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        <title>Acta Haematologica 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 'Acta Haematologica' source.</description>
        <link><![CDATA[http://www.medworm.com/rss/search.php?qu=Acta+Haematologica&t=Acta+Haematologica&s=Search&f=source]]></link>
        <lastBuildDate>Wed, 08 Feb 2012 17:41:55 +0100</lastBuildDate>
        <item>
            <title>Simultaneous Occurrence of Biphenotypic T Cell/Myeloid Lesions Involving t(12;13)(p13;q14) in a Pediatric Patient.</title>
            <link>http://www.medworm.com/index.php?rid=5664014&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22301888%26dopt%3DAbstract</link>
            <description>Authors: Carneiro Borba C, de Lourdes Chauffaille M, Saeed Sanabnai S, Folloni Fernandes J, Aiko Kumeda C, Rodrigues Pereira Velloso ED, Jarandilha Dos Santos K, Puato Vieira Pupim M, Hamerschlak N, Odone Filho V, Bendit I
    Abstract
    This paper chronicles a 2-year-old girl who presented with acute leukemia/lymphoma syndrome of the T cell immunophenotype. At this time, the cytogenetic analysis of her bone marrow cells showed a reciprocal translocation between the short arm of chromosome 12 and the long arm of chromosome 13, t(12;13)(p13;q14). The immunophenotyping of bone marrow blast cells by flow cytometry revealed a population of cells positive for CD56, CD117, CD45, partial CD33, partial HLA-DR, CD13, CD7, CD2 and CD5. Therefore, a diagnosis of acute leukemia with a mixed T cell/m...</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5664014</comments>
            <pubDate>Wed, 01 Feb 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5664014</guid>        </item>
        <item>
            <title>Acquired Hemophilia A in a Patient with Essential Thrombocythemia.</title>
            <link>http://www.medworm.com/index.php?rid=5664013&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22301942%26dopt%3DAbstract</link>
            <description>Authors: Mori N, Totsuka K, Ishimori N, Yoshinaga K, Teramura M, Noguchi S, Oda H, Motoji T
    Abstract
    A 69-year-old woman with essential thrombocythemia (ET) developed giant ecchymosis, and she was admitted to hospital. Marked anemia (Hb 8.1 g/dl) accompanied by a prolonged activated partial thromboplastin time (89.6 s) was observed, and she received red blood cells (RBC) and fresh frozen plasma (FFP). On day 2 after admission, consciousness disturbance suddenly occurred, whereas computed tomography of the brain showed no evidence of bleeding. As the ecchymosis progressed, she developed shock. Although RBC and FFP transfusions were administered, she developed multi-organ failure and died 48 h after admission. Low factor VIII activity (&amp;lt;1%) accompanied by factor VIII inhibitor (17...</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5664013</comments>
            <pubDate>Wed, 01 Feb 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5664013</guid>        </item>
        <item>
            <title>Effects of Exercise Training on Red Blood Cell Production: Implications for Anemia.</title>
            <link>http://www.medworm.com/index.php?rid=5664015&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22301865%26dopt%3DAbstract</link>
            <description>Authors: Hu M, Lin W
    Abstract
    Exercise training can increase total Hb and red cell mass, which enhances oxygen-carrying capacity. The possible underlying mechanisms are proposed to come mainly from bone marrow, including stimulated erythropoiesis with hyperplasia of the hematopoietic bone marrow, improvement of the hematopoietic microenvironment induced by exercise training, and hormone- and cytokine-accelerated erythropoiesis. Anemia is one of the most common medical conditions in chronic disease. The effects of exercise training on counteracting anemia have been explored and evaluated. The results of the research available to date are controversial, and it seems that significant methodological limitations exist. However, exercise training might be a promising, additional, safe an...</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5664015</comments>
            <pubDate>Tue, 31 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5664015</guid>        </item>
        <item>
            <title>Combining Nilotinib and Imatinib Improves the Outcome of Imatinib-Resistant Blast Phase CML.</title>
            <link>http://www.medworm.com/index.php?rid=5644311&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22286512%26dopt%3DAbstract</link>
            <description>Authors: Zhu GR, Ji O, Ji JM, Zhang YC, Wu Y, Yu H, Jiang PJ, Shen Q
    Abstract
    Imatinib resistance is an important hurdle in the treatment of chronic myeloid leukemia (CML), and CML patients with this drug resistance are often given a dismal prognosis. In this case report, an imatinib-refractory blast phase CML patient was treated with a combination of imatinib and nilotinib. A complete hematologic response was achieved within 3 months, the drug combination was well tolerated, and there was a relatively long bone-marrow complete remission. These results suggest that combining imatinib and nilotinib treatment may improve the outcome of imatinib-resistant CML patients in the blast phase. We hypothesize regarding the possible mechanism for the effectiveness of the drug combination by r...</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5644311</comments>
            <pubDate>Fri, 27 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5644311</guid>        </item>
        <item>
            <title>An Increased Number of Individuals with Clinically Recognized Monoclonal B-Cell Lymphocytosis Characterizes a Recent Database of Chronic Lymphocytic Leukemia Rai Stage 0.</title>
            <link>http://www.medworm.com/index.php?rid=5627332&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22262125%26dopt%3DAbstract</link>
            <description>Authors: Molica S, Gentile M, Mauro FR, Brugiatelli M, Federico M, Sperduti I, Neri A, Ferrarini M, Foà R, Morabito F
    Abstract
    No abstract available.
    PMID: 22262125 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5627332</comments>
            <pubDate>Thu, 19 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5627332</guid>        </item>
        <item>
            <title>Blastic Plasmacytoid Dendritic Cell Neoplasm without Cutaneous Lesion at Presentation: Case Report and Literature Review.</title>
            <link>http://www.medworm.com/index.php?rid=5607297&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22236870%26dopt%3DAbstract</link>
            <description>Authors: Wang H, Cao J, Hong X
    Abstract
    Blastic plasmacytoid dendritic cell neoplasm (BPDCN) is a rare and highly aggressive hematological malignancy derived from precursors of plasmacytoid dendritic cells. This disease typically presents with cutaneous involvement as the first manifestation, with subsequent or simultaneous spread to bone marrow and peripheral blood. It is exceedingly rare to diagnose BPDCN without a cutaneous lesion. Here, we report a 21-year-old male who was diagnosed with BPDCN in the absence of cutaneous symptoms. Clinically, left inguinal nodules were noticed for 4 months. The diagnosis of BPDCN was established based on histological and immunohistochemical study of a lymph node biopsy. The patient was classified as stage IVA with bone marrow involvement and un...</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5607297</comments>
            <pubDate>Thu, 12 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5607297</guid>        </item>
        <item>
            <title>Endoscopic Findings in Mantle Cell Lymphoma with Gastrointestinal Tract Involvement.</title>
            <link>http://www.medworm.com/index.php?rid=5607296&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22236942%26dopt%3DAbstract</link>
            <description>Conclusions: The endoscopic findings in GI MCL are variable, with common presenting manifestations of abdominal pain and GI bleeding.
    PMID: 22236942 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5607296</comments>
            <pubDate>Thu, 12 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5607296</guid>        </item>
        <item>
            <title>Prolonged Survival with Imatinib Mesylate Combined with Chemotherapy and Allogeneic Stem Cell Transplantation in de novo Ph+ Acute Myeloid Leukemia.</title>
            <link>http://www.medworm.com/index.php?rid=5607295&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22248505%26dopt%3DAbstract</link>
            <description>Conclusions: Our cases indicate that IM combined with daunorubicin-based chemotherapy followed by allo-HSCT and IM maintenance treatment is associated with a favorable outcome for de novo Ph+ AML, especially when IM is used in an early phase of AML.
    PMID: 22248505 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5607295</comments>
            <pubDate>Thu, 12 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5607295</guid>        </item>
        <item>
            <title>International Reporting Scale of BCR-ABL1 Fusion Transcript in Chronic Myeloid Leukemia: First Report from India.</title>
            <link>http://www.medworm.com/index.php?rid=5607294&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22249155%26dopt%3DAbstract</link>
            <description>In this report, we explain the process and steps involved in obtaining a valid lab-specific conversion factor for expressing BCR-ABL1 transcript levels in the IS.
    PMID: 22249155 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5607294</comments>
            <pubDate>Thu, 12 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5607294</guid>        </item>
        <item>
            <title>Submicroscopic Deletion of FGFR1 Gene Is Recurrently Detected in Myeloid and Lymphoid Neoplasms Associated with ZMYM2-FGFR1 Rearrangements: A Case Study.</title>
            <link>http://www.medworm.com/index.php?rid=5607298&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22236811%26dopt%3DAbstract</link>
            <description>Authors: Yang JJ, Park TS, Choi JR, Park SJ, Cho SY, Jun KR, Kim HR, Lee JN, Oh SH, Lee S, Kim B, Marschalek R, Meyer C
    Abstract
    No abstract available.
    PMID: 22236811 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5607298</comments>
            <pubDate>Wed, 11 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5607298</guid>        </item>
        <item>
            <title>Clonogenic Assays Are of Limited Value in Discriminating Patients with Myelodysplastic Syndrome and Patients with Megaloblastic Anemia.</title>
            <link>http://www.medworm.com/index.php?rid=5607299&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22236776%26dopt%3DAbstract</link>
            <description>Authors: Marisavljevic D
    Abstract
    No abstract available.
    PMID: 22236776 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5607299</comments>
            <pubDate>Sat, 07 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5607299</guid>        </item>
        <item>
            <title>Addition of Rituximab to High-Dose Methotrexate-Based Chemotherapy Improves Survival of Adults with Burkitt Lymphoma/Leukemia.</title>
            <link>http://www.medworm.com/index.php?rid=5568785&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22212303%26dopt%3DAbstract</link>
            <description>Authors: Dujmovic D, Aurer I, Radman I, Serventi-Seiwerth R, Dotlic S, Stern-Padovan R, Dubravcic K, Santek F, Labar B
    PMID: 22212303 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5568785</comments>
            <pubDate>Sat, 31 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5568785</guid>        </item>
        <item>
            <title>The Increased Risk for Pneumocystis Pneumonia in Patients Receiving Rituximab-CHOP-14 Can Be Prevented by the Administration of Trimethoprim/Sulfamethoxazole: A Single-Center Experience.</title>
            <link>http://www.medworm.com/index.php?rid=5538957&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22178955%26dopt%3DAbstract</link>
            <description>Authors: Hardak E, Oren I, Dann EJ, Yigla M, Faibish T, Rowe JM, Avivi I
    Abstract
    Recent studies suggest an increased risk for Pneumocystis jirovecii pneumonia (PJP) in adults receiving short-interval rituximab-CHOP (cyclophosphamide, doxorubicin, vincristine and prednisone) therapy for diffuse large cell B cell lymphoma (DLBCL). This retrospective study evaluates precise PJP incidence and the efficacy of anti-PJP prophylaxis in DLBCL. Patients with DLBCL, aged ≥18 years and treated between December 2004 and December 2010, were included. Details of treatment-related respiratory infections, focusing on PJP incidence, risk factors and prophylaxis, were assessed. A total of 132 patients were analyzed; 47 were treated with rituximab-CHOP therapy every 21 days (R-CHOP-21) and 85 were ...</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5538957</comments>
            <pubDate>Fri, 16 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5538957</guid>        </item>
        <item>
            <title>An Epstein-Barr Virus-Associated Leukemic Lymphoma in a Patient Treated with Rabbit Antithymocyte Globulin and Cyclosporine for Hepatitis-Associated Aplastic Anemia.</title>
            <link>http://www.medworm.com/index.php?rid=5538960&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22178718%26dopt%3DAbstract</link>
            <description>Authors: Ohata K, Iwaki N, Kotani T, Kondo Y, Yamazaki H, Nakao S
    Abstract
    Lymphoproliferative disorders (LPDs) are generally caused by uncontrolled B-cell proliferation induced by the Epstein-Barr virus (EBV) in the setting of impaired EBV-specific T-cell immunity, particularly when there is pharmacological immunosuppression including antithymocyte globulin. We herein present an unusual case of EBV associated with LPD (EBV-LPD) in which LPD occurred 3 weeks after the use of rabbit antithymocyte globulin administered for severe hepatitis-associated aplastic anemia; the patient died of fulminant leukemic lymphoma 5 days after the onset. We also review the pertinent literature on EBV-LPD after immunosuppressive therapy and document the efficacy of EBV viral load monitoring and the ne...</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5538960</comments>
            <pubDate>Thu, 15 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5538960</guid>        </item>
        <item>
            <title>Primary Thyroid Marginal Zone B-Cell Lymphoma of the Mucosa-Associated Lymphoid Tissue Type: Clinical Manifestation and Outcome of a Rare Disease - Consortium for Improving Survival of Lymphoma Study.</title>
            <link>http://www.medworm.com/index.php?rid=5538959&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22178776%26dopt%3DAbstract</link>
            <description>Conclusion: pTY-MZL tends to be an indolent disease. However, unlike other mucosa-associated lymphoid tissue site MZLs, pTY-MZL was well controlled via several treatment modalities, and the patients' responses were sustained for a prolonged period.
    PMID: 22178776 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5538959</comments>
            <pubDate>Thu, 15 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5538959</guid>        </item>
        <item>
            <title>Application of Mesenchymal Stromal Cells in Bone Marrow Transplantation for Sensitized Recipients.</title>
            <link>http://www.medworm.com/index.php?rid=5538958&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22178869%26dopt%3DAbstract</link>
            <description>Authors: Xu LH, Fang JP, Hong DL, Wu YF
    Abstract
    Sensitized patients are at high risk for graft rejection during transplantation. It is of interest to investigate the effect of mesenchymal stromal cells (MSCs) in sensitized hematopoietic stem cell transplantation. MSCs were generated from bone marrow cells of BALB/c mice. The molecular markers of MSCs were detected by flow cytometry. MSCs labeled with green fluorescent dye were transplanted into nonsensitized and sensitized recipients, respectively. Homing of MSCs in vivo was monitored at different time points post-transplantation. Additionally, sensitized BALB/c mice under irradiation were transplanted with syngeneic MSCs and allogeneic bone marrow cells, and the rate of survival was monitored daily. The fourth passage of MSCs pre...</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5538958</comments>
            <pubDate>Thu, 15 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5538958</guid>        </item>
        <item>
            <title>Richter Syndrome and Brain Involvement: Low-Grade Lymphoma Relapsing as Cerebral High-Grade Lymphoma.</title>
            <link>http://www.medworm.com/index.php?rid=5538971&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22156510%26dopt%3DAbstract</link>
            <description>This report extends the literature of central nervous system RS and particularly highlights the importance of a thorough diagnostic evaluation of patients with low-grade NHL presenting with neurological symptoms.
    PMID: 22156510 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5538971</comments>
            <pubDate>Sat, 10 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5538971</guid>        </item>
        <item>
            <title>Does Hypereosinophilic Syndrome Precede Common B Acute Lymphoblastic Leukaemia in Childhood? A Case Report.</title>
            <link>http://www.medworm.com/index.php?rid=5539008&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22156491%26dopt%3DAbstract</link>
            <description>Authors: Ayhan AC, Timur C, Ayhan Y, Cakır B, Erguven M
    Abstract
    Hypereosinophilic syndrome (HES) and the association of hypereosinophilia with acute lymphoblastic leukaemia (ALL) are both rare in children. Some acute myelogenous leukaemias can present with eosinophilia, but the relationship between HES and ALL is not well known and is rarer than the relationship between HES and acute myelogenous leukaemia. Patients are diagnosed with HES when no cause is found to explain the eosinophilia leading to end organ damage. For this reason, it is recommended that patients presenting with hypereosinophilia be carefully assessed to exclude any malignant clonal proliferation. HES may present with severe clinical manifestations such as high leucocyte count, anaemia, thrombocytopaenia, hepato...</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5539008</comments>
            <pubDate>Tue, 06 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5539008</guid>        </item>
        <item>
            <title>Comparable Analysis of Outcomes for Allogeneic Peripheral Blood Stem Cell Transplantation from Matched Related and Matched Unrelated Donors in Acute Myeloid Leukemia.</title>
            <link>http://www.medworm.com/index.php?rid=5496791&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22143083%26dopt%3DAbstract</link>
            <description>In conclusion, the allogeneic PBSCT outcomes for AML were comparable in the matched related and matched unrelated groups. Nonetheless, for high-risk AML patients, matched unrelated PBSCT was found to be preferable to matched related PBSCT.
    PMID: 22143083 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5496791</comments>
            <pubDate>Tue, 06 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5496791</guid>        </item>
        <item>
            <title>4G/5G Polymorphism of the Plasminogen Activator Inhibitor-1 Gene Is Associated with Multiple Organ Dysfunction in Critically Ill Patients.</title>
            <link>http://www.medworm.com/index.php?rid=5496792&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22134139%26dopt%3DAbstract</link>
            <description>Conclusions: These results demonstrate that the 4G/5G polymorphism of the PAI-1 gene affects the plasma PAI-1 concentration, which could impair fibrinolysis and cause organ failure, and thus the presence of the 4G allele increases the risk of death.
    PMID: 22134139 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5496792</comments>
            <pubDate>Tue, 29 Nov 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5496792</guid>        </item>
        <item>
            <title>Clinical Implications of Non-A-Type NPM1 and FLT3 Mutations in Patients with Normal Karyotype Acute Myeloid Leukemia.</title>
            <link>http://www.medworm.com/index.php?rid=5496793&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22104247%26dopt%3DAbstract</link>
            <description>Authors: Park BG, Chi HS, Park SJ, Min SK, Jang S, Park CJ, Kim DY, Lee JH, Lee JH, Lee KH
    Abstract
    Mutations in the nucleophosmin (NPM1) and fms-like tyrosine kinase-3 (FLT3) genes are the most commonly observed mutations in patients with normal-karyotype acute myeloid leukemia (AML-NK). We analyzed the prognostic effects and interactions of these mutations in 201 AML-NK patients. NPM1 and FLT3 mutations were found in 38.3 and 24.9% of AML-NK patients, respectively. NPM1 mutations (NPM1mut), especially in patients without FLT3 mutations (FLT3mut), were associated with a favorable outcome. However, NPM1mut did not affect survival. FLT3mut tended to be associated with a poor survival outcome. FLT3mut showed no prognostic effects in patients with A-type NPM1mut. However, FLT3mut were...</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5496793</comments>
            <pubDate>Fri, 18 Nov 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5496793</guid>        </item>
        <item>
            <title>Dasatinib Overrides Imatinib Resistance Mediated by the F359I Residue Mutation in Two Patients with Chronic Myeloid Leukemia.</title>
            <link>http://www.medworm.com/index.php?rid=5428231&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22094354%26dopt%3DAbstract</link>
            <description>Authors: Serpa M, Sanabani SS, Dorlhiac-Llacer PE, Nardinelli L, de Barros Ferreira P, Borges Martins TF, Seguro F, Bendit I
    Abstract
    Despite the beneficial effects of imatinib mesylate, some patients may either not respond or respond suboptimally. Here, we report two chronic myelogenous leukemia patients; one had a suboptimal response according to European LeukemiaNet criteria (a major molecular response was not achieved after 18 months of standard-dose imatinib therapy) and the other had failure with a standard dose of imatinib. At the time of the suboptimal response in patient 1 and the failure in patient 2, we were able to detect the F359I mutation in the BCR-ABL tyrosine kinase domain using DNA sequencing in both patients. Therefore, it was decided to change the therapeutic re...</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5428231</comments>
            <pubDate>Thu, 17 Nov 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5428231</guid>        </item>
        <item>
            <title>High-Risk Acute Promyelocytic Leukemia with Early Differentiation Syndrome: A Therapeutic Dilemma.</title>
            <link>http://www.medworm.com/index.php?rid=5428230&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22094378%26dopt%3DAbstract</link>
            <description>Authors: Malato A, Santoro A, Felice R, Magrin S, Turri D, Bica MG, Salemi D, Fabbiano F
    PMID: 22094378 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5428230</comments>
            <pubDate>Thu, 17 Nov 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5428230</guid>        </item>
        <item>
            <title>Practical Diagnosis of Red Cell Disorders in Southern Spain.</title>
            <link>http://www.medworm.com/index.php?rid=5383475&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22042243%26dopt%3DAbstract</link>
            <description>Conclusion: Given the modern migratory flows, greater knowledge of these disorders is needed by all medical staff, and new practical and cost/time-effective diagnostic approaches have to be devised.
    PMID: 22042243 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5383475</comments>
            <pubDate>Tue, 25 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5383475</guid>        </item>
        <item>
            <title>Coexistence of JAK2V617F Mutation and BCR-ABL1 Transcript in Two Chinese Patients with Chronic Myelogenous Leukemia.</title>
            <link>http://www.medworm.com/index.php?rid=5348213&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22025110%26dopt%3DAbstract</link>
            <description>Authors: Xiao X, Zhang Y, Zhang GS, Zheng WL, Xiao L, Liu SF
    Abstract
    No abstract available.
    PMID: 22025110 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5348213</comments>
            <pubDate>Wed, 19 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5348213</guid>        </item>
        <item>
            <title>Submicroscopic Deletion of RUNX1T1 Gene Confirmed by High-Resolution Microarray in Acute Myeloid Leukemia with RUNX1/RUNX1T1 Rearrangement.</title>
            <link>http://www.medworm.com/index.php?rid=5348214&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22025082%26dopt%3DAbstract</link>
            <description>Authors: Yang JJ, Oh SH, Cho SY, Suh JT, Lee HJ, Lee WI, Lee J, Baek SK, Yoon HJ, Cho EH, Park TS
    Abstract
    No abstract available.
    PMID: 22025082 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5348214</comments>
            <pubDate>Tue, 18 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5348214</guid>        </item>
        <item>
            <title>Additional Chromosome Abnormalities, BCR-ABL Tyrosine Kinase Domain Mutations and Clinical Outcome in Hungarian Tyrosine Kinase Inhibitor-Resistant Chronic Myelogenous Leukemia Patients.</title>
            <link>http://www.medworm.com/index.php?rid=5348215&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22005133%26dopt%3DAbstract</link>
            <description>Conclusion: For patients with TKI resistance, mutation and ACA screening may play a role in identifying patients with poorer prognosis.
    PMID: 22005133 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5348215</comments>
            <pubDate>Fri, 14 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5348215</guid>        </item>
        <item>
            <title>Glutathionyl Hemoglobin Is Elevated in Iron Deficiency Anemia.</title>
            <link>http://www.medworm.com/index.php?rid=5348217&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21996674%26dopt%3DAbstract</link>
            <description>Authors: Shet AS, Pinto SM, Mitra G, Mandal AK
    Abstract
    There are few good biomarkers of iron deficiency anemia (IDA). Since IDA patients have evidence for increased oxidative stress, we used mass spectrometry (MS) [i.e. matrix-assisted laser desorption/ionization (MALDI) and electrospray ionization] to identify novel biomarkers. Using MALDI-MS, the following oxidative modifications of hemoglobin with the following mass-to-charge ratios were identified: 1,087.5 (α32-40), 1,545.7 (α17-31), 1,290.0 (β31-40) and 2,076.1 (β41-59). On electrospray ionization MS, the IDA patients had significantly elevated glutathionyl hemoglobin (GSHb) compared with the controls (16.9 ± 9.6 vs. 7.7 ± 3.7%; p = 0.002). GSHb levels correlated inversely with serum ferritin (Spearman rho -0.485; p = 0...</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5348217</comments>
            <pubDate>Thu, 13 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5348217</guid>        </item>
        <item>
            <title>The Defined Daily Doses of Low Molecular Weight Heparins Do Not Reflect Current Clinical Practice.</title>
            <link>http://www.medworm.com/index.php?rid=5348216&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21996727%26dopt%3DAbstract</link>
            <description>Authors: Jorgensen LN, Gewert K
    Abstract
    No abstract available.
    PMID: 21996727 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5348216</comments>
            <pubDate>Thu, 13 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5348216</guid>        </item>
        <item>
            <title>Efficacy of Low-Dose Rituximab in a Refractory Acquired Factor VIII Inhibitor Case Secondary to Pemphigus.</title>
            <link>http://www.medworm.com/index.php?rid=5348219&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21996575%26dopt%3DAbstract</link>
            <description>In conclusion, our results indicate that low-dose rituximab might be an effective and safe treatment for patients with acquired FVIII inhibitor.
    PMID: 21996575 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5348219</comments>
            <pubDate>Wed, 12 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5348219</guid>        </item>
        <item>
            <title>Internal Iliac Artery Perforation following Bone Marrow Aspiration in a Patient with No Previously Identified Risk Factors: A Case Report and Review of the Literature.</title>
            <link>http://www.medworm.com/index.php?rid=5348218&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21996611%26dopt%3DAbstract</link>
            <description>Authors: Martino M, Console G, Russo L, Messina G, D'Arro' BL, Irrera G, Barreca G
    Abstract
    No abstract available.
    PMID: 21996611 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5348218</comments>
            <pubDate>Wed, 12 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5348218</guid>        </item>
        <item>
            <title>Successful Treatment of Chemotherapy-Refractory Angioimmunoblastic T Cell Lymphoma with Cyclosporin A.</title>
            <link>http://www.medworm.com/index.php?rid=5348221&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21986307%26dopt%3DAbstract</link>
            <description>This report concerns the effect of cyclosporin A (CsA) on chemotherapy-refractory AITL. A 68-year-old female with AITL with systemic symptoms, such as high fever, skin rash andgeneralized lymphadenopathy, was initially treated with conventional cytotoxic chemotherapies using alkylators, anthracyclines and corticosteroids, which failed to induce remission. However, CsA (4 mg/kg/day) plus dexamethasone treatment resulted in a dramatic regression of the tumors and amelioration of systemic symptoms and induced complete remission (CR) within 2 weeks. Currently, the patient's CR has continued for more than 18 months with CsA maintenance therapy. Our experience and previously reported findings suggest that CsA may constitute an alternative treatment option for AITL, even though the use of convent...</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5348221</comments>
            <pubDate>Fri, 07 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5348221</guid>        </item>
        <item>
            <title>Fast Approach for Clarification of Chromosomal Aberrations by Using LM-PCR and FT-CGH in Leukaemic Sample.</title>
            <link>http://www.medworm.com/index.php?rid=5348220&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21986343%26dopt%3DAbstract</link>
            <description>Authors: Dittmann K, Przybylski GK, Grabarczyk P, Dölken G, Gesk S, Siebert R, Schmidt CA
    Abstract
    Chromosomal abnormalities, like deletions, amplifications, inversions or translocations, are recurrent features in haematological malignancies. However, the precise molecular breakpoints are frequently not determined. Here we describe a rapid analysis of genetic imbalances combining fine tiling comparative genomic hybridization (FT-CGH) and ligation-mediated PCR (LM-PCR). We clarified an inv(14)(q11q32) in a case of T cell acute lymphoblastic leukaemia with a breakpoint in the TRA/D in 68% of cells detected by fluorescence in situ hybridization. FT-CGH showed several mono- and biallelic losses within TRA/D. LM-PCR disclosed a TRA/D rearrangement on one allele. The other allele reveal...</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5348220</comments>
            <pubDate>Fri, 07 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5348220</guid>        </item>
        <item>
            <title>The Oral Iron Chelator Deferasirox Induces Apoptosis in Myeloid Leukemia Cells by Targeting Caspase.</title>
            <link>http://www.medworm.com/index.php?rid=5284277&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21951998%26dopt%3DAbstract</link>
            <description>Authors: Kim JL, Kang HN, Kang MH, Yoo YA, Kim JS, Choi CW
    Abstract
    No abstract available.
    PMID: 21951998 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5284277</comments>
            <pubDate>Tue, 27 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5284277</guid>        </item>
        <item>
            <title>Acute Myeloid Leukemia Unlikely Related to Trabectedin Treatment.</title>
            <link>http://www.medworm.com/index.php?rid=5284275&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21952689%26dopt%3DAbstract</link>
            <description>Authors: Cartoafa M, Kahatt C, Soto-Matos A, Roy E, Lardelli P
    Abstract
    No abstract available.
    PMID: 21952689 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5284275</comments>
            <pubDate>Sat, 24 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5284275</guid>        </item>
        <item>
            <title>Reply.</title>
            <link>http://www.medworm.com/index.php?rid=5284274&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21952727%26dopt%3DAbstract</link>
            <description>Authors: Liu SV, Douer D
    Abstract
    No abstract available.
    PMID: 21952727 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5284274</comments>
            <pubDate>Sat, 24 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5284274</guid>        </item>
        <item>
            <title>Unusual Course of Myelodysplastic Syndrome with Presumed Familial Origin.</title>
            <link>http://www.medworm.com/index.php?rid=5284276&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21952642%26dopt%3DAbstract</link>
            <description>Authors: Bacher U, Ocheni S, Schafhausen P, Oyekunle A, Dierlamm J, Zander AR, Bokemeyer C, Haferlach T, Kröger N
    Abstract
    No abstract available.
    PMID: 21952642 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5284276</comments>
            <pubDate>Thu, 22 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5284276</guid>        </item>
        <item>
            <title>Cytokine-Induced Apoptosis of Beta-Thalassemia/Hemoglobin E Erythroid Progenitor Cells via Nitric Oxide-Mediated Process in vitro.</title>
            <link>http://www.medworm.com/index.php?rid=5249688&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21934298%26dopt%3DAbstract</link>
            <description>Conclusion: The marked sensitivity of erythroid progenitor cells from β-thal/HbE patients to cytokine-induced apoptosis via an NO-mediated process reflects a proapoptotic status of such thalassemic red blood cells.
    PMID: 21934298 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5249688</comments>
            <pubDate>Wed, 21 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5249688</guid>        </item>
        <item>
            <title>Safety and Efficacy of Combination Therapy with Pegylated Interferon Alpha-2a and Ribavirin in Treating Patients with Chronic Hepatitis C and Beta-Thalassaemia Major: A Greek Single-Center Experience.</title>
            <link>http://www.medworm.com/index.php?rid=5249687&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21934299%26dopt%3DAbstract</link>
            <description>Authors: Paschos P, Vlachaki E, Pasvanti C, Sinakos E, Kalpaka A, Klonizakis P, Perifanis V
    Abstract
    No abstract available.
    PMID: 21934299 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5249687</comments>
            <pubDate>Wed, 21 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5249687</guid>        </item>
        <item>
            <title>The PML Gene of the PML-RARα V-Form Fusion Transcript Breaks within Exon 6.</title>
            <link>http://www.medworm.com/index.php?rid=5249690&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21934296%26dopt%3DAbstract</link>
            <description>Authors: Qi X, Tan Y, Chen X, Bian S, Zhang L, Xu A, Xu Z, Wang H
    Abstract
    No abstract available.
    PMID: 21934296 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5249690</comments>
            <pubDate>Tue, 20 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5249690</guid>        </item>
        <item>
            <title>Occurrence of BCR-ABL1-Positive Chronic Myeloid Leukemia following Essential Thrombocythemia.</title>
            <link>http://www.medworm.com/index.php?rid=5249689&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21934297%26dopt%3DAbstract</link>
            <description>Authors: Weng WH, Shih LY
    PMID: 21934297 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5249689</comments>
            <pubDate>Tue, 20 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5249689</guid>        </item>
        <item>
            <title>BRIT1/MCPH1 Expression in Chronic Myeloid Leukemia and Its Regulation of the G2/M Checkpoint.</title>
            <link>http://www.medworm.com/index.php?rid=5249693&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21934293%26dopt%3DAbstract</link>
            <description>In conclusion, we found that CML cells have a low BRIT1/MCPH1 level and show a defective G2/M arrest, confirming that these cells have a constitutive genomic instability.
    PMID: 21934293 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5249693</comments>
            <pubDate>Fri, 16 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5249693</guid>        </item>
        <item>
            <title>Severe Acquired Neutropenia Associated with Anti-Proteinase 3 Antibodies.</title>
            <link>http://www.medworm.com/index.php?rid=5249692&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21934294%26dopt%3DAbstract</link>
            <description>Authors: Loschi M, Jouen F, Kerleau JM, Tilly H, Jardin F
    Abstract
    No abstract available.
    PMID: 21934294 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5249692</comments>
            <pubDate>Fri, 16 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5249692</guid>        </item>
        <item>
            <title>Acute Lymphoblastic Leukaemia with an e1a3 BCR-ABL1 Fusion.</title>
            <link>http://www.medworm.com/index.php?rid=5249691&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21934295%26dopt%3DAbstract</link>
            <description>Authors: Langabeer SE, Haslam K, Kelly J, Leahy M, Vandenberghe E
    Abstract
    No abstract available.
    PMID: 21934295 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5249691</comments>
            <pubDate>Fri, 16 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5249691</guid>        </item>
        <item>
            <title>Candida albicans-Induced Chronic Thrombocytopenic Purpura.</title>
            <link>http://www.medworm.com/index.php?rid=5160408&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21860227%26dopt%3DAbstract</link>
            <description>We present 2 patients with chronic immune thrombocytopenic purpura (ITP) secondary to Candida albicans infection. Neither patient responded to standard ITP therapy including splenectomy. Appropriate antifungal treatment of the C. albicans infection was followed by sustained improvement in platelet count in both patients. To our knowledge, this is the first report of ITP in association with C. albicans infection.
    PMID: 21860227 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5160408</comments>
            <pubDate>Mon, 22 Aug 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5160408</guid>        </item>
        <item>
            <title>Complete Remission with a Combination of Lenalidomide, Cyclophosphamide and Prednisolone in a Patient with Incomplete POEMS Syndrome.</title>
            <link>http://www.medworm.com/index.php?rid=5142975&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21849771%26dopt%3DAbstract</link>
            <description>Authors: Suyanı E, Yağcı M, Sucak GT
    Abstract
    No abstract available.
    PMID: 21849771 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5142975</comments>
            <pubDate>Wed, 17 Aug 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5142975</guid>        </item>
        <item>
            <title>De novo Acute Myeloid Leukemia Associated with t(11;17)(q23;q25) and MLL-SEPT9 Rearrangement in an Elderly Patient: A Case Study and Review of the Literature.</title>
            <link>http://www.medworm.com/index.php?rid=5142976&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21846973%26dopt%3DAbstract</link>
            <description>Authors: Lee SG, Park TS, Oh SH, Park JC, Yang YJ, Marschalek R, Meyer C, Cho EH, Shin SY
    Abstract
    No abstract available.
    PMID: 21846973 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5142976</comments>
            <pubDate>Mon, 15 Aug 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5142976</guid>        </item>
        <item>
            <title>The Incidence and Survival of Acute de novo Leukemias in Estonia and in a Well-Defined Region of Western Sweden during 1997-2001: A Survey of Patients Aged 16-64 Years.</title>
            <link>http://www.medworm.com/index.php?rid=5142978&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21846971%26dopt%3DAbstract</link>
            <description>Conclusion: In Estonia, a remarkable improvement in outcome for young de novo AL patients was seen after 1996. Nevertheless, relative survival for the Estonian patients had still not reached the levels found in the Swedish cohort.
    PMID: 21846971 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5142978</comments>
            <pubDate>Fri, 12 Aug 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5142978</guid>        </item>
        <item>
            <title>Classical Hairy Cell Leukemia and Its Variant: A 17-Year Retrospective Survey in Taiwan Chinese.</title>
            <link>http://www.medworm.com/index.php?rid=5142977&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21846972%26dopt%3DAbstract</link>
            <description>Conclusion: A relatively higher proportion of HCL-V in all HCL comparing to Westerners is observed. Second malignancies are common. With an inferior outcome and dismal response to most treatment, enrollment in a clinical trial should be considered for HCL-V.
    PMID: 21846972 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5142977</comments>
            <pubDate>Fri, 12 Aug 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5142977</guid>        </item>
        <item>
            <title>Helicobacter pylori Upregulates Peripheral Platelet Counts Mainly in Female Patients.</title>
            <link>http://www.medworm.com/index.php?rid=5113122&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21811059%26dopt%3DAbstract</link>
            <description>In conclusion, H. pylori infection upregulates platelet counts mainly in females, and eradication reduced peripheral platelets in both sexes. Females appeared more susceptible to H. pylori infection than males with regard to upregulation of platelet counts.
    PMID: 21811059 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5113122</comments>
            <pubDate>Fri, 29 Jul 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5113122</guid>        </item>
        <item>
            <title>JAK2 Mutation-Negative Secondary Erythrocytosis in Smoldering Plasma Cell Myeloma: A Case Study and Review of the Literature.</title>
            <link>http://www.medworm.com/index.php?rid=5113123&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21791913%26dopt%3DAbstract</link>
            <description>Authors: Lee SG, Lim G, Cho SY, Suh JT, Lee HJ, Baek SK, Lee WI, Yoon HJ, Park TS
    No abstract available.
    PMID: 21791913 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5113123</comments>
            <pubDate>Tue, 26 Jul 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5113123</guid>        </item>
        <item>
            <title>A Systematic Review on the Use of Bortezomib in Multiple Myeloma Patients with Renal Impairment: What Is the Published Evidence?</title>
            <link>http://www.medworm.com/index.php?rid=5113124&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21778706%26dopt%3DAbstract</link>
            <description>This report presents the totality of evidence through a systematic review that assessed either the efficacy or safety of bortezomib-based regimens in multiple myeloma with renal impairment. A systematic and comprehensive search of the literature was performed using MEDLINE databases from 1978 to December 1, 2010, and a hand search of references. We used the following medical subject headings (MESH) to identify potential studies: 'myeloma renal failure' (1,225 hits) and 'bortezomib' (2,554 hits). An additional search performed by combining the MESH terms 'myeloma renal failure' and 'bortezomib' yielded 50 citations. Five additional case-control studies judged relevant for the purpose of study were also included. In total, 6 case reports, 9 case series and 9 case-control studies were identif...</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5113124</comments>
            <pubDate>Wed, 20 Jul 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5113124</guid>        </item>
        <item>
            <title>Lactate Dehydrogenase and Severity of Pain in Children with Sickle Cell Disease.</title>
            <link>http://www.medworm.com/index.php?rid=5113125&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21778705%26dopt%3DAbstract</link>
            <description>Conclusion: From this study it can be concluded that LDH is a significant biochemical marker for the severity of pain during a vaso-occlusive episode in SCD.
    PMID: 21778705 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5113125</comments>
            <pubDate>Tue, 19 Jul 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5113125</guid>        </item>
        <item>
            <title>Successful Treatment of Autoimmune Hemolytic Anemia Associated with Multicentric Castleman Disease by Anti-Interleukin-6 Receptor Antibody (Tocilizumab) Therapy.</title>
            <link>http://www.medworm.com/index.php?rid=5113128&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21757886%26dopt%3DAbstract</link>
            <description>We describe herein the successful treatment of severe autoimmune hemolytic anemia (AIHA) in a patient with multicentric Castleman disease (MCD) by humanized anti-interleukin-6 (IL-6) receptor antibody (tocilizumab) therapy. Inflammatory anemia is commonly reported; however, AIHA is a very rare complication of MCD. In 1996, a 45-year-old Japanese woman was referred to our hospital because of generalized lymphadenopathy, anemia and skin eruptions. Lymph node biopsy demonstrated MCD. She was treated with prednisolone (1 mg/kg/day), which improved the anemia and skin eruptions. In 2009, she suddenly developed Coombs-positive hemolytic anemia. The blood count was as follows: hemoglobin 4.7 g/dl, platelets 490 × 10(9)/l and white blood cell count 9.8 × 10(9)/l. Both direct and indirect Coombs'...</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5113128</comments>
            <pubDate>Wed, 13 Jul 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5113128</guid>        </item>
        <item>
            <title>Professor Georgi D. Efremov (1932-2011).</title>
            <link>http://www.medworm.com/index.php?rid=5113127&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21757887%26dopt%3DAbstract</link>
            <description>Authors: Plaseska-Karanfilska D, Dimovski A
    
    PMID: 21757887 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5113127</comments>
            <pubDate>Wed, 13 Jul 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5113127</guid>        </item>
        <item>
            <title>Acute Promyelocytic Leukemia with a Smoldering Course Associated with Therapy-Related Myelodysplastic Syndrome.</title>
            <link>http://www.medworm.com/index.php?rid=5113126&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21757888%26dopt%3DAbstract</link>
            <description>We describe a 67-year-old female patient who presented with an atypical course of tAPL. Atypical features in this patient's course included a preceding therapy-related myelodysplastic syndrome (MDS) with a slowly expanding pathological promyelocyte clone. Following treatment with all-trans-retinoic acid and arsenic trioxide, the patient achieved complete clinical, morphological and molecular remission. Review of the pertinent literature highlights the rarity of MDS transforming into APL, although dysplasia has been shown to be a possible feature of tAPL. MDS may be an underdiagnosed stage in tAPL leukomogenesis. This case also underscores the complexity of clinical decision-making in the context of tAPL.
    PMID: 21757888 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5113126</comments>
            <pubDate>Wed, 13 Jul 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5113126</guid>        </item>
        <item>
            <title>Diffuse Large B Cell Lymphoma Complicating Total Knee Arthroplasty: Case Report and Literature Review of the Association of Diffuse Large B Cell Lymphoma with Joint Replacement.</title>
            <link>http://www.medworm.com/index.php?rid=5019539&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21734365%26dopt%3DAbstract</link>
            <description>Authors: Chaudhry MS, Mather H, Marks A, Naresh K
    Primary lymphoma of bone is extremely rare. There are increasing reports of lymphoma arising in bone adjacent to metallic prostheses. Herein, we describe the case of a 76-year-old man who developed diffuse large B cell lymphoma in the tibia 3 years after total knee arthroplasty for osteoarthritis. A review of the literature has identified 11 other cases of lymphoma arising in the context of orthopaedic metallic implants. To our knowledge this is the first reported case of a primary lymphoma arising in bone adjacent to a knee prosthesis. Possible pathogenetic mechanisms may include chronic antigenic stimulation of lymphocytes, proliferation of EBV-infected B lymphocytes, and direct mutagenic effects of metallic ions. Further research is ...</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5019539</comments>
            <pubDate>Wed, 06 Jul 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5019539</guid>        </item>
        <item>
            <title>Blastic Plasmacytoid Dendritic Cell Neoplasm Expressing the CD13 Myeloid Antigen.</title>
            <link>http://www.medworm.com/index.php?rid=5019543&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21701157%26dopt%3DAbstract</link>
            <description>We present a case of an 80-year-old man with a CD4+CD56+ BPDCN that affected the orbital cavity and bone marrow. Although BPDCN has not been reported to express any lineage-specific markers, the neoplastic cells strongly expressed the CD13 antigen. Therefore, in addition to pathological examination, we attempted to induce in vitro morphological and surface marker changes with IL-3 and CD40 ligand. After treatment with these cytokines, the tumor cells enlarged markedly, acquired many fine dendrites, similar to mature DC, and showed enhanced expression of antigens specific to DC or antigen-presenting cells, such as CD40, CD80, CD83 and CD86. To the best of our knowledge, this is the first report of BPDCN expressing a myeloid antigen, CD13, although CD33 expression has been described in some ...</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5019543</comments>
            <pubDate>Thu, 23 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5019543</guid>        </item>
        <item>
            <title>Unusually Long Survival of a 67-Year-Old Patient with Near-Tetraploid Acute Myeloid Leukemia M0 without Erythroblastic and Megakaryocytic Dysplasia.</title>
            <link>http://www.medworm.com/index.php?rid=5019542&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21701158%26dopt%3DAbstract</link>
            <description>We present the case of a 67-year-old Caucasian male with NT-AML M0 who had an unusually long first complete remission of 51 months and an overall survival of 80 months. The only characteristic distinguishing him from other previously described patients with NT-AML was the absence of erythroblastic and/or megakaryocytic dysplasia (EMD) at diagnosis. Molecular-genetic testing for AML fusion transcripts associated with a favorable prognosis (PML/RARα,AML1/ETO, and CBFβ/MYH11) were negative, as were other prognostic markers like MLL-PTD,FLT3-ITD, or mutations of FLT3-D835,NPM1, or CEBPA. Expression studies of ERG,MN1, and EVI1 revealed overexpression of ERG only. The absence of EMD may be a useful prognostic/diagnostic feature of this new rare subtype of NT-AML.
    PMID: 21701158 [PubMed - ...</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5019542</comments>
            <pubDate>Thu, 23 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5019542</guid>        </item>
        <item>
            <title>Successful Treatment of Amegakaryocytic Thrombocytopenia with Azathioprine.</title>
            <link>http://www.medworm.com/index.php?rid=5019541&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21701159%26dopt%3DAbstract</link>
            <description>We report a case of AAMT which was successfully treated with azathioprine 3 mg/kg/day. The clinical bleeding tendency resolved after treatment for 4 weeks and complete remission was documented after 6 weeks. Azathioprine treatment for AAMT is low risk, convenient, and cost-effective. Our successful experience suggests that azathioprine is potentially the treatment of choice after steroid failure.
    PMID: 21701159 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5019541</comments>
            <pubDate>Thu, 23 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5019541</guid>        </item>
        <item>
            <title>Hemochromatosis, HFE C282Y Homozygosity, and Polycystic Ovary Syndrome: Report of Two Cases and Possible Effects of Androgens and Hepcidin.</title>
            <link>http://www.medworm.com/index.php?rid=5019540&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21701160%26dopt%3DAbstract</link>
            <description>Authors: Barton JC, Barton JC
    No abstract available.
    PMID: 21701160 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5019540</comments>
            <pubDate>Thu, 23 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5019540</guid>        </item>
        <item>
            <title>Iron Chelation with Deferasirox in Two Patients with HFE Hemochromatosis and Chronic Anemia.</title>
            <link>http://www.medworm.com/index.php?rid=4924233&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21659727%26dopt%3DAbstract</link>
            <description>We present 2 patients with hyperferritinemia, increased liver iron and hemochromatosis-associated HFE genotypes. At diagnosis, both patients had chronic anemia that prevented initiation of phlebotomy. Iron chelation with deferasirox proved to be a safe and effective means of substantially lowering ferritin levels.
    PMID: 21659727 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4924233</comments>
            <pubDate>Thu, 09 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4924233</guid>        </item>
        <item>
            <title>Pure Red Cell Aplasia Induced Only by Intravenous Administration of Recombinant Human Erythropoietin.</title>
            <link>http://www.medworm.com/index.php?rid=4924240&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21654161%26dopt%3DAbstract</link>
            <description>We describe here the clinical course of one such rare patient with Ab-mediated PRCA. The patient was a 70-year-old man with chronic renal failure secondary to diabetic nephropathy. He had not received rhEPO therapy before the initiation of hemodialysis. He started hemodialysis and began to receive rhEPO therapy intravenously. Three months later, his hemoglobin level started declining and he became transfusion dependent. A diagnosis of Ab-mediated PRCA was made by bone marrow examination and detection of anti-EPO Abs. He was successfully treated with cyclosporine and became independent of blood transfusions. This case is a reminder that vigilance is required regarding the development of Ab-mediated PRCA upon rhEPO therapy, regardless of the administration route.
    PMID: 21654161 [PubMed -...</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4924240</comments>
            <pubDate>Mon, 06 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4924240</guid>        </item>
        <item>
            <title>Hypoplastic Myelodysplastic Syndrome Associated with der(1;7)(q10;p10) Presenting as Bone Marrow Failure.</title>
            <link>http://www.medworm.com/index.php?rid=4924252&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21646778%26dopt%3DAbstract</link>
            <description>Authors: Cho SY, Oh SH, Suh JT, Lee HJ, Lee WI, Baek SK, Cho KS, Park TS
    No abstract available.
    PMID: 21646778 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4924252</comments>
            <pubDate>Tue, 31 May 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4924252</guid>        </item>
        <item>
            <title>Paroxysmal Nocturnal Hemoglobinuria after Autologous Stem Cell Transplantation: Extinction of the Clone during Treatment with Eculizumab - Pathophysiological Implications of a Unique Clinical Case.</title>
            <link>http://www.medworm.com/index.php?rid=4877683&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21597283%26dopt%3DAbstract</link>
            <description>We report a previously undescribed case of PNH occurring after autologous stem cell transplantation (ASCT) in a patient affected by relapsing non-Hodgkin's lymphoma. The intensive chemotherapy and the ASCT resulted in a contraction of the effective hematopoietic stem cell (HSC) pool and a derangement of the immune system. The delayed engraftment and the BM hypoplasia represented a favorable environment for the expansion of the pathological clone. This case is paradigmatic even for the unexpected trend of the PNH clone during treatment with the terminal complement inhibitor eculizumab; in fact, the clone reduced until undergoing unexpected extinction, i.e. the recovery of normal hematopoiesis. Eculizumab seems not to play a direct role in HSC kinetics; the clinical remission probably occurr...</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4877683</comments>
            <pubDate>Wed, 18 May 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4877683</guid>        </item>
        <item>
            <title>Viability and Potency of Hematopoietic Progenitor Cells after Prolonged Cryopreservation at -80°C.</title>
            <link>http://www.medworm.com/index.php?rid=4877684&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21576935%26dopt%3DAbstract</link>
            <description>Authors: Costa R, Khattab M, Gilmore GL, Sahovic EA, Miller SM, Rossetti JM, Abdulhaq H, Lister J
    No abstract available.
    PMID: 21576935 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4877684</comments>
            <pubDate>Mon, 16 May 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4877684</guid>        </item>
        <item>
            <title>A Phytosterolemia Patient Presenting Exclusively with Macrothrombocytopenia and Stomatocytic Hemolysis.</title>
            <link>http://www.medworm.com/index.php?rid=4877685&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21576934%26dopt%3DAbstract</link>
            <description>Conclusion: We describe a phytosterolemia patient whose clinical manifestations were macrothrombocytopenia, stomatocytic hemolysis and splenomegaly, without the common features of this disorder. Our results suggest that blood cells could be a target for the toxic effect of plasma plant sterols, which should be measured in patients with unexplained stomatocytosis and/or macrothrombocytopenia in order to determine if they have phytosterolemia.
    PMID: 21576934 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4877685</comments>
            <pubDate>Wed, 11 May 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4877685</guid>        </item>
        <item>
            <title>Evidence for a Proatherogenic Biochemical Phenotype in Beta Thalassemia Minor and Intermedia.</title>
            <link>http://www.medworm.com/index.php?rid=4877686&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21576933%26dopt%3DAbstract</link>
            <description>Authors: Lai ME, Vacquer S, Carta MP, Spiga A, Cocco P, Abete C, Dessì S, Mandas A
    The purpose of this study was to focus on pathophysiological mechanisms linking β-thalassemia intermedia (β-TI) and minor (β-TMI) with cardiovascular risk. Iron status, prooxidant-antioxidant balance and lipid profiles in serum, and lipid content in peripheral blood mononuclear cells (PBMCs) were evaluated in 20 β-TMI subjects, 22 β-TI patients and in 30 nonthalassemic blood donors. The mRNA levels of some genes involved in the regulation of iron and cholesterol metabolism were also determined. In β-TI and in β-TMI, serum iron, prooxidant-antioxidant ratio, transferrin saturation and erythropoietin levels were higher, while transferrin and hepcidin were lower compared to controls. Hepcidin and in...</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4877686</comments>
            <pubDate>Tue, 10 May 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4877686</guid>        </item>
        <item>
            <title>Pretreatment Serum Level of 15-kDa Granulysin Might Have a Prognostic Value in Patients with Diffuse Large B Cell Lymphoma.</title>
            <link>http://www.medworm.com/index.php?rid=4824693&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21540579%26dopt%3DAbstract</link>
            <description>Conclusions: Pretreatment serum level of 15-kDa granulysin may be a valuable prognostic marker in DLBCL patients treated with standard chemotherapy.
    PMID: 21540579 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4824693</comments>
            <pubDate>Tue, 03 May 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4824693</guid>        </item>
        <item>
            <title>Therapy-Related Acute Myeloid Leukemia following Treatment with Trabectedin for Ewing's Sarcoma.</title>
            <link>http://www.medworm.com/index.php?rid=4824694&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21502754%26dopt%3DAbstract</link>
            <description>Authors: Liu SV, Zneimer S, Tahbaz A, Douer D
    No abstract available.
    PMID: 21502754 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4824694</comments>
            <pubDate>Sun, 17 Apr 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4824694</guid>        </item>
        <item>
            <title>Absence of Mutations on the SNF5 Gene in Hematological Neoplasms with Chromosome 22 Abnormalities.</title>
            <link>http://www.medworm.com/index.php?rid=4722113&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21494030%26dopt%3DAbstract</link>
            <description>Conclusion: These results suggest that alterations of the SNF5 gene are rare in hematological neoplasms with chromosome 22 abnormalities. Haploinsufficiency may contribute to the development of these neoplasms.
    PMID: 21494030 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4722113</comments>
            <pubDate>Tue, 12 Apr 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4722113</guid>        </item>
        <item>
            <title>Vitamin B(12)-Responsive Pancytopenia Mimicking Myelodysplastic Syndrome.</title>
            <link>http://www.medworm.com/index.php?rid=4722114&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21487214%26dopt%3DAbstract</link>
            <description>Authors: Heimpel H
    No abstract available.
    PMID: 21487214 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4722114</comments>
            <pubDate>Sun, 10 Apr 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4722114</guid>        </item>
        <item>
            <title>Proteolytic Matrix Metallopeptidases and Inhibitors in BCR-ABL1-Negative Myeloproliferative Neoplasms: Correlation with JAK2 Mutation Status.</title>
            <link>http://www.medworm.com/index.php?rid=4722118&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21474922%26dopt%3DAbstract</link>
            <description>Conclusions: Identification of an abnormal TIMP/MMP ratio in all three diseases, regardless of the JAK2 status, indicates invariable marrow remodeling. In this particular group of patients, presence of a JAK2(V617F) mutation, being associated with even higher ratios, appears to be a concurring participant in bone marrow-reforming processes. Additional research may delineate correlates with the JAK2 allelic burden.
    PMID: 21474922 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4722118</comments>
            <pubDate>Wed, 06 Apr 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4722118</guid>        </item>
        <item>
            <title>Disseminated Strongyloides stercoralis Infection in HTLV-1-Associated Adult T-Cell Leukemia/Lymphoma.</title>
            <link>http://www.medworm.com/index.php?rid=4722116&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21474923%26dopt%3DAbstract</link>
            <description>Authors: Stewart DM, Ramanathan R, Mahanty S, Fedorko DP, Janik JE, Morris JC
    A 55-year-old woman with human T-cell lymphotropic virus type-1 (HTLV-1)-associated adult T-cell leukemia (ATL) and a history of previously treated Strongyloides stercoralis infection received anti-CD52 monoclonal antibody therapy with alemtuzumab on a clinical trial. After an initial response, she developed ocular involvement by ATL. Alemtuzumab was stopped and high-dose corticosteroid therapy was started to palliate her ocular symptoms. Ten days later, the patient developed diarrhea, vomiting, fever, cough, skin rash, and a deteriorating mental status. She was diagnosed with disseminated S. stercoralis. Corticosteroids were discontinued and the patient received anthelmintic therapy with ivermectin and alben...</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4722116</comments>
            <pubDate>Wed, 06 Apr 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4722116</guid>        </item>
        <item>
            <title>Development of Polycythemia Vera after Chemotherapy-Induced Remission of Acute Myeloid Leukemia: A Case Report.</title>
            <link>http://www.medworm.com/index.php?rid=4669122&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21454967%26dopt%3DAbstract</link>
            <description>Authors: Belotti A, Doni E, Elli E, Rossi V, Pioltelli P, Pogliani EM
    No abstract available.
    PMID: 21454967 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4669122</comments>
            <pubDate>Wed, 30 Mar 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4669122</guid>        </item>
        <item>
            <title>High Ki67 Index and Bulky Disease Remain Significant Adverse Prognostic Factors in Patients with Diffuse Large B Cell Lymphoma before and after the Introduction of Rituximab.</title>
            <link>http://www.medworm.com/index.php?rid=4669161&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21430371%26dopt%3DAbstract</link>
            <description>Authors: Gaudio F, Giordano A, Perrone T, Pastore D, Curci P, Delia M, Napoli A, De' Risi C, Spina A, Ricco R, Liso V, Specchia G
    The aim of this study was to evaluate the impact of clinical variables and biologic features on response rate (RR), overall survival (OS) and progression-free survival (PFS) in 111 patients with de novo diffuse large B cell lymphoma (DLBCL). Fifty-three patients were treated with CHOP (cyclophosphamide, doxorubicin, vincristine and prednisolone) and 58 patients were treated with R-CHOP (rituximab + CHOP). The variables predictive of RR in the CHOP group were B symptoms, age, clinical stage, bone marrow involvement, bulky disease, International Prognostic Index (IPI) and Bcl-2; in the R-CHOP group, these variables were bulky disease, bone marrow involvement, ...</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4669161</comments>
            <pubDate>Thu, 24 Mar 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4669161</guid>        </item>
        <item>
            <title>Treatment of Synchronous Mantle Cell Lymphoma and Small Lymphocytic Lymphoma with Bendamustine and Rituximab.</title>
            <link>http://www.medworm.com/index.php?rid=4669162&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21430370%26dopt%3DAbstract</link>
            <description>Authors: Kourelis TV, Kahl BS, Benn P, Delach JA, Bilgrami SF
    Herein, we describe a case of a female patient in whom B cell chronic lymphocytic leukemia (CLL) and mantle cell lymphoma (MCL) were diagnosed simultaneously. She presented with anemia, thrombocytopenia and splenomegaly. Flow cytometry demonstrated two immunophenotypically distinct CD5-positive monoclonal B cell populations. Peripheral blood fluorescence in situ hybridization (FISH) was positive for IGH/CCND1, consistent with t(11;14) translocation. She received 6 cycles of bendamustine 70 mg/m(2)/day for 2 days and rituximab on the first day every 4 weeks along with granulocyte-colony stimulating factor. She had an excellent response, and repeat computed tomography after her third cycle of chemotherapy revealed no organomeg...</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4669162</comments>
            <pubDate>Wed, 23 Mar 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4669162</guid>        </item>
        <item>
            <title>Cyclosporine A for Chemotherapy-Resistant Subcutaneous Panniculitis-Like T Cell Lymphoma with Hemophagocytic Syndrome.</title>
            <link>http://www.medworm.com/index.php?rid=4609535&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21411984%26dopt%3DAbstract</link>
            <description>We report a case of chemotherapy-resistant SPTL with hemophagocytic syndrome (HPS) which was successfully treated with cyclosporine A (CsA) plus methylprednisolone (mPSL), and also reviewed 11 SPTL cases treated with CsA, previously reported in the literature. Our patient was a 38-year-old female with SPTL. The disease progressed despite conventional chemotherapy using cytotoxic agents including alkylators, anthracyclins or purine analogues, and, after 2 months of chemotherapy, was eventually complicated by HPS and disseminated intravascular coagulation (DIC). CsA (4 mg/kg/day) plus mPSL treatment dramatically improved HPS with DIC, reduced subcutaneous tumors within 2 weeks, and finally induced complete remission (CR) after 3 months. Currently, the patient has maintained CR while being tr...</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4609535</comments>
            <pubDate>Thu, 17 Mar 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4609535</guid>        </item>
        <item>
            <title>Expansion of CD56-Negative, CD16-Positive, KIR-Expressing Natural Killer Cells after T Cell-Depleted Haploidentical Hematopoietic Stem Cell Transplantation.</title>
            <link>http://www.medworm.com/index.php?rid=4609534&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21411985%26dopt%3DAbstract</link>
            <description>Authors: De Angelis C, Mancusi A, Ruggeri L, Capanni M, Urbani E, Velardi A, Stern M
    The main functions of natural killer (NK) cells are early protection against viruses or tumor cells and production of cytokines that regulate immune functions. The present study assessed the role of different NK subsets in exerting graft-versus-leukemia effects in recipients of human leukocyte antigen (HLA) haploidentical hematopoietic transplants and monitored for the first time CD3-/CD56- lymphocyte expansion. CD3-/CD56- cells expressed NK cell-associated molecules, such as CD16, NKp46, NKp30, CD244 (2B4), CD161, and killer cell immunoglobulin-like receptors. CD3-/CD56- cells further exhibited the classical functional characteristics of NK cells: cytolysis of target cells lacking HLA class I, antibod...</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4609534</comments>
            <pubDate>Thu, 17 Mar 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4609534</guid>        </item>
        <item>
            <title>Reduced-Intensity Conditioning Regimen Combined with Low-Dose Total Body Irradiation in the Treatment of Myelodysplastic Syndrome.</title>
            <link>http://www.medworm.com/index.php?rid=4609533&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21411986%26dopt%3DAbstract</link>
            <description>Authors: Lee SE, Lim J, Yahng SA, Cho BS, Eom KS, Kim M, Kim YJ, Kim HJ, Min CK, Lee S, Kim DW, Lee JW, Min WS, Park CW, Cho SG
    Although reduced-intensity conditioning (RIC) has been increasingly used in patients with myelodysplastic syndrome (MDS) to reduce transplant-related mortality, a high relapse rate in RIC remains an unresolved problem. Considering the additive antileukemic effect of low-dose total body irradiation (TBI), we evaluated the feasibility of combining RIC regimens with low-dose TBI in de novo MDS. The RIC regimen combined with low-dose TBI in this study consisted of fludarabine (150 mg/m(2)), intravenous busulfan (6.4 mg/kg), and TBI (400 cGy). Antithymocyte globulin was used to overcome HLA mismatching. A total of 31 subjects were recruited with a median age of 39 ...</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4609533</comments>
            <pubDate>Thu, 17 Mar 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4609533</guid>        </item>
        <item>
            <title>Challenges for Allogeneic Hematopoietic Stem Cell Transplantation in Chronic Myeloid Leukemia in the Era of Tyrosine Kinase Inhibitors.</title>
            <link>http://www.medworm.com/index.php?rid=4609532&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21411987%26dopt%3DAbstract</link>
            <description>Authors: Oyekunle A, Klyuchnikov E, Ocheni S, Kröger N, Zander AR, Baccarani M, Bacher U
    Following the introduction of the tyrosine kinase inhibitor (TKI) imatinib in the treatment of chronic myeloid leukemia (CML) patients, the allogeneic hematopoietic stem cell transplantation (HSCT) scene in CML has changed dramatically. The number of patients receiving HSCT in first chronic phase (CP) has declined rapidly, as allogeneic HSCT in CP is now performed in these patients only in case of failure or intolerance of TKIs. Second, those CML patients who undergo allogeneic HSCT represent a selection of high-risk patients due to more advanced disease with high rates of accelerated or blast phase (being associated with an increased relapse risk), advanced age and relevant co-morbidities. Effort...</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4609532</comments>
            <pubDate>Thu, 17 Mar 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4609532</guid>        </item>
        <item>
            <title>Management of the 2009 A/H1N1 Influenza Pandemic in Patients with Hematologic Diseases: A Prospective Experience at an Italian Center.</title>
            <link>http://www.medworm.com/index.php?rid=4609536&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21411983%26dopt%3DAbstract</link>
            <description>Authors: Girmenia C, Mercanti C, Federico V, Rea M, De Vellis A, Valle V, Micozzi A, Latagliata R, Breccia M, Morano SG, Brunetti GA, Sali M, Delogu G, Foà R, Alimena G, Gentile G
    Data derived from epidemiologic surveillance adopted at our center in hematologic and stem cell transplant patients during the 2009 influenza A (H1N1)v pandemic are reported. Of the 52 patients with influenza-like disease we observed, 37 underwent a real-time PCR evaluation and 21 had a confirmed diagnosis. Of the RT-PCR-confirmed cases, 23.8% were children (age &amp;lt;18 years) and 9.5% were &amp;gt;65 years; 47.6% presented with a pulmonary infiltrate and 33.3% with respiratory failure. Pulmonary involvement was observed more frequently in patients with comorbidities. All patients received a course of oseltamivir...</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4609536</comments>
            <pubDate>Fri, 11 Mar 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4609536</guid>        </item>
        <item>
            <title>p53 Protein Expression in Chronic Myelomonocytic Leukemia-1 Correlates with Progression to Leukemia and a Poor Prognosis.</title>
            <link>http://www.medworm.com/index.php?rid=4546354&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21335959%26dopt%3DAbstract</link>
            <description>Authors: Hattori N, Fukuchi K, Nakamaki T, Homma M, Ariizumi H, Nakashima H, Maeda T, Saito B, Yamochi-Onizuka T, Yanagisawa K, Matsuda I, Ota H, Tomoyasu S
    No abstract available.
    PMID: 21335959 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4546354</comments>
            <pubDate>Fri, 18 Feb 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4546354</guid>        </item>
        <item>
            <title>Herpesviridae Viral Infections following Rituximab Combined Chemotherapy in Patients with Diffuse Large B-Cell Lymphoma.</title>
            <link>http://www.medworm.com/index.php?rid=4490968&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21325812%26dopt%3DAbstract</link>
            <description>Conclusion: A high international prognostic index risk, neutropenic fever and a high cumulative dose of steroids appear to be risk factors for HVI in DLBL patients who are undergoing rituximab combined chemotherapy.
    PMID: 21325812 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4490968</comments>
            <pubDate>Sat, 12 Feb 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4490968</guid>        </item>
        <item>
            <title>Acute Myeloid Leukemia with a RUNX1-RUNX1T1 t(1;21;8)(q21;q22;q22) Novel Variant: A Case Report and Review of the Literature.</title>
            <link>http://www.medworm.com/index.php?rid=4490967&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21325813%26dopt%3DAbstract</link>
            <description>We report a 63-year-old female patient with AML, who showed a 3-way novel variant of t(8;21), t(1;21;8)(q21;q22;q22). She presented with gastric discomfort and splenomegaly, and her complete blood count was: white blood cell count 7.96 × 10(9)/l, with 7% blasts; hemoglobin 8.3 g/dl, and platelets 66 × 10(9)/l. Her bone marrow showed increased blasts (32.5%) with a basophilic cytoplasm, salmon-pink granules and Auer rods. Cytogenetic analysis revealed a karyotype of 46,XX,t(1;21;8)(q21;q22;q22), and fluorescence in situ hybridization confirmed a RUNX1-RUNX1T1 fusion signal on the derivative chromosome 8. After induction chemotherapy, the patient achieved complete remission and has been stable for 6 months. To the best of our knowledge, this is the first report on the novel variant of t(8;...</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4490967</comments>
            <pubDate>Sat, 12 Feb 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4490967</guid>        </item>
        <item>
            <title>An Elevated Estimated Pulmonary Arterial Systolic Pressure, Whenever Measured, Is Associated with Excess Mortality in Adults with Sickle Cell Disease.</title>
            <link>http://www.medworm.com/index.php?rid=4490969&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21282944%26dopt%3DAbstract</link>
            <description>Authors: Lorch D, Spevack D, Little J
    
    PMID: 21282944 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4490969</comments>
            <pubDate>Tue, 01 Feb 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4490969</guid>        </item>
        <item>
            <title>A Case of Well-Tolerated and Safe Deferasirox Administration during the First Trimester of a Spontaneous Pregnancy in an Advanced Maternal Age Thalassemic Patient.</title>
            <link>http://www.medworm.com/index.php?rid=4422613&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21273766%26dopt%3DAbstract</link>
            <description>In this report, we present a case of a spontaneous pregnancy in a 42-year-old thalassemic woman referred to our Microcythemic Unit while she was on deferasirox (DFX) therapy. The patient had been on treatment with DFX since March 2008 and in March 2009 realized that she was pregnant at 12 weeks of gestation. The conception was spontaneous and the baby was born at full term without complications or malformations.
    PMID: 21273766 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4422613</comments>
            <pubDate>Thu, 27 Jan 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4422613</guid>        </item>
        <item>
            <title>Clinical Characteristics, Biological Profile, and Outcome of Biphenotypic Acute Leukemia: A Case Series.</title>
            <link>http://www.medworm.com/index.php?rid=4422615&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21266800%26dopt%3DAbstract</link>
            <description>Conclusions: Our findings indicate that BAL shows a high incidence of abnormal karyotypes and a poor prognosis. Combined-type regimens or ALL-based protocols are effective for the treatment of BAL.
    PMID: 21266800 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4422615</comments>
            <pubDate>Tue, 25 Jan 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4422615</guid>        </item>
        <item>
            <title>Oral Iron Chelator Deferasirox in the Treatment of Secondary Hemochromatosis following Bone Marrow Transplantation in a Patient with Severe Aplastic Anemia.</title>
            <link>http://www.medworm.com/index.php?rid=4422614&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21266801%26dopt%3DAbstract</link>
            <description>Authors: Quarta A, Melpignano A, Quarta G
    Iron overload sometimes complicates the clinical course of bone marrow transplantation and can cause damage to liver and heart function. A patient with post-transplantation secondary hemochromatosis was treated with deferasirox, which not only normalized ferritin levels, but also reduced hepatic iron to normal values as measured by biosusceptometry with a superconducting quantum interference device. Side effects were minimal. The use of deferasirox to reduce post-transplant iron burden merits evaluation in a larger patient population.
    PMID: 21266801 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4422614</comments>
            <pubDate>Tue, 25 Jan 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4422614</guid>        </item>
        <item>
            <title>New Mutation in Erythroid-Specific Delta-Aminolevulinate Synthase as the Cause of X-Linked Sideroblastic Anemia Responsive to Pyridoxine.</title>
            <link>http://www.medworm.com/index.php?rid=4422620&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21252495%26dopt%3DAbstract</link>
            <description>Conclusion: Our report extends the list of known ALAS2 mutations, with the addition of a novel K156E substitution that is responsive to pyridoxine treatment and contributes to the general knowledge of congenital SA cases characterized worldwide.
    PMID: 21252495 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4422620</comments>
            <pubDate>Thu, 20 Jan 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4422620</guid>        </item>
        <item>
            <title>Vitamin B(12)-Responsive Pancytopenia Mimicking Myelodysplastic Syndrome.</title>
            <link>http://www.medworm.com/index.php?rid=4422618&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21252496%26dopt%3DAbstract</link>
            <description>This study presents 12 patients (7 women and 5 men) with vitamin B(12)-responsive pancytopenia who had discordant laboratory findings and were misdiagnosed as having myelodysplastic syndrome (MDS). The median hemoglobin level was 6.5 g/dl, and the leukocyte and platelet counts were 2.85 × 10(9)/l and 55.5 × 10(9)/l, respectively. The median serum lactate dehydrogenase level was high (3,204.5 IU/l). The serum vitamin B(12) levels were within normal limits at the initial evaluation, but a serial follow-up of the vitamin B(12) levels revealed either fluctuations or a gradual decrease. The patients were initially diagnosed with MDS and responded rapidly to a 7-day parenteral B(12) treatment with normal complete blood counts (CBCs). We propose that patients suspected to have MDS may suffer fr...</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4422618</comments>
            <pubDate>Thu, 20 Jan 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4422618</guid>        </item>
        <item>
            <title>E109K Is a SEC23B Founder Mutation among Israeli Moroccan Jewish Patients with Congenital Dyserythropoietic Anemia Type II.</title>
            <link>http://www.medworm.com/index.php?rid=4422617&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21252497%26dopt%3DAbstract</link>
            <description>Conclusions: Most CDA II patients in Israel are of Moroccan Jewish origin and carry a common SEC23B mutation, E109K, the first to be described as a founder mutation causing CDA II. As previously suggested, carrying 2 missense mutations is associated with a relatively nonsevere phenotype.
    PMID: 21252497 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4422617</comments>
            <pubDate>Thu, 20 Jan 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4422617</guid>        </item>
        <item>
            <title>Mean Platelet Volume as a Marker of Thrombosis in Patients with Missed Abortion.</title>
            <link>http://www.medworm.com/index.php?rid=4422616&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21252498%26dopt%3DAbstract</link>
            <description>Authors: Kosus N, Kosus A, Yıldırım M, Duran M, Turhan NO
    No abstract available.
    PMID: 21252498 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4422616</comments>
            <pubDate>Thu, 20 Jan 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4422616</guid>        </item>
        <item>
            <title>Anemia, Iron Deficiency and Thalassemia among Adolescents in Northeast Thailand: Results from Two Independent Surveys.</title>
            <link>http://www.medworm.com/index.php?rid=4359297&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21228565%26dopt%3DAbstract</link>
            <description>Authors: Pansuwan A, Fucharoen G, Fucharoen S, Himakhun B, Dangwiboon S
    The prevalence of adolescent anemia, iron deficiency and thalassemia were examined in 2 provinces of northeast Thailand. Blood specimens were collected from adolescent subjects aged 15-17 years in 2 areas; 185 (85 males and 100 females) in Mukdahan province and 313 (116 males and 197 females) in Roi-Et. RBC parameters, serum ferritin levels, Hb and DNA analyses for the identification of common thalassemia genes in Thailand were investigated. The prevalences of anemia were found to be 21.1% (8.1 in male and 13.0 in female) and 16.6% (8.9 in male and 7.7 in female) in Mukdahan and Roi-Et province, respectively. Iron deficiency was observed to be 24.3% in Mukdahan and 14.7% in Roi-Et. Various types of thalassemia were...</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4359297</comments>
            <pubDate>Thu, 13 Jan 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4359297</guid>        </item>
        <item>
            <title>Aberrant Methylation of Death-Associated Protein Kinase 1 CpG Islands in Myelodysplastic Syndromes.</title>
            <link>http://www.medworm.com/index.php?rid=4359298&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21212658%26dopt%3DAbstract</link>
            <description>Authors: Wu X, Liu W, Tian Y, Xiao M, Wu Y, Li C
    Death-associated protein kinase 1 (DAPK1), a proapoptotic serine/threonine kinase, is a candidate tumor suppressor gene. We studied the methylation status of the promoter region of the DAPK1 gene and the expression of the DAPK1 protein in 78 bone marrow samples from untreated patients with myelodysplastic syndrome (MDS) by PCR and Western blot analysis. Hypermethylation of DAPK1 was present in 42.3% (33 of 78) of MDS specimens and was significantly correlated with the loss of DAPK1 mRNA and protein expression (p &amp;lt; 0.01). There were no significant differences in methylation frequency among subgroup of MDS. DAPK1 hypermethylation in MDS was associated with the presence of cytogenetic abnormalities in the bone marrow at the time of the i...</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4359298</comments>
            <pubDate>Tue, 04 Jan 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4359298</guid>        </item>
        <item>
            <title>Castleman's Disease Presenting as Prolonged Anemia and Growth Retardation: A Case Report and Literature Review.</title>
            <link>http://www.medworm.com/index.php?rid=4259976&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21150179%26dopt%3DAbstract</link>
            <description>Authors: Yang M, Wang FD, Han B, Wang SJ, Zhou DB, Pan H, Zhao YQ, Cui QC, Ma L, Chng WJ, Shen T
    No abstract available.
    PMID: 21150179 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4259976</comments>
            <pubDate>Wed, 15 Dec 2010 17:01:16 +0100</pubDate>
            <guid isPermaLink="false">4259976</guid>        </item>
        <item>
            <title>Introduction.</title>
            <link>http://www.medworm.com/index.php?rid=4259968&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21150182%26dopt%3DAbstract</link>
            <description>Authors: Raanani P, Skoetz N
    No abstract available.
    PMID: 21150182 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4259968</comments>
            <pubDate>Wed, 15 Dec 2010 17:00:31 +0100</pubDate>
            <guid isPermaLink="false">4259968</guid>        </item>
        <item>
            <title>Treatment of Patients with Multiple Myeloma: An Overview of Systematic Reviews.</title>
            <link>http://www.medworm.com/index.php?rid=4259963&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21150183%26dopt%3DAbstract</link>
            <description>The objective of this overview is to summarize all existing systematic reviews on treatments in multiple myeloma (MM), which accounts for 14% of new cases of hematological malignancies each year. Therefore, MEDLINE and the Cochrane Database of Systematic Reviews were systematically searched to identify systematic reviews of interventions. Data were extracted on patients, interventions, control and outcomes. Methodological quality of the systematic reviews was assessed using the AMSTAR assessment tool. Eleven systematic reviews on treatment of MM were included in the overview. Ten addressed seven unique questions and also performed a meta-analysis. One addressed 21 clinical questions related to treatment decisions in myeloma. The quality of systematic reviews varied. The results from the ov...</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4259963</comments>
            <pubDate>Wed, 15 Dec 2010 17:00:12 +0100</pubDate>
            <guid isPermaLink="false">4259963</guid>        </item>
        <item>
            <title>Immunotherapy for Patients with Follicular Lymphoma: The Contribution of Systematic Reviews.</title>
            <link>http://www.medworm.com/index.php?rid=4259953&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21150184%26dopt%3DAbstract</link>
            <description>Authors: Vidal L, Gafter-Gvili A, Shpilberg O
    The course of follicular lymphoma has changed considerably with the introduction of immunotherapy. Systematic reviews and meta-analyses are reliable, efficient and well-established methods to summarize the vast amount of data acquired in recent years on the role of immunotherapy, including monoclonal antibodies, radio-labeled monoclonal antibodies and interferon-α in the treatment of patients with follicular lymphoma. We aimed to summarize the data from systematic reviews assessing immunotherapy for these patients. A search through Medline and the Cochrane Library for systematic reviews of randomized controlled trials of different types of immunotherapy for patients with follicular lymphoma yielded 17 reviews. Eleven of them were eligible ...</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4259953</comments>
            <pubDate>Wed, 15 Dec 2010 16:59:44 +0100</pubDate>
            <guid isPermaLink="false">4259953</guid>        </item>
        <item>
            <title>Meta-Analyses of Early-Stage Hodgkin Lymphoma.</title>
            <link>http://www.medworm.com/index.php?rid=4259913&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21150185%26dopt%3DAbstract</link>
            <description>Authors: Herbst C, Engert A
    Meta-analyses have followed some of the most important advances in the treatment of early-stage Hodgkin lymphoma (HL). In this review, details on all meta-analyses of patients with early-stage HL are discussed. In 1990, the first meta-analysis addressing patients with early-stage HL compared radiotherapy alone to combined-modality treatment (CMT). It was followed in 1998 by an individual-patient meta-analysis examining the role of radiotherapy with and without chemotherapy. In 2006, a comprehensive meta-analysis focusing on the risk of secondary malignancies, including most of the treatment regimens analyzed in clinical trials, was issued. The final analysis was published 2010 and provides important information for the ongoing discussion concerning the role ...</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4259913</comments>
            <pubDate>Wed, 15 Dec 2010 16:59:05 +0100</pubDate>
            <guid isPermaLink="false">4259913</guid>        </item>
        <item>
            <title>Allogeneic Hematopoietic Cell Transplantation for Adult Patients with Acute Leukemia: The Role of Meta-Analyses.</title>
            <link>http://www.medworm.com/index.php?rid=4259894&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21150186%26dopt%3DAbstract</link>
            <description>Authors: Ram R, Gafter-Gvili A, Shpilberg O, Raanani P
    In spite of decades of research in the field of allogeneic hematopoietic cell transplantation for the treatment of acute leukemia, controversies regarding the role of transplant still exist. These stem not only from contradictory results of different studies, but also from differences in the design and the strength of evidence of the various trials. Meta-analysis is considered the highest level of evidence and as such has the power to resolve clinical issues comparing between different treatment modalities. The aim of this review is to examine the contribution of meta-analyses to the establishment of the role of hematopoietic transplantation for acute leukemia and at the same time to highlight limitations and future directions.
   ...</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4259894</comments>
            <pubDate>Wed, 15 Dec 2010 16:58:21 +0100</pubDate>
            <guid isPermaLink="false">4259894</guid>        </item>
        <item>
            <title>Management of Aplastic Anemia: The Role of Systematic Reviews and Meta-Analyses.</title>
            <link>http://www.medworm.com/index.php?rid=4259864&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21150187%26dopt%3DAbstract</link>
            <description>The objective of this review is to assess the base of evidence for the common practice and the current guidelines for the management of aplastic anemia. It focuses on data obtained from systematic reviews and meta-analyses of RCTs conducted in this field. Specifically, it focuses on four major therapeutic questions: the roles of alloHCT, IST, hematopoietic growth factors and supportive care.
    PMID: 21150187 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4259864</comments>
            <pubDate>Wed, 15 Dec 2010 16:56:25 +0100</pubDate>
            <guid isPermaLink="false">4259864</guid>        </item>
        <item>
            <title>Twist and Shout: One Decade of Meta-Analyses of Erythropoiesis-Stimulating Agents in Cancer Patients.</title>
            <link>http://www.medworm.com/index.php?rid=4259842&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21150188%26dopt%3DAbstract</link>
            <description>Authors: Bohlius J, Tonia T, Schwarzer G
    Anemia associated with cancer and cancer therapy is a common and important issue in the treatment of patients with malignant disease. Conventionally, blood transfusions are used to treat severe cancer-related anemia. Short- and long-acting preparations of recombinant human erythropoiesis-stimulating agents (ESAs) offer an alternative treatment option. Multiple studies and subsequent meta-analyses have demonstrated that ESA treatment increases hemoglobin levels and reduces the likelihood of transfusion for a proportion of treated patients. However, studies that attempted to evaluate whether ESAs improve tumor response and survival have generated conflicting evidence. Results of smaller trials reporting improved survival outcomes were contradicted...</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4259842</comments>
            <pubDate>Wed, 15 Dec 2010 16:53:22 +0100</pubDate>
            <guid isPermaLink="false">4259842</guid>        </item>
        <item>
            <title>The Use of Myeloid Colony-Stimulating Factors in Hematologic Malignancies: The Role of Systematic Reviews and Meta-Analyses.</title>
            <link>http://www.medworm.com/index.php?rid=4259765&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21150189%26dopt%3DAbstract</link>
            <description>Authors: Gurion R, Shacham-Abulafia A, Shpilberg O, Raanani P
    Myeloid colony-stimulating factors (M-CSFs), which include granulocyte colony-stimulating factor (G-CSF) and granulocyte-macrophage colony-stimulating factor (GM-CSF), regulate the proliferation and differentiation of myeloid cells. Their use has an important role in the treatment of hematologic malignancies. Guidelines for the use of colony stimulating factors have been published by the American Society of Oncology (ASCO) in 1996 and have been updated several times, most recently in 2006. Meta-analyses of randomized controlled trials are regarded as the highest grade of evidence in clinical research and as such, compared to individual studies, they have more power in answering unresolved clinical issues. In this review, our...</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4259765</comments>
            <pubDate>Wed, 15 Dec 2010 15:58:57 +0100</pubDate>
            <guid isPermaLink="false">4259765</guid>        </item>
        <item>
            <title>Infections in Hematogical Cancer Patients: The Contribution of Systematic Reviews and Meta-Analyses.</title>
            <link>http://www.medworm.com/index.php?rid=4259725&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21150190%26dopt%3DAbstract</link>
            <description>Authors: Paul M, Gafter-Gvili A, Goldberg E, Yahav D
    Systematic reviews and meta-analyses have made a major contribution to the evidence-based management of infections in cancer patients. We review the contribution of systematic reviews with regard to antibiotic, antifungal, antiviral and Pneumocystis pneumonia prophylaxis; antibiotic and antifungal treatment of febrile neutropenia; use of intravenous immunoglobulins, and infection control strategies during neutropenia. We focus on limitations of randomized controlled trials and the way systematic reviews have addressed and resolved some of these limitations. Systematic reviews allow us to ask the right clinical question; consider the most relevant clinical outcome; address the problem of small trials and rare outcomes; address externa...</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4259725</comments>
            <pubDate>Wed, 15 Dec 2010 14:49:57 +0100</pubDate>
            <guid isPermaLink="false">4259725</guid>        </item>
        <item>
            <title>How Helpful Are Meta-Analyses in Determining the Best Therapy of Blood Diseases?</title>
            <link>http://www.medworm.com/index.php?rid=4259682&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21150191%26dopt%3DAbstract</link>
            <description>Authors: Gale RP, Lazarus HM
    Meta-analyses of data from randomized clinical trials (RCTs) are often used by hematologists to compare the efficacy of therapies of blood diseases. This is especially so when results of RCTs are not decisive. This situation in RCTs arises when the magnitude of differences in treatment outcomes between therapies tested is small, when trials are unpowered to detect differences (these are confounded) and/or when RCTs reach, or seem to reach, contradictory conclusions. Contributing to these limitations of RCTs are the relative rarity of many blood diseases, poor recruitment into RCTs and the greater interest of many hematologists in therapy strategy than in a direct comparison of alternate therapies. These limitations of RCTs are solvable, but only in part, by...</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4259682</comments>
            <pubDate>Wed, 15 Dec 2010 13:57:06 +0100</pubDate>
            <guid isPermaLink="false">4259682</guid>        </item>
        <item>
            <title>Thrombomodulin and von Willebrand Factor: Relation to Endothelial Dysfunction and Disease Outcome in Children with Acute Lymphoblastic Leukemia.</title>
            <link>http://www.medworm.com/index.php?rid=4259973&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21150180%26dopt%3DAbstract</link>
            <description>In conclusion, severe endothelial dysfunction is present during the acute phase of ALL and during treatment and appears to result from the disease itself. Serum TM and vWF levels might represent additional, but not independent, prognostic markers in childhood ALL.
    PMID: 21150180 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4259973</comments>
            <pubDate>Sat, 11 Dec 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4259973</guid>        </item>
        <item>
            <title>Reliability of EMA Binding Test in the Diagnosis of Hereditary Spherocytosis in Italian Patients.</title>
            <link>http://www.medworm.com/index.php?rid=4259970&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21150181%26dopt%3DAbstract</link>
            <description>Authors: D'Alcamo E, Agrigento V, Sclafani S, Vitrano A, Cuccia L, Maggio A, Perrotta S, Capra M, Rigano P
    No abstract available.
    PMID: 21150181 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4259970</comments>
            <pubDate>Sat, 11 Dec 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4259970</guid>        </item>
        <item>
            <title>Hepatitis B Virus Reactivation in a Primary Central Nervous System Lymphoma Patient following Intrathecal Rituximab Treatment.</title>
            <link>http://www.medworm.com/index.php?rid=4259978&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21150178%26dopt%3DAbstract</link>
            <description>Authors: Kim MG, Park SY, Kim EJ, Kim YM, Kim HY, Lee YK, Zang DY, Kim HJ
    A 69-year-old woman with relapsed primary central nervous system (CNS) lymphoma was treated with intrathecal rituximab without a concomitant systemic steroid or other chemotherapeutic drugs. Her initial viral status was HBs Ag negative and anti-HBs Ab positive. After 12 weeks of the last intrathecal rituximab application, the levels of AST and ALT were 1,005 and 1,134 IU/l, respectively. The viral status was changed as follows: HBs Ag positive, anti-HBs Ab negative, anti-HBe Ag positive, and anti-HBe Ab negative. The titer of hepatitis B virus (HBV) DNA was 106,000 IU/ml. She was diagnosed with acute hepatitis due to HBV reactivation. To our knowledge, this is the first reported case of HBV reactivation occurring...</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4259978</comments>
            <pubDate>Wed, 08 Dec 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4259978</guid>        </item>
        <item>
            <title>The Status of Thrombophilic Defects and Non-O Blood Group as Risk Factors for Gestational Vascular Complications among Tunisian Women.</title>
            <link>http://www.medworm.com/index.php?rid=4205685&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21109732%26dopt%3DAbstract</link>
            <description>Conclusion: Our results provide evidence for a significant association between the factor V mutation and placental abruption. Furthermore, we found that this and the non-O blood group independently increased the risk for intra-uterine growth retardation in our population.
    PMID: 21109732 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4205685</comments>
            <pubDate>Sat, 27 Nov 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4205685</guid>        </item>
        <item>
            <title>Breakthrough Febrile Neutropenia and Associated Complications in Non-Hodgkin's Lymphoma Patients Receiving Pegfilgrastim.</title>
            <link>http://www.medworm.com/index.php?rid=4205686&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21109731%26dopt%3DAbstract</link>
            <description>Conclusion: Despite routine administration of pegfilgrastim with CHOP chemotherapy, a high proportion of patients experienced FN after chemotherapy. Identifying patients at risk for breakthrough FN events may allow the optimization of myeloid growth factor usage among lymphoma patients receiving chemotherapy.
    PMID: 21109731 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4205686</comments>
            <pubDate>Thu, 25 Nov 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4205686</guid>        </item>
        <item>
            <title>Plasma Glial Fibrillary Acidic Protein Levels in a Child with Sickle Cell Disease and Stroke.</title>
            <link>http://www.medworm.com/index.php?rid=4205687&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21099215%26dopt%3DAbstract</link>
            <description>Authors: Savage WJ, Everett AD, Casella JF
    A 12-year-old boy with HbSS sickle cell disease (SCD) was admitted with an acute febrile illness and developed overt stroke 3 days later. Plasma glial fibrillary acidic protein levels were elevated, as compared to pediatric controls, 32 h prior to the clinical diagnosis of stroke, peaked immediately prior to the exchange transfusion, and remained elevated 1 year later despite chronic transfusion therapy. Stroke in SCD can occur in the setting of acute illness, and a biomarker that could predict the onset and triage ill children to therapeutic intervention more quickly would be useful.
    PMID: 21099215 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4205687</comments>
            <pubDate>Wed, 24 Nov 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4205687</guid>        </item>
        <item>
            <title>Ox Brain versus Rabbit Brain Thromboplastin Assays Are the Best Tool for a Preliminary Diagnosis of the Arg304Gln Factor VII Defect (FVII Padua).</title>
            <link>http://www.medworm.com/index.php?rid=4205691&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21099211%26dopt%3DAbstract</link>
            <description>Authors: Girolami A, Berti de Marinis G, Bonamigo E, Sartori R, Vettore S
    Factor VII (FVII) deficiency, the most frequent defect among the rare bleeding disorders, is commonly divided into type I and type II. In the former, there is a concomitant decrease in FVII activity and antigen. In the latter, there is a clear discrepancy between activity which is low and antigen which is normal or nearly normal. FVII Padua (Arg304Gln) is characterized by different reactivity towards different tissue thromboplastins. FVII levels were assayed by the use of different tissue thromboplastins, namely rabbit brain, human placenta, human recombinant and ox brain thromboplastin, in 6 homozygous patients. Cases reported in the literature were also evaluated. Ox brain thromboplastins yielded normal values,...</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4205691</comments>
            <pubDate>Sat, 20 Nov 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4205691</guid>        </item>
        <item>
            <title>Plerixafor Enables Successful Hematopoietic Stem Cell Collection in an Extensively Pretreated Patient with Testicular Cancer.</title>
            <link>http://www.medworm.com/index.php?rid=4205690&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21099212%26dopt%3DAbstract</link>
            <description>We report the case of a 26-year-old man with testicular cancer who was extensively pretreated and failed to mobilize a sufficient number of HPSCs after cytotoxic chemotherapy and the administration of G-CSF and pegylated G-CSF (PEG-G-CSF). Using a combination of plerixafor, G-CSF and PEG-G-GSF after chemotherapy, a sufficient number of HPSCs could be collected for the support of 3 sequential high-dose therapies. The patient achieved a complete and uncomplicated engraftment following each cycle of HPSC-supported high-dose therapy. Patients suffering from advanced germ cell cancer may be another group that benefits from the use of plerixafor, which to date has only been approved for the treatment of multiple myeloma and lymphoma. To our knowledge, this is the first case report of successful ...</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4205690</comments>
            <pubDate>Sat, 20 Nov 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4205690</guid>        </item>
        <item>
            <title>The Significance of Bone Marrow Involvement in Aggressive Lymphomas: A Retrospective Comparison of Clinical Outcomes between Peripheral T Cell Lymphoma and Diffuse Large B Cell Lymphoma in China.</title>
            <link>http://www.medworm.com/index.php?rid=4205689&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21099213%26dopt%3DAbstract</link>
            <description>Conclusions: PTCL with BMI have a similar aggressive course and poor survival compared to DLBCL with BMI. Thus, the immunophenotype of either T or B lineage may not be a crucial prognostic indicator of survival for these 2 aggressive lymphomas.
    PMID: 21099213 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4205689</comments>
            <pubDate>Sat, 20 Nov 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4205689</guid>        </item>
        <item>
            <title>The Use of Anti-Human T Lymphocyte Porcine Immunoglobulin and Cyclosporine A to Treat Patients with Acquired Severe Aplastic Anemia.</title>
            <link>http://www.medworm.com/index.php?rid=4205688&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21099214%26dopt%3DAbstract</link>
            <description>Conclusion: p-ALG plus CsA is a reliable and well-tolerated treatment for SAA, and it has the great advantage of a much lower cost compared to horse/rabbit ATG. VSAA was a poor predictive factor for the response rate.
    PMID: 21099214 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4205688</comments>
            <pubDate>Sat, 20 Nov 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4205688</guid>        </item>
        <item>
            <title>In vivo Evaluation Method of the Effect of Nattokinase on Carrageenan-Induced Tail Thrombosis in a Rat Model.</title>
            <link>http://www.medworm.com/index.php?rid=4173367&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21071931%26dopt%3DAbstract</link>
            <description>Authors: Kamiya S, Hagimori M, Ogasawara M, Arakawa M
    Thrombosis is characterized by congenital and acquired procatarxis. Nattokinase inhibits thrombus formation in vitro. However, in vivo evaluation of the therapeutic efficacy of nattokinase against thrombosis remains to be conducted. Subcutaneous nattokinase injections of 1 or 2 mg/ml were administered to the tails of rats. Subsequently, κ-carrageenan was intravenously administered to the tails at 12 h after nattokinase injections. The mean length of the infarcted regions in the tails of rats was significantly shorter in rats administered 2 mg/ml of nattokinase than those in control rats. Nattokinase exhibited significant prophylactic antithrombotic effects. Previously, the in vitro efficacy of nattokinase against thrombosis had bee...</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4173367</comments>
            <pubDate>Sat, 13 Nov 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4173367</guid>        </item>
        <item>
            <title>Spontaneous Regression of Chronic Myeloid Leukemia during Pregnancy.</title>
            <link>http://www.medworm.com/index.php?rid=4173366&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21071932%26dopt%3DAbstract</link>
            <description>Authors: Bernardeschi P, Pirrotta MT
    No abstract available.
    PMID: 21071932 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4173366</comments>
            <pubDate>Sat, 13 Nov 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4173366</guid>        </item>
        <item>
            <title>HJV Hemochromatosis, Iron Overload, and Hypogonadism in a Brazilian Man: Treatment with Phlebotomy and Deferasirox.</title>
            <link>http://www.medworm.com/index.php?rid=4173370&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21071928%26dopt%3DAbstract</link>
            <description>Authors: Santos PC, Cançado RD, Pereira AC, Chiattone CS, Krieger JE, Guerra-Shinohara EM
    No abstract available.
    PMID: 21071928 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4173370</comments>
            <pubDate>Fri, 12 Nov 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4173370</guid>        </item>
        <item>
            <title>Acute Myelogenous Leukemia Patients Are at Low Risk for Invasive Fungal Infections after High-Dose Cytarabine Consolidations and Thus Do Not Require Prophylaxis.</title>
            <link>http://www.medworm.com/index.php?rid=4173369&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21071929%26dopt%3DAbstract</link>
            <description>Authors: Lewis G, Hall P, Eisa N, Deremer D, Dobbins R, El-Geneidy M, Jillella A, Ustun C
    We evaluated the frequency of invasive fungal infections (IFI), the frequency of empirical antifungal use (EAFU), and the efficacy of fluconazole prophylaxis on IFI and EAFU after high-dose cytarabine (HiDAC) consolidations. Twenty-seven acute myelogenous leukemia patients in their first complete remission received 76 cycles of HiDAC (median cycle: n = 3). Fluconazole prophylaxis was administered following 44 cycles (fluconazole group) and not given in 32 cycles (control group). IFI (2 episodes) + EAFU (11 episodes) was observed in 13 of 76 cycles (17%); there was no difference between the fluconazole group and the control group (p = 0.469). Neutropenia duration was &amp;lt;13 days in 89% of the 76 cy...</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4173369</comments>
            <pubDate>Fri, 12 Nov 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4173369</guid>        </item>
        <item>
            <title>High Factor VIII Activity, High Plasminogen Activator Inhibitor 1 Antigen Levels and Low Factor XII Activity Contribute to a Thrombophilic Tendency in Elderly Venous Thromboembolism Patients.</title>
            <link>http://www.medworm.com/index.php?rid=4173368&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21071930%26dopt%3DAbstract</link>
            <description>Authors: Gary T, Hafner F, Froehlich H, Stojakovic T, Scharnagl H, Pilger E, Brodmann M
    No abstract available.
    PMID: 21071930 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4173368</comments>
            <pubDate>Fri, 12 Nov 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4173368</guid>        </item>
        <item>
            <title>Serum Adipocytokine and Vascular Inflammation Marker Levels in Beta-Thalassaemia Major Patients.</title>
            <link>http://www.medworm.com/index.php?rid=4125991&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21042009%26dopt%3DAbstract</link>
            <description>Conclusions: Serum leptin is low in beta-thalassaemia, perhaps due to the toxic effect of iron overload on adipose tissue. Paradoxically, adiponectin levels are high and positively correlated with endothelin-1, raising questions about the pro- or anti-inflammatory role of this adipocytokine in beta-thalassaemia.
    PMID: 21042009 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4125991</comments>
            <pubDate>Tue, 02 Nov 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4125991</guid>        </item>
        <item>
            <title>A Severe Case of Cefoxitin-Induced Immune Hemolytic Anemia.</title>
            <link>http://www.medworm.com/index.php?rid=4125990&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21042010%26dopt%3DAbstract</link>
            <description>We report a case of severe hemolytic anemia induced by cefoxitin in a 45-year-old woman admitted with menometrorrhagia. Hemoglobin levels reached a nadir of 4.7 g/dl approximately 72 h after cefoxitin initiation, and hemolysis resolved when cefoxitin was discontinued and prednisone 1 mg/kg was initiated. A transfusion reaction workup revealed no abnormalities. Direct antiglobulin testing was weakly positive with anti-C3. The patient's plasma and RBC eluate reacted with cefoxitin-treated RBCs but not with untreated RBCs in the presence or absence of cefoxitin.
    PMID: 21042010 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4125990</comments>
            <pubDate>Tue, 02 Nov 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4125990</guid>        </item>
        <item>
            <title>Reduced-Intensity Conditioning Using Fludarabine and Antithymocyte Globulin Alone Allows Stable Engraftment in a Patient with Dyskeratosis Congenita.</title>
            <link>http://www.medworm.com/index.php?rid=4125989&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21042011%26dopt%3DAbstract</link>
            <description>We describe the successful treatment of a 21-year-old male with DC by nonmyeloablative HSCT from a matched unrelated donor. The gene responsible for the X-linked form of DC was screened and hemizygosity for the mutation Gln31Lys was found, which is consistent with the diagnosis. The conditioning regimen consisted of only fludarabine and antithymocyte globulin. Additionally, a graft-versus-host disease (GVHD) prophylaxis was administered with cyclosporine A (CSA) and mycophenolate mofetil (MMF). The regimen was well tolerated, no severe posttransplantation complications were observed, and engraftment was rapid and complete (granulocytes on day +11 and platelets on day +13). Seven months after HSCT, the patient developed GVHD of the liver after tapering CSA which was successfully treated wit...</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4125989</comments>
            <pubDate>Tue, 02 Nov 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4125989</guid>        </item>
        <item>
            <title>Reversible Painful Oral Mucosal Hyperpigmentation following Palifermin Administration.</title>
            <link>http://www.medworm.com/index.php?rid=4098883&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20962520%26dopt%3DAbstract</link>
            <description>Authors: Kaloyannidis P, Papalexandri A, Papaemanouil E, Papaioannou M, Sakellari I
    No abstract available.
    PMID: 20962520 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4098883</comments>
            <pubDate>Wed, 20 Oct 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4098883</guid>        </item>
        <item>
            <title>der(14)t(6;14)(p21;q32) Detected in a Phytohemagglutinin-Stimulated Culture from an Asymptomatic Woman with CD5 Monoclonal B-Cell Lymphocytosis.</title>
            <link>http://www.medworm.com/index.php?rid=4098882&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20962521%26dopt%3DAbstract</link>
            <description>Authors: Romo Martinez EJ, Vasquez Jimenez EA, Barajas Torres RL, Delgado Lamas JL, Magaña Torres MT, Gonzalez Garcia JR
    No abstract available.
    PMID: 20962521 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4098882</comments>
            <pubDate>Wed, 20 Oct 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4098882</guid>        </item>
        <item>
            <title>Leukocyte Alkaline Phosphatase Score Correlation with Bone Marrow Blast Percentage in Myelodysplastic Syndrome.</title>
            <link>http://www.medworm.com/index.php?rid=4098885&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20962518%26dopt%3DAbstract</link>
            <description>Authors: Lipshitz J, Limaye S, Patel D
    No abstract available.
    PMID: 20962518 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4098885</comments>
            <pubDate>Tue, 19 Oct 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4098885</guid>        </item>
        <item>
            <title>Increased Risk for Acute Lymphoblastic Leukemia in Children with Cytochrome P(450) A(1)(CYP1A1)- and NAD(P)H:Quinone Oxidoreductase 1 (NQO1)-Inherited Gene Variants.</title>
            <link>http://www.medworm.com/index.php?rid=4098884&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20962519%26dopt%3DAbstract</link>
            <description>Authors: Yamaguti GG, Lourenço GJ, Silveira VS, Tone LG, Lopes LF, Lima CS
    No abstract available.
    PMID: 20962519 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4098884</comments>
            <pubDate>Tue, 19 Oct 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4098884</guid>        </item>
        <item>
            <title>An Unusual Case of Ankylosing Spondylitis Presenting with Severe Anemia.</title>
            <link>http://www.medworm.com/index.php?rid=4098886&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20948190%26dopt%3DAbstract</link>
            <description>Authors: Tadmor T, Rimar D, Rozenbaum M, Vadasz Z, Attias D
    No abstract available.
    PMID: 20948190 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4098886</comments>
            <pubDate>Thu, 14 Oct 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4098886</guid>        </item>
        <item>
            <title>Prevalence of the JAK2 V617F and MPL Mutations in Stroke, Abdominal and Peripheral Venous Thrombosis.</title>
            <link>http://www.medworm.com/index.php?rid=4067101&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20938171%26dopt%3DAbstract</link>
            <description>Authors: McCarthy N, McCarron SL, Langabeer SE
    No abstract available.
    PMID: 20938171 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4067101</comments>
            <pubDate>Tue, 12 Oct 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4067101</guid>        </item>
        <item>
            <title>Serum Cytokine Profiles at the Onset of Severe, Diffuse Alveolar Hemorrhage Complicating Allogeneic Hematopoietic Stem Cell Transplantation, Treated Successfully with Pulse Intravenous Cyclophosphamide.</title>
            <link>http://www.medworm.com/index.php?rid=4067099&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20938173%26dopt%3DAbstract</link>
            <description>Authors: Koh H, Nakamae H, Koh KR, Ohsawa M, Nakane T, Takeoka Y, Aimoto R, Aimoto M, Wada-Inoue E, Terada Y, Yamane T, Hino M
    A 59-year-old man with lymphoma-type adult T-cell leukemia/lymphoma was admitted to hospital for treatment of a skin relapse on day 398 after allogeneic hematopoietic stem cell transplantation (allo-HSCT). To induce a graft-versus-adult T-cell leukemia/lymphoma effect, we discontinued methylprednisolone and tacrolimus. About a month after the discontinuation, he developed grade II acute graft-versus-host disease (GVHD) with a high fever. Soon after the development of GVHD, all the skin lesions regressed in size and finally vanished. However, he developed diffuse alveolar hemorrhage (DAH), which was resistant to high-dose corticosteroid therapy. He was intubated...</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4067099</comments>
            <pubDate>Tue, 12 Oct 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4067099</guid>        </item>
        <item>
            <title>β-Globin Gene Cluster Haplotypes in a Cohort of 221 Children with Sickle Cell Anemia or Sβ-Thalassemia and Their Association with Clinical and Hematological Features.</title>
            <link>http://www.medworm.com/index.php?rid=4067100&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20938172%26dopt%3DAbstract</link>
            <description>Conclusions: The prevalence of β(S)-haplotypes in this study is in agreement with the historical records of African slaves brought to the state of Minas Gerais. Furthermore, β(S)-haplotypes CAR and Ben were not associated with any analyzed feature of children with sickle cell anemia.
    PMID: 20938172 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4067100</comments>
            <pubDate>Mon, 11 Oct 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4067100</guid>        </item>
        <item>
            <title>High Prevalence of Helicobacter pylori Infection in Greek Patients with Myelodysplastic Syndromes.</title>
            <link>http://www.medworm.com/index.php?rid=4067104&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20938168%26dopt%3DAbstract</link>
            <description>Conclusion: Although there is no evidence for a causal relationship between Hp-I and MDS, the increased prevalence of Hp-I among the MDS patients is an interesting finding that deserves further investigation as it may indicate a common factor causing susceptibilities to both MDS and Hp-I or that Hp might influence the pathophysiology of MDS.
    PMID: 20938168 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4067104</comments>
            <pubDate>Sun, 10 Oct 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4067104</guid>        </item>
        <item>
            <title>Clofarabine-Based Regimen as Useful Bridge Therapy for Allogeneic Transplantation in Myeloid Blast Crisis of Philadelphia-Positive Chronic Myeloid Leukemia Resistant to Imatinib and Dasatinib.</title>
            <link>http://www.medworm.com/index.php?rid=4067103&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20938169%26dopt%3DAbstract</link>
            <description>Authors: Breccia M, Capria S, Iori AP, Foà R, Alimena G, Meloni G
    No abstract available.
    PMID: 20938169 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4067103</comments>
            <pubDate>Sun, 10 Oct 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4067103</guid>        </item>
        <item>
            <title>Sorafenib Treatment in 13 Patients with Acute Myeloid Leukemia and Activating FLT3 Mutations in Combination with Chemotherapy or as Monotherapy.</title>
            <link>http://www.medworm.com/index.php?rid=4067102&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20938170%26dopt%3DAbstract</link>
            <description>Authors: Schroeder T, Zohren F, Saure C, Bruns I, Czibere A, Safaian NN, Fenk R, Haas R, Kobbe G
    No abstract available.
    PMID: 20938170 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4067102</comments>
            <pubDate>Sun, 10 Oct 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4067102</guid>        </item>
        <item>
            <title>Prevention of Murine Acute Graft-versus-Host Disease by Recipient-Derived Paired Immunoglobulin-Like Receptor B Lentivirus-Transfected Dendritic Cells.</title>
            <link>http://www.medworm.com/index.php?rid=4031555&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20881379%26dopt%3DAbstract</link>
            <description>Authors: Zhao J, Luo Y, Wang X, Zhou H, Li Q, You Y, Zou P
    Direct interaction between T-suppressor and dendritic cells (DCs) results in DC tolerance by inducing upregulation of immunoglobulin-like transcript (ILT) 3 and ILT4. DCs were treated with a lentiviral vector containing paired immunoglobulin-like B gene (PIR-B) DCs and the effect of PIR-B-DCs on graft-versus-host disease (GVHD) was analyzed after allogeneic bone marrow (BM) transplantation (BMT). Therefore, 1 × 10(6) recipient-derived PIR-B-DCs were injected into BALB/c (H-2k(d)) mice using BM-splenocyte grafts from major histocompatibility complex-disparate C57BL/6 (H-2k(b)). Our results showed that PIR-B-DCs deficient in surface costimulatory molecules had higher PIR-B protein expression than immature DCs and interleukin 10-...</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4031555</comments>
            <pubDate>Tue, 28 Sep 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4031555</guid>        </item>
        <item>
            <title>Prohepcidin, B-Type Natriuretic Peptide, and Iron Status in a Cohort of Elderly Women from the Rhine-Ruhr Area.</title>
            <link>http://www.medworm.com/index.php?rid=4031556&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20881378%26dopt%3DAbstract</link>
            <description>Authors: Henry J, Casjens S, Schikowski T, Stachon A, Germing A, Ranft U, Lehnert M, Harth V, Krämer U, Brüning T, Pesch B
    No abstract available.
    PMID: 20881378 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4031556</comments>
            <pubDate>Mon, 27 Sep 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4031556</guid>        </item>
        <item>
            <title>A New Sickling Variant 'Hb S-Wake Î²[(Glu6Val-Asn139 Ser)]' Found in a Compound Heterozygote with Hb S Î²(Glu6Val) Coinherited with Homozygous Î±-Thalassemia-2: Phenotype and Molecular Characteristics.</title>
            <link>http://www.medworm.com/index.php?rid=4017918&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20861612%26dopt%3DAbstract</link>
            <description>We report the case of a 14-year-old African-American boy who was diagnosed with sickle cell disease. Laboratory tests showed that the patient was a compound heterozygote for a novel Hb variant with a double mutation detected on Î²(S) allele, Hb S Î²Glu6Val, and Î²Asn139Ser substitution, i.e. a Î²-chain variant named 'Hb S-Wake'. The patient also carried a single Hb S mutation in trans allele, leading to Hb SS-Wake disease. He had coinherited homozygous Î±(+)-thalassemia (-Î±(3.7)/-Î±(3.7)) simultaneously which resulted in multiple globin gene abnormalities.
    PMID: 20861612 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4017918</comments>
            <pubDate>Wed, 22 Sep 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4017918</guid>        </item>
        <item>
            <title>Association of Busulfan and Cyclophosphamide Conditioning with Sleep Disorders after Hematopoietic Stem Cell Transplantation.</title>
            <link>http://www.medworm.com/index.php?rid=4017917&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20861613%26dopt%3DAbstract</link>
            <description>Authors: Faulhaber GA, Furlanetto TW, Astigarraga CC, Moser Filho HL, Paludo AP, Silla LM
    New indications and conditioning regimens for hematopoietic stem cell transplantation (HSCT) have emerged in the last 10 years. Previous studies have shown the association of HSCT with late effects such as sleep disorders. The aim of this study was to determine the prevalence and factors associated with sleep disorders following HSCT in a population considering these new trends. Sixty-one individuals 1-10 years after allogeneic HSCT were surveyed using the DSM-IV-TR criteria for sleep disorders. Factors related to conditioning and graft-versus-host disease were collected from medical records. A prevalence of sleep disorders of 26.2% was found. Busulfan-cyclophosphamide conditioning was an independ...</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4017917</comments>
            <pubDate>Wed, 22 Sep 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4017917</guid>        </item>
        <item>
            <title>Secondary Erythrocytosis Caused by Hemoglobin Tak/(deltabeta)-Thalassemia Syndrome.</title>
            <link>http://www.medworm.com/index.php?rid=3958865&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20798489%26dopt%3DAbstract</link>
            <description>This report confirms the importance of both Hb and molecular investigations for the assessment of genotype/phenotype correlation and the appropriate management of the patients.
    PMID: 20798489 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3958865</comments>
            <pubDate>Wed, 25 Aug 2010 23:00:00 +0100</pubDate>
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        <item>
            <title>Detection of Elevated Serum Levels of the Chemokine CCL18 in B-Cell Chronic Lymphocytic Leukaemia: Identification of a Novel Biomarker.</title>
            <link>http://www.medworm.com/index.php?rid=3903999&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20733288%26dopt%3DAbstract</link>
            <description>Authors: SchrÃ¶ttner P, Wollner S, Catusse J, Burger M
    No abstract available.
    PMID: 20733288 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3903999</comments>
            <pubDate>Mon, 23 Aug 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3903999</guid>        </item>
        <item>
            <title>Response to Dasatinib in a Patient with Concomitant Chronic Myeloid Leukemia and Chronic Lymphocytic Leukemia.</title>
            <link>http://www.medworm.com/index.php?rid=3887223&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20720403%26dopt%3DAbstract</link>
            <description>Authors: Serpa M, Bendit I, Seguro F, Xavier F, Cavalcante M, Steinbaum D, Nardinelli L, Aldred VL, de Paula HM, Dorlhiac-Llacer PE
    While chronic lymphocytic leukemia (CLL) and chronic myeloid leukemia (CML) are common diseases in the elderly, they rarely occur simultaneously in the same patient. Here we present the case of a 77-year-old patient diagnosed with CML in the chronic phase who showed an optimal response to 400 mg/day of imatinib. This patient progressed to Binet B-CLL with an 11q22.3 deletion and CD38 positivity in the 4th month of treatment. During the follow-up, his lymphocyte number doubled in &amp;lt;6 months. Based on previous reports, dasatinib was chosen instead of imatinib. After 6 months of treatment with 100 mg/day of dasatinib, the patient demonstrated a partial resp...</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3887223</comments>
            <pubDate>Wed, 18 Aug 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3887223</guid>        </item>
        <item>
            <title>Lessons from a Case of Oromandibular Mucormycosis Treated with Surgery and a Combination of Amphotericin B Lipid Formulation plus Caspofungin.</title>
            <link>http://www.medworm.com/index.php?rid=3845580&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20689269%26dopt%3DAbstract</link>
            <description>Authors: Ojeda-Uribe M, Herbrecht R, Kiefer MH, Schultz P, Chain J, Chenard MP, Servant JM, Debry C
    A rare case of oromandibular Rhizopus oryzae infection is described in a 55-year-old woman with acute myeloid leukaemia and decompensated diabetes mellitus. The infection developed during induction chemotherapy when the patient was neutropenic. She was treated with a combination of amphotericin B lipid formulation and caspofungin plus surgery. Debridement surgery included excision of the lower lip, chin, floor of the mouth, a portion of the tongue, as well as mandibular resection at the level of the horizontal branches. Eight weeks of combined antifungal therapy were followed by secondary prophylaxis with amphotericin B lipid formulation during consolidation chemotherapy after achieving ...</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3845580</comments>
            <pubDate>Mon, 02 Aug 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3845580</guid>        </item>
        <item>
            <title>Unsuccessful Dasatinib Therapy in a Refractory Patient with Chronic Lymphocytic Leukemia.</title>
            <link>http://www.medworm.com/index.php?rid=3845579&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20689270%26dopt%3DAbstract</link>
            <description>Authors: Stagno F, Vigneri P, Del Fabro V, Fidilio A, Spina P, Massimino M, Messina A, Di Raimondo F
    
    PMID: 20689270 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3845579</comments>
            <pubDate>Mon, 02 Aug 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3845579</guid>        </item>
        <item>
            <title>Efficacy and Safety of Micafungin as an Empirical Antifungal Agent for Febrile Neutropenic Patients with Hematological Diseases.</title>
            <link>http://www.medworm.com/index.php?rid=3798949&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20664196%26dopt%3DAbstract</link>
            <description>Conclusion: Micafungin has an excellent efficacy (61.7%) and safety profile when used as an empirical antifungal agent in febrile neutropenic patients with hematological disorders.
    PMID: 20664196 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3798949</comments>
            <pubDate>Tue, 20 Jul 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3798949</guid>        </item>
        <item>
            <title>Bisphosphonates Induce Apoptosis of Circulating Endothelial Cells in Multiple Myeloma Patients and in Subjects with Bisphosphonate-Induced Osteonecrosis of the Jaws.</title>
            <link>http://www.medworm.com/index.php?rid=3768105&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20639624%26dopt%3DAbstract</link>
            <description>We examined the apoptosis of circulating endothelial progenitor cells in MM subjects before and after BP treatment and in osteonecrosis patients using a flow-cytometric analysis. Our data showed an increase in endothelial cell apoptosis in MM patients after BP administration and in osteonecrosis subjects. Our study seems in agreement with the hypothesis that BPs can inhibit angiogenesis interfering with endothelial cell proliferation and survival, leading to loss of blood vessels and avascular necrosis.
    PMID: 20639624 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3768105</comments>
            <pubDate>Wed, 14 Jul 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3768105</guid>        </item>
        <item>
            <title>Hemoglobin H Disease in Guangxi Province, Southern China: Clinical Review of 357 Patients.</title>
            <link>http://www.medworm.com/index.php?rid=3768104&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20639625%26dopt%3DAbstract</link>
            <description>Authors: Yin XL, Zhang XH, Zhou TH, Zhang TL, Luo RG, Wang L, Zhou YL, Chen YS, Kong XJ, Liang B, He YY, Peng L, Lu LB, Fang SP, Wu ZK
    The clinical characteristics of 357 patients with hemoglobin H (HbH) disease from the Guangxi province of Southern China were studied. One hundred and ninety-one (53.3%) patients were diagnosed with HbH-Constant Spring, 19 were diagnosed with HbH Westmead. Ten patients were shown to have coinherited HbH-Constant Spring/QS with a beta-thalassemia mutation. Coinheritance of the beta-thalassemia gene does not alleviate anemia (8.2 +/- 2.3 vs. 7.6 +/- 1.7 g/dl, p = 0.276), or influence age at diagnosis (20.2 +/- 19.6 vs. 12.9 +/- 11.0 years, p = 0.276). Ferritin levels were significantly higher in the group of patients with the nondeletional form of the dis...</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3768104</comments>
            <pubDate>Wed, 14 Jul 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3768104</guid>        </item>
        <item>
            <title>Apoptosis and Reduced Cell Proliferation of HL-60 Cell Line Caused by Human Telomerase Reverse Transcriptase Inhibition by siRNA.</title>
            <link>http://www.medworm.com/index.php?rid=3762576&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20628241%26dopt%3DAbstract</link>
            <description>Conclusion: The results indicated that hTERT siRNA resulted in 97.2 +/- 0.6% downregulation of the hTERT mRNA content; inhibition of the cell proliferation rate was about 52.8 +/- 2.3% and the apoptotic index of cells was 30.5 +/- 1.5%. hTERT plays an essential role in cell proliferation and control of the viability of leukemic cells, thus promising the development of drugs for leukemia.
    PMID: 20628241 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3762576</comments>
            <pubDate>Tue, 13 Jul 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3762576</guid>        </item>
        <item>
            <title>Autologous Hematopoietic Stem Cell Transplantation for Acute Myeloid Leukemia in First Complete Remission: A Meta-Analysis of Randomized Trials.</title>
            <link>http://www.medworm.com/index.php?rid=3743990&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20616541%26dopt%3DAbstract</link>
            <description>Conclusion: Our results support the conclusion that autologous SCT should not be considered as the first-line post-remission therapy for AML patients in CR1.
    PMID: 20616541 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3743990</comments>
            <pubDate>Fri, 09 Jul 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3743990</guid>        </item>
        <item>
            <title>Deferasirox Treatment Interruption in a Transfusion-Requiring Myelodysplastic Patient Led to Loss of Erythroid Response.</title>
            <link>http://www.medworm.com/index.php?rid=3743993&amp;cid=s_33499_19_f&amp;fid=33499&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20616538%26dopt%3DAbstract</link>
            <description>Authors: Breccia M, Loglisci G, Salaroli A, Cannella L, Santopietro M, Alimena G
    No abstract available.
    PMID: 20616538 [PubMed - as supplied by publisher] (Source: Acta Haematologica)</description>
            <author>Acta Haematologica</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3743993</comments>
            <pubDate>Thu, 08 Jul 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3743993</guid>        </item>
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