (72.5%) had primary ITP and 11
 (27.5%) had secondary ITP. Rituximab was given either as four weekly injections (375&amp;nbsp;mg/m2) or two injections of 1,000&amp;nbsp;mg given 2&amp;nbsp;weeks apart in 30 and 10 patients, respectively. The primary objective was to evaluate
 overall (OR) and complete response (CR) to rituximab therapy for ITP. OR was excellent and rapid and similar when secondary
 ITP was excluded from the analysis: OR was ach...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4986980</comments>
            <pubDate>Mon, 27 Jun 2011 17:50:52 +0100</pubDate>
            <guid isPermaLink="false">4986980</guid>        </item>
        <item>
            <title>Monitoring MRD with flow cytometry: an effective method to predict relapse for ALL patients after allogeneic hematopoietic stem cell transplantation</title>
            <link>http://www.medworm.com/index.php?rid=4986979&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk663t53881g16678%2F</link>
            <description>This study evaluated the prognostic value of minimal residual disease (MRD) monitoring by four-color flow cytometry (FCM)
 in patients with acute lymphoblastic leukemia (ALL) undergoing allogeneic hematopoietic stem cell transplantation (allo-HSCT).
 MRD was examined with four-color FCM at different time points in 139 patients (including pediatric and adult patients) with
 ALL after allo-HSCT. Real-time quantitative polymerase chain reaction (RQ-PCR) was applied to evaluate the MRD of Philadelphia
 chromosome-positive ALL (Ph+ ALL) patients. Patients who were FCM-positive (FCM+) after transplantation had a lower event-free
 survival (EFS) of 0.54 and a higher cumulative incidence of relapse (CIR) of 0.54 compared to an EFS of 0.80 and a CIR of
 0.08 in FCM-negative (FCM−) patients (EFS, ...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4986979</comments>
            <pubDate>Mon, 27 Jun 2011 17:50:52 +0100</pubDate>
            <guid isPermaLink="false">4986979</guid>        </item>
        <item>
            <title>Thalidomide, dexamethasone and lovastatin with autologous stem cell transplantation as a salvage immunomodulatory therapy in patients with relapsed and refractory multiple myeloma</title>
            <link>http://www.medworm.com/index.php?rid=4971169&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fx608217562467257%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The treatment of patients with multiple myeloma usually includes many drugs including thalidomide, lenalidomide and bortezomib.
 Lovastatin and other inhibitors of HMG-CoA reductase demonstrated to exhibit antineoplasmatic and proapoptotic properties
 in numerous in vitro studies involving myeloma cell lines. We treated 91 patients with relapsed or refractory multiple myeloma
 with thalidomide, dexamethasone and lovastatin (TDL group, 49 patients) or thalidomide and dexamethasone (TD group, 42 patients).
 A clinical response defined of at least 50% reduction of monoclonal band has been observed in 32% of TD patients and 44% of
 TDL patients. Prolongation of overall survival and progression-free survival in the TDL group as compared with the TD group
 has been documented...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4971169</comments>
            <pubDate>Wed, 22 Jun 2011 16:03:50 +0100</pubDate>
            <guid isPermaLink="false">4971169</guid>        </item>
        <item>
            <title>Efficacy and safety of micafungin as an empirical therapy for invasive fungal infections in patients with hematologic disorders: a multicenter, prospective study</title>
            <link>http://www.medworm.com/index.php?rid=4971170&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F568m02n85806g352%2F</link>
            <description>This study was conducted as a prospective, multicenter trial to evaluate the efficacy and safety of micafungin as an empirical
 therapy for suspected invasive fungal infections (IFIs), including febrile neutropenia (FN), and to evaluate the usefulness
 of β-d-glucan (BG) and Aspergillus galactomannan (GM) antigen in patients with hematologic diseases. A total of 121 patients were enrolled and assessed for
 safety, and 119 were examined for clinical efficacy. The main underlying diseases were acute myeloid leukemia (38.0%), acute
 lymphoblastic leukemia (18.2%), and malignant lymphoma (18.2%). The median initial daily dose and duration of micafungin treatment
 were 150&amp;nbsp;mg/day and 13&amp;nbsp;days, respectively. The overall response rate for suspected IFIs (n = 119), based on four comp...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4971170</comments>
            <pubDate>Tue, 21 Jun 2011 20:54:54 +0100</pubDate>
            <guid isPermaLink="false">4971170</guid>        </item>
        <item>
            <title>Acquired severe aplastic anemia after H1N1 influenza virus vaccination successfully treated with allogeneic bone marrow transplantation</title>
            <link>http://www.medworm.com/index.php?rid=4947054&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fw4j0401n523720kx%2F</link>
            <description>Content Type Journal ArticlePages 1-2DOI 10.1007/s00277-011-1278-0Authors
		Irene Donnini, Haematology Unit and Bone Marrow Trasplantation Section, University of Florence and Careggi Hospital, Largo Brambilla 3, 50134 Florence, ItalyBarbara Scappini, Haematology Unit and Bone Marrow Trasplantation Section, University of Florence and Careggi Hospital, Largo Brambilla 3, 50134 Florence, ItalyStefano Guidi, Haematology Unit and Bone Marrow Trasplantation Section, University of Florence and Careggi Hospital, Largo Brambilla 3, 50134 Florence, ItalyGiovanni Longo, Haematology Unit and Bone Marrow Trasplantation Section, University of Florence and Careggi Hospital, Largo Brambilla 3, 50134 Florence, ItalyAlberto Bosi, Haematology Unit and Bone Marrow Trasplantation Section, University of Flore...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4947054</comments>
            <pubDate>Fri, 17 Jun 2011 10:55:39 +0100</pubDate>
            <guid isPermaLink="false">4947054</guid>        </item>
        <item>
            <title>Prophylactic intravenous immunoglobulin during autologous haemopoietic stem cell transplantation for multiple myeloma is not associated with reduced infectious complications</title>
            <link>http://www.medworm.com/index.php?rid=4947055&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fr51g001506jk0041%2F</link>
            <description>In conclusion, our study did not show a benefit
 for the use of peri-transplant IVIG (0.4&amp;nbsp;g/kg) to reduce infectious complications in a large cohort of patients with myeloma
 undergoing ASCT. In the absence of data supporting efficacy in this context, there appears to be no benefit in the routine
 use of IVIG for this purpose.
 
 
	Content Type Journal ArticlePages 1-6DOI 10.1007/s00277-011-1275-3Authors
		Piers Blombery, Division of Cancer Medicine, Peter MacCallum Cancer Centre, East Melbourne, Melbourne, Victoria, AustraliaH. Miles Prince, Division of Cancer Medicine, Peter MacCallum Cancer Centre, East Melbourne, Melbourne, Victoria, AustraliaLeon J. Worth, Division of Cancer Medicine, Peter MacCallum Cancer Centre, East Melbourne, Melbourne, Victoria, AustraliaJo Main, Division o...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4947055</comments>
            <pubDate>Wed, 15 Jun 2011 06:18:54 +0100</pubDate>
            <guid isPermaLink="false">4947055</guid>        </item>
        <item>
            <title>Alterations of hemostatic parameters in the early development of allogeneic hematopoietic stem cell transplantation-related complications</title>
            <link>http://www.medworm.com/index.php?rid=4947056&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F1184436g3w5k482q%2F</link>
            <description>In this study, we investigated the early alterations of hemostatic
 parameters in allogeneic HSCT recipients and determined their potential diagnostic values in transplantation-related thrombotic
 complications and other post-HSCT events. Results from 107 patients with allogeneic HSCT showed higher levels of plasma plasminogen
 activator inhibitor-1 (PAI-1), fibrinogen, and tissue-plasminogen activator (t-PA) and a lower level of plasma protein C after
 transplantation. No change was found for prothrombin time, antithrombin III, d-dimer, and activated partial thromboplastin time following HSCT. Transplantation-related complications (TRCs) in HSCT patients
 were defined as thrombotic (n = 8), acute graft-versus-host disease (aGVHD, n = 45), and infectious (n = 38). All patients ...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4947056</comments>
            <pubDate>Wed, 15 Jun 2011 06:18:52 +0100</pubDate>
            <guid isPermaLink="false">4947056</guid>        </item>
        <item>
            <title>Risk of bleeding with oral anticoagulants: an updated systematic review and performance analysis of clinical prediction rules</title>
            <link>http://www.medworm.com/index.php?rid=4947057&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj45178523840818j%2F</link>
            <description>This study aimed to determine whether progress in developing bleeding risk estimation tools for patients on oral anticoagulant
 therapy has been made since 2006 when we last systematically reviewed this topic, and to refresh previously published quantitative
 evaluations of the clinical prediction rules (CPRs) available for estimating bleeding risk in patients on oral anticoagulant
 therapy. A systematic review of English language literature published since December 2006 was conducted when our previous
 systematic review ended. Studies were analyzed for predictive performance using likelihood ratios. Six studies detailed CPRs
 used to assess risk of bleeding prior to commencing warfarin therapy, four of which were included in the analysis. Three studies
 evaluated new CPRs (“RIETE” and...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4947057</comments>
            <pubDate>Tue, 14 Jun 2011 05:54:58 +0100</pubDate>
            <guid isPermaLink="false">4947057</guid>        </item>
        <item>
            <title>The impact of treatment, socio-demographic and clinical characteristics on health-related quality of life among Hodgkin’s and non-Hodgkin’s lymphoma survivors: a systematic review</title>
            <link>http://www.medworm.com/index.php?rid=4947058&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fa593781521150687%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Cancer survivors are at risk of experiencing adverse physical and psychosocial effects of their cancer and its treatment.
 Both Hodgkin’s lymphoma (HL) and non-Hodgkin’s lymphoma (NHL) survivors face problems that can affect their health-related
 quality of life (HRQoL). The authors systematically reviewed the literature on HRQoL among HL and NHL survivors. A PubMed
 and PsychINFO literature search for original articles published until May 2011 was performed. Twenty-four articles, which
 met the predefined inclusion criteria, were subjected to a quality checklist. HL survivors showed the most problems in (role)
 physical, social and cognitive functioning, general health, fatigue and financial problems. In addition, HL survivors treated
 with a combination of therapi...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4947058</comments>
            <pubDate>Tue, 14 Jun 2011 05:54:57 +0100</pubDate>
            <guid isPermaLink="false">4947058</guid>        </item>
        <item>
            <title>Mimicry of hydroxyurea-induced leg ulcer by distal vena saphena parva insufficiency</title>
            <link>http://www.medworm.com/index.php?rid=4914697&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F05178547322727r4%2F</link>
            <description>Content Type Journal ArticlePages 1-2DOI 10.1007/s00277-011-1270-8Authors
		Tobias Goerge, Department of Dermatology, University Hospital Muenster, Muenster, GermanyGuenther Schellong, Department of Pediatric Hematology and Oncology, Childrens University Hospital Muenster, Muenster, GermanyRolf M. Mesters, Department of Medicine—Hematology and Oncology, University Hospital Muenster, Albert—Schweitzerstreet 33, 48149 Muenster, GermanyWolfgang E. Berdel, Department of Medicine—Hematology and Oncology, University Hospital Muenster, Albert—Schweitzerstreet 33, 48149 Muenster, Germany
	

	
		Journal Annals of HematologyOnline ISSN 1432-0584Print ISSN 0939-5555 (Source: Annals of Hematology)</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4914697</comments>
            <pubDate>Mon, 06 Jun 2011 15:47:21 +0100</pubDate>
            <guid isPermaLink="false">4914697</guid>        </item>
        <item>
            <title>Low absolute lymphocyte count and addition of rituximab confer high risk for interstitial pneumonia in patients with diffuse large B-cell lymphoma</title>
            <link>http://www.medworm.com/index.php?rid=4914698&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fyr18030005153260%2F</link>
            <description>In conclusion, the incidence of IP is increased in patients
 with DLBCL receiving rituximab-containing chemotherapy. Specific subgroups with lymphopenia at diagnosis may justify close
 scrutiny to detect pulmonary complications.
 
 
	Content Type Journal ArticlePages 1-7DOI 10.1007/s00277-011-1268-2Authors
		Yu-Chung Huang, Division of Hematology and Oncology, Department of Medicine, Taipei Veterans General Hospital, No. 201, Sec. 2, Shipai Road, Taipei, 112 Taiwan, Republic of ChinaChia-Jen Liu, Division of Hematology and Oncology, Department of Medicine, Taipei Veterans General Hospital, No. 201, Sec. 2, Shipai Road, Taipei, 112 Taiwan, Republic of ChinaChun-Yu Liu, Division of Hematology and Oncology, Department of Medicine, Taipei Veterans General Hospital, No. 201, Sec. 2, Shipai Road...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4914698</comments>
            <pubDate>Mon, 06 Jun 2011 14:57:52 +0100</pubDate>
            <guid isPermaLink="false">4914698</guid>        </item>
        <item>
            <title>Lung injury in a leukemia patient during mobilization of peripheral blood stem cells using granulocyte colony-stimulating factor alone</title>
            <link>http://www.medworm.com/index.php?rid=4914700&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fnr57gn07g145380m%2F</link>
            <description>Content Type Journal ArticlePages 1-2DOI 10.1007/s00277-011-1264-6Authors
		Bing Shi, Department of Hematology, The 309th hospital of Chinese People’s Liberation Army, 17 Heishanhu Rd, Beijing, 100091 ChinaLihui Liu, Department of Hematology, The 309th hospital of Chinese People’s Liberation Army, 17 Heishanhu Rd, Beijing, 100091 ChinaLiping Ye, Department of Hematology, The 309th hospital of Chinese People’s Liberation Army, 17 Heishanhu Rd, Beijing, 100091 China
	

	
		Journal Annals of HematologyOnline ISSN 1432-0584Print ISSN 0939-5555 (Source: Annals of Hematology)</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4914700</comments>
            <pubDate>Mon, 06 Jun 2011 14:57:49 +0100</pubDate>
            <guid isPermaLink="false">4914700</guid>        </item>
        <item>
            <title>Lenalidomide is active for extramedullary disease in refractory multiple myeloma</title>
            <link>http://www.medworm.com/index.php?rid=4914699&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn222m3011qr14446%2F</link>
            <description>Content Type Journal ArticlePages 1-2DOI 10.1007/s00277-011-1272-6Authors
		Tomonori Nakazato, Department of Hematology, Yokohama Municipal Citizen’s Hospital, Yokohama, 56 Okazawa-cho, Hodogaya-ku, Yokohama, 240-8555 JapanAi Mihara, Department of Hematology, Yokohama Municipal Citizen’s Hospital, Yokohama, 56 Okazawa-cho, Hodogaya-ku, Yokohama, 240-8555 JapanChisako Ito, Department of Hematology, Yokohama Municipal Citizen’s Hospital, Yokohama, 56 Okazawa-cho, Hodogaya-ku, Yokohama, 240-8555 JapanYukinari Sanada, Department of Hematology, Yokohama Municipal Citizen’s Hospital, Yokohama, 56 Okazawa-cho, Hodogaya-ku, Yokohama, 240-8555 JapanYoshinobu Aisa, Department of Hematology, Yokohama Municipal Citizen’s Hospital, Yokohama, 56 Okazawa-cho, Hodogaya-ku, Yokohama, 240-8555 J...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4914699</comments>
            <pubDate>Mon, 06 Jun 2011 14:57:49 +0100</pubDate>
            <guid isPermaLink="false">4914699</guid>        </item>
        <item>
            <title>AL amyloidosis with severe gastrointestinal invasion and acute obstructive suppurative cholangitis</title>
            <link>http://www.medworm.com/index.php?rid=4914701&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F72r31323t404h4mk%2F</link>
            <description>Content Type Journal ArticlePages 1-2DOI 10.1007/s00277-011-1271-7Authors
		Yumiko Yoshiki, Department of Hematology and Oncology, Graduate School of Medicine, University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113–8655, JapanGo Yamamoto, Department of Hematology and Oncology, Graduate School of Medicine, University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113–8655, JapanYutaka Takazawa, Department of Pathology, Graduate School of Medicine, University of Tokyo, Tokyo, JapanYasuhito Nannya, Department of Hematology and Oncology, Graduate School of Medicine, University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113–8655, JapanJunichi Ishida, Department of Cardiovascular Medicine, Graduate School of Medicine, University of Tokyo, Tokyo, JapanRyozo Nagai, Department of Cardiovascular Medic...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4914701</comments>
            <pubDate>Sat, 04 Jun 2011 06:06:24 +0100</pubDate>
            <guid isPermaLink="false">4914701</guid>        </item>
        <item>
            <title>von Willebrand disease: a clinical and laboratory study of sixty-five patients</title>
            <link>http://www.medworm.com/index.php?rid=4914703&amp;cid=s_33273_19_f&amp;fid=33273&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn3353718k07n41uh%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;von Willebrand disease (VWD) is the commonest inherited bleeding disorder, yet it has not been well recognized in Southeast
 Asia. The aim of this prospective study was to report our experience of VWD diagnosis and to establish the clinical presentations
 of VWD in Taiwan. From October 2003 to April 2010, 863 patients with suspicion of having an inherited bleeding disorder underwent
 VWD screening tests. Those with positive tests were selected for further clinical and laboratory evaluation. A nested gender-
 and age-matched control cohort underwent similar investigation for comparison. VWD was diagnosed by comprehensive laboratory
 tests including factor VIII clotting activity, von Willebrand factor antigen assay, VWF:ristocetin cofactor activity (VWF:RCo)
 and platelet...</description>
            <author>Annals of Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4914703</comments>
            <pubDate>Sat, 04 Jun 2011 06:06:23 +0100</pubDate>
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            <title>Successful management with an effective induction regimen followed by allogeneic hematopoietic stem cell transplantation for promyelocytic blast crisis of chronic myelogenous leukemia</title>
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            <description>Content Type Journal ArticlePages 1-3DOI 10.1007/s00277-011-1269-1Authors
		Bo Cai, Department of Hematology, General Hospital of People’s Liberation Army, 28 Fuxing Road, Beijing, 100853 ChinaWeidong Yang, Department of Hematology, Hospital of Anyang District, Anyang, Henan, ChinaYu Zhao, Department of Hematology, General Hospital of People’s Liberation Army, 28 Fuxing Road, Beijing, 100853 ChinaLei Yuan, Department of Hematology, General Hospital of People’s Liberation Army, 28 Fuxing Road, Beijing, 100853 ChinaLili Wang, Department of Hematology, General Hospital of People’s Liberation Army, 28 Fuxing Road, Beijing, 100853 ChinaLi Gao, Department of Hematology, General Hospital of People’s Liberation Army, 28 Fuxing Road, Beijing, 100853 ChinaNan Wang, Department of Hematolo...</description>
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