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        <title>Clinical and Laboratory Haematology 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 'Clinical and Laboratory Haematology' source.</description>
        <link><![CDATA[http://www.medworm.com/rss/search.php?qu=Clinical+and+Laboratory+Haematology&t=Clinical+and+Laboratory+Haematology&s=Search&f=source]]></link>
        <lastBuildDate>Wed, 08 Feb 2012 17:41:59 +0100</lastBuildDate>
        <item>
            <title>Correlation of the BRAF V600E mutation in hairy cell leukaemia with morphology, cytochemistry and immunophenotype</title>
            <link>http://www.medworm.com/index.php?rid=5668093&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2012.01402.x</link>
            <description>SummaryHairy cell leukaemia (HCL) has distinct clinical, morphological and immunophenotypic features with no recurrent cytogenetic or molecular abnormalities reported until the recent description of the BRAF V600E mutation in patients with classical HCL. The incidence of this mutation was sought in 27 patients with either classical HCL or HCL variant by an allele‐specific PCR approach and findings related to morphology, cytochemistry and immunophenotype. A high degree of correlation was noted between the presence of BRAF V600E and established diagnostic criteria in 26/27 patients with HCL/HCL variant. Detection of the BRAF V600E mutation is therefore a useful adjunct in the differential diagnosis of HCL and HCL variant and highlights the value of a multifaceted approach to the diagnosis ...</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5668093</comments>
            <pubDate>Wed, 01 Feb 2012 05:00:00 +0100</pubDate>
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        <item>
            <title>Analysis of polymorphisms of TNF‐α, LT‐α, IL‐10, IL‐12 and CTLA‐4 in patients with warm autoimmune haemolytic anaemia</title>
            <link>http://www.medworm.com/index.php?rid=5639114&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2012.01400.x</link>
            <description>Conclusion:  In this study, no significant differences on the frequency of TNF‐α, IL‐10, IL‐12 and CTLA‐4 polymorphisms between patients with AIHA and controls was found, suggesting that the targeted polymorphisms do not influence on the emergence and evolution of the disease. However, the LT‐α +252 polymorphism might have an effect for AIHAI development, suggesting that further studies are necessary to clear up this question. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5639114</comments>
            <pubDate>Sun, 29 Jan 2012 22:04:02 +0100</pubDate>
            <guid isPermaLink="false">5639114</guid>        </item>
        <item>
            <title>Role of gel test and flow cytometry in diagnosis of Coombs’ negative autoimmune haemolytic anaemia</title>
            <link>http://www.medworm.com/index.php?rid=5629852&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01397.x</link>
            <description>Conclusion:  Flow cytometry is more sensitive than GT for assessing CTT‐DAT‐negative AIHA. We propose that FC percent fluorescence cut‐off values should be employed to determine the Coombs’ negative AIHA cases. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5629852</comments>
            <pubDate>Thu, 26 Jan 2012 22:23:08 +0100</pubDate>
            <guid isPermaLink="false">5629852</guid>        </item>
        <item>
            <title>Molecular analysis of the β‐globin gene cluster haplotypes in a Sudanese population with sickle cell anaemia</title>
            <link>http://www.medworm.com/index.php?rid=5610032&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01388.x</link>
            <description>Conclusion:  βS Haplotyes were demonstrated successfully from dried blood samples. A new haplotype is apparent in Sudan, in addition to the four African haplotypes. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5610032</comments>
            <pubDate>Fri, 20 Jan 2012 21:58:25 +0100</pubDate>
            <guid isPermaLink="false">5610032</guid>        </item>
        <item>
            <title>Evaluation of cell population data on the UniCel DxH 800 Coulter Cellular Analysis system as a screening for viral infection in children</title>
            <link>http://www.medworm.com/index.php?rid=5583357&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01392.x</link>
            <description>Conclusion:  In conclusion, the implementation of leukocytes CPD parameters can be useful in the detection of viral infection in children. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5583357</comments>
            <pubDate>Sat, 14 Jan 2012 07:27:23 +0100</pubDate>
            <guid isPermaLink="false">5583357</guid>        </item>
        <item>
            <title>Mean platelet volume: comparison of three analysers towards standardization of platelet morphological phenotype</title>
            <link>http://www.medworm.com/index.php?rid=5583358&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01396.x</link>
            <description>Conclusion:  To harmonize our procedures, we propose definitions of platelet size (normal size, macroplatelets and giant platelets) based on the coordinated interpretation of the MPV, the distribution of platelet volume and the morphological appearance. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5583358</comments>
            <pubDate>Mon, 09 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5583358</guid>        </item>
        <item>
            <title>Falciparum malaria parasitemia index for predicting severe malaria</title>
            <link>http://www.medworm.com/index.php?rid=5561185&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01398.x</link>
            <description>Conclusion:  Symptoms of severe falciparum malaria depend on many factors. For the definition of hyperparasitemia in areas of low or seasonal transmission, peripheral parasitemia of 0.5% might be considered a cutoff point for discrimination between severity levels. This value might be useful for the clinical management of malaria, particularly in hypo‐endemic areas, unstable transmission areas, and other areas with similar transmission patterns. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5561185</comments>
            <pubDate>Thu, 05 Jan 2012 21:46:06 +0100</pubDate>
            <guid isPermaLink="false">5561185</guid>        </item>
        <item>
            <title>Mixed phenotype acute leukemia of T/myeloid type with a prominent cellular heterogeneity and unique karyotypic aberration 45,XY, dic(11;17)</title>
            <link>http://www.medworm.com/index.php?rid=5553038&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01393.x</link>
            <description>Conclusion.  A case of MPAL with complex biological features, 45,XY, dic(11;17)(11qter→11p11.2::17p11.2→17qter) karyotype and an aggressive, therapy‐resistant clinical course, is presented. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5553038</comments>
            <pubDate>Sat, 31 Dec 2011 20:02:41 +0100</pubDate>
            <guid isPermaLink="false">5553038</guid>        </item>
        <item>
            <title>Neutrophil cell population data: useful indicators for postsurgical bacterial infection</title>
            <link>http://www.medworm.com/index.php?rid=5553039&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01394.x</link>
            <description>Conclusion:  Neutrophil CPD, MNV, and NDW are better indicators for postoperative bacterial infection. The potential clinical usefulness of these parameters merits further exploration in a larger prospective study. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5553039</comments>
            <pubDate>Thu, 29 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5553039</guid>        </item>
        <item>
            <title>Molecular and genetic features of myelodysplastic syndromes</title>
            <link>http://www.medworm.com/index.php?rid=5545181&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01390.x</link>
            <description>SummaryMultifactorial pathogenetic features underlying myelodysplastic syndromes (MDS) relate to inherent abnormalities within the hematopoietic precursor cell population. The predominant final common pathogenetic pathway causing ineffective hematopoiesis in MDS has been the varying degrees of apoptosis of the hematopoietic precursors and their progeny. A variety of molecular abnormalities have been demonstrated in MDS. These lesions are attributable to nonrandom cytogenetic and oncogenic mutations, indicative of chromosomal and genetic instability, transcriptional RNA splicing abnormalities, and epigenetic changes. Evolutionary cytogenetic changes may occur during the course of the disorder, which are associated with disease progression. These genetic derangements reflect a multistep proc...</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5545181</comments>
            <pubDate>Wed, 28 Dec 2011 13:53:50 +0100</pubDate>
            <guid isPermaLink="false">5545181</guid>        </item>
        <item>
            <title>List of Reviewers</title>
            <link>http://www.medworm.com/index.php?rid=5526235&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01395.x</link>
            <description>(Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5526235</comments>
            <pubDate>Thu, 22 Dec 2011 10:27:21 +0100</pubDate>
            <guid isPermaLink="false">5526235</guid>        </item>
        <item>
            <title>Proteasome inhibitor bortezomib overcomes P‐gp‐mediated multidrug resistance in resistant leukemic cell lines</title>
            <link>http://www.medworm.com/index.php?rid=5477388&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01384.x</link>
            <description>Conclusion:  Bortezomib is a promising potential therapy for acute leukemia, especially mdr1 drug‐resistant leukemia. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5477388</comments>
            <pubDate>Wed, 07 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5477388</guid>        </item>
        <item>
            <title>Microscopic examination of bone marrow aspirate in healthy adults – comparison of two techniques of slide preparation</title>
            <link>http://www.medworm.com/index.php?rid=5477387&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01387.x</link>
            <description>Conclusions:  The crush technique seems to be more valuable than the wedge‐spread technique because of the lack of a blood dilution effect and better assessment of megakaryopoiesis. We recommend the crush technique for the evaluation of the percentage composition of bone marrow cells. In a very small number of patients with irregular cell localization in the bone marrow particles, the wedge‐spread technique may be more beneficial for the assessment of total cellularity. The recommendation to routinely prepare slides using both of these techniques is fully justified. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5477387</comments>
            <pubDate>Wed, 07 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5477387</guid>        </item>
        <item>
            <title>Association of Janus kinase 2 (JAK2) polymorphisms with acute leukemia susceptibility</title>
            <link>http://www.medworm.com/index.php?rid=5506082&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01386.x</link>
            <description>Conclusion:  The results indicate that the risk of acute leukemia might be associated with JAK2 polymorphisms. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5506082</comments>
            <pubDate>Thu, 01 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5506082</guid>        </item>
        <item>
            <title>New erythrocyte and reticulocyte parameters on CELL‐DYN Sapphire: analytical and preanalytical aspects</title>
            <link>http://www.medworm.com/index.php?rid=5487856&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01391.x</link>
            <description>Conclusions:  The new RBC parameters of CELL‐DYN Sapphire generally correlated well with those of Advia 120, although significant systematic differences were present, particularly in reticulocyte MCH and MCV. These differences necessitate instrument‐specific reference ranges and clinical decision values. To minimize preanalytical effects, these parameters should be measured in fresh blood samples. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5487856</comments>
            <pubDate>Thu, 01 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5487856</guid>        </item>
        <item>
            <title>Analysis of altered proteins related to blast crisis in chronic myeloid leukemia by proteomic study</title>
            <link>http://www.medworm.com/index.php?rid=5477386&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01389.x</link>
            <description>Conclusion:  A group of proteins associated with BC can be obtained and the result of this study might provide clues for further research. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5477386</comments>
            <pubDate>Thu, 01 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5477386</guid>        </item>
        <item>
            <title>A rare case of Lennert’s type peripheral T‐cell lymphoma with t(14;19)(q11.2;q13.3)</title>
            <link>http://www.medworm.com/index.php?rid=5458838&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01385.x</link>
            <description>We describe here a rare chromosomal rearrangement, t(14;19)(q11.2;q13.3), in a Lennert’s lymphoma, a variant of PTCL, not otherwise specified. Sequential fluorescence in situ hybridization assays showed that the breakpoint in 19q13.3 was located distal to the BCL3 and PVRL2 genes, both of which may be candidate proto‐oncogenes. These findings suggest that another gene is involved in the pathogenic characteristics observed in this patient with Lennert’s lymphoma. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5458838</comments>
            <pubDate>Thu, 01 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5458838</guid>        </item>
        <item>
            <title>The relationship of leukocyte anisocytosis to holotranscobalamin, a marker of cobalamin deficiency</title>
            <link>http://www.medworm.com/index.php?rid=5409579&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01382.x</link>
            <description>Conclusion:  In this collective of subjectively healthy elderly individuals, monocyte anisocytosis, neutrophil anisocytosis and mean lymphocyte volume were associated with decreased HoloTC. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5409579</comments>
            <pubDate>Thu, 17 Nov 2011 01:23:48 +0100</pubDate>
            <guid isPermaLink="false">5409579</guid>        </item>
        <item>
            <title>ICSH recommendations for identification, diagnostic value, and quantitation of schistocytes</title>
            <link>http://www.medworm.com/index.php?rid=5409580&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01380.x</link>
            <description>SummarySchistocytes are fragments of red blood cells (RBCs) produced by extrinsic mechanical damage within the circulation. The detection of schistocytes is an important morphological clue to the diagnosis of thrombotic microangiopathic anemia (TMA). Reporting criteria between different laboratories, however, are not uniform, owing to variability of shape and nature of fragments, as well as subjectivity and heterogeneity in their morphological assessment. Lack of standardization may lead to inconsistency or misdiagnosis, thereby affecting treatment and clinical outcome. The Schistocyte Working Group of the International Council for Standardization in Haematology (ICSH) has prepared specific recommendations to standardize schistocyte identification, enumeration, and reporting. They deal wit...</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5409580</comments>
            <pubDate>Tue, 15 Nov 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5409580</guid>        </item>
        <item>
            <title>A new simple approach for the determination of pyrimidine 5′‐nucleotidase activity in human erythrocytes using an ELISA reader</title>
            <link>http://www.medworm.com/index.php?rid=5409581&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01381.x</link>
            <description>Conclusion:  Determination of P5′N‐1 activity by using an ELISA reader is a new, simple, less time consuming and reliable method. It also avoids the use of radioactive material or HPLC which is a significant advantage. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5409581</comments>
            <pubDate>Mon, 14 Nov 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5409581</guid>        </item>
        <item>
            <title>Sensitive detection and accurate monitoring of Plasmodium vivax parasites on routine complete blood count using automatic blood cell analyzer (DxH800TM)</title>
            <link>http://www.medworm.com/index.php?rid=5401341&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01383.x</link>
            <description>Conclusion:  DxH800™ provides very sensitive and specific, easily recognizable P. vivax malaria signals on routine CBC without need for the additional reagents or special procedures. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5401341</comments>
            <pubDate>Sun, 13 Nov 2011 10:11:46 +0100</pubDate>
            <guid isPermaLink="false">5401341</guid>        </item>
        <item>
            <title>Scanning electron microscopy analysis of erythrocytes in thromboembolic ischemic stroke</title>
            <link>http://www.medworm.com/index.php?rid=5388795&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01379.x</link>
            <description>Conclusion:  We suggest that in healthy individuals, a typical smear would contain several nondiscoid‐shaped erythrocytes, only clearly visible at high magnification. However, thromboembolic ischemic stroke does significantly impact erythorcyte shape, and this change in morphology may result in an impaired microcirculation, as well as impaired oxygen carrying capacity. This changed morphology may further complicate the restoring of homeostasis caused by acute thromboembolic stroke. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5388795</comments>
            <pubDate>Thu, 10 Nov 2011 11:29:59 +0100</pubDate>
            <guid isPermaLink="false">5388795</guid>        </item>
        <item>
            <title>Influence of in vitro hemolysis on hematological testing on Advia 2120</title>
            <link>http://www.medworm.com/index.php?rid=5388796&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01378.x</link>
            <description>Conclusion:  The results of routine hematological testing on mildly to frankly hemolyzed specimens might be unreliable. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5388796</comments>
            <pubDate>Wed, 02 Nov 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5388796</guid>        </item>
        <item>
            <title>New guidelines for lupus anticoagulant: sensitivity and specificity of cut‐off values calculated with plasmas from healthy controls in mixing and confirmatory tests</title>
            <link>http://www.medworm.com/index.php?rid=5362624&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01376.x</link>
            <description>Conclusion:  The combination of mixing and confirmatory tests interpreted according to the new guidelines can clearly differentiate LA from other coagulopathies. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5362624</comments>
            <pubDate>Wed, 02 Nov 2011 00:24:11 +0100</pubDate>
            <guid isPermaLink="false">5362624</guid>        </item>
        <item>
            <title>Decreased blood catalase activity is not related to specific beta‐thalassemia mutations in Hungary</title>
            <link>http://www.medworm.com/index.php?rid=5316311&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01377.x</link>
            <description>Conclusion:  The decrease in blood catalase activity might be due to the damaging effects of free radicals on the catalase protein. Consequently, these beta‐thalassemia trait patients may be relatively susceptible to damage caused by oxidative stress. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5316311</comments>
            <pubDate>Sat, 01 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5316311</guid>        </item>
        <item>
            <title>ICSH recommendations for the measurement of Haemoglobin A2</title>
            <link>http://www.medworm.com/index.php?rid=5286650&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01368.x</link>
            <description>SummaryAlthough DNA analysis is needed for characterization of the mutations that cause β‐thalassaemia, measurement of the Hb A2 is essential for the routine identification of people who are carriers of β‐thalassaemia. The methods of quantitating Hb A2 are described together with pitfalls in undertaking these laboratory tests with particular emphasis on automated high‐performance liquid chromatography and capillary electrophoresis. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5286650</comments>
            <pubDate>Sat, 01 Oct 2011 04:00:00 +0100</pubDate>
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        <item>
            <title>Type 2 polarized immune response holds a major position in Epstein–Barr virus‐related idiopathic thrombocytopenic purpura (EBV‐ITP)</title>
            <link>http://www.medworm.com/index.php?rid=5261782&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01375.x</link>
            <description>Conclusion:  Our findings clearly show that type 2 polarization of the autoimmune response accounts for the expression of cytokines and transcription factors in EBV‐ITP. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5261782</comments>
            <pubDate>Thu, 29 Sep 2011 09:50:58 +0100</pubDate>
            <guid isPermaLink="false">5261782</guid>        </item>
        <item>
            <title>ICSH recommendations for the measurement of Haemoglobin F</title>
            <link>http://www.medworm.com/index.php?rid=5227152&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01367.x</link>
            <description>SummaryMeasurement of the Haemoglobin F in red cell haemolysates is important in the diagnosis of δβ thalassaemia, hereditary persistence of fetal haemoglobin (HPFH) and in the diagnosis and management of sickle cell disease. The distribution of Hb F in red cells is useful in the diagnosis of HPFH and in the assessment of feto‐maternal haemorrhage. The methods of quantifying Hb F are described together with pitfalls in undertaking these laboratory tests with particular emphasis on automated high‐performance liquid chromatography and capillary electrophoresis. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5227152</comments>
            <pubDate>Mon, 19 Sep 2011 02:33:35 +0100</pubDate>
            <guid isPermaLink="false">5227152</guid>        </item>
        <item>
            <title>State of the art in natural killer cell malignancies</title>
            <link>http://www.medworm.com/index.php?rid=5197009&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01374.x</link>
            <description>SummaryThe recently updated World Health Organization (WHO) classification of tumors of hematopoietic and lymphoid tissues, published in 2008, has made great advances in revising the disorders previously included in the pool of natural killer (NK) cell tumors. Although NK cell neoplasms represent a relatively rare group of diseases, accounting for &amp;lt;5% of all lymphoid neoplasms, they include very distinctive conditions both clinically and pathologically. This family of diseases includes the most indolent clinical forms, such as the provisional new entry of chronic lymphoproliferative disorder of NK cells (CLPD‐NK) in the WHO classification, as well as one of the most fatal diseases recognized in medical oncology, aggressive NK cell leukemia (ANKL), which is characterized by a prognosis...</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5197009</comments>
            <pubDate>Wed, 07 Sep 2011 07:48:13 +0100</pubDate>
            <guid isPermaLink="false">5197009</guid>        </item>
        <item>
            <title>Hemoglobin Lepore Hollandia in India</title>
            <link>http://www.medworm.com/index.php?rid=5197011&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01372.x</link>
            <description>Conclusion:  Hemoglobin Lepore Hollandia is a relatively uncommon variant in the Indian population and can be identified using a combination of chromatographic, electrophoretic, and molecular analysis. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5197011</comments>
            <pubDate>Mon, 05 Sep 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5197011</guid>        </item>
        <item>
            <title>Counting of leukocytes in samples from G‐CSF mobilized donors, leukapheresis products, and cord blood: the performances of an analyzer with dedicated profiles</title>
            <link>http://www.medworm.com/index.php?rid=5197010&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01373.x</link>
            <description>Conclusion:  The ABX Pentra DX 120 provided accurate WBC count and differential count during MB, LP, and CB analyses and allowed a better characterization of donors’ hematologic status and graft composition. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5197010</comments>
            <pubDate>Mon, 05 Sep 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5197010</guid>        </item>
        <item>
            <title>Corrigendum</title>
            <link>http://www.medworm.com/index.php?rid=5163387&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01366.x</link>
            <description>(Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5163387</comments>
            <pubDate>Sat, 27 Aug 2011 16:24:31 +0100</pubDate>
            <guid isPermaLink="false">5163387</guid>        </item>
        <item>
            <title>The role of molecular genetic analysis within the diagnostic haemato‐oncology laboratory</title>
            <link>http://www.medworm.com/index.php?rid=5163381&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01364.x</link>
            <description>SummaryThe identification of the molecular genetic basis to many haematological malignancies along with the increased use of molecularly targeted therapy has heralded an increasing role for molecular genetic–based techniques. Demonstration of acquired changes such as the JAK2 V617F mutation within myeloproliferative neoplasms has quickly moved from a research setting to the diagnostic laboratory. Disease‐specific genetic markers, such as the BCR–ABL1 fusion gene in chronic myeloid leukaemia, enable sensitive molecular genetic methods to be applied for the detection and quantification of low‐level residual disease, allowing early identification of relapse. Consequently, molecular genetics now plays a crucial role in diagnosis, the identification of prognostic markers and monitoring ...</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5163381</comments>
            <pubDate>Sat, 27 Aug 2011 16:23:53 +0100</pubDate>
            <guid isPermaLink="false">5163381</guid>        </item>
        <item>
            <title>Quantification of hemoglobin Constant Spring in heterozygote and homozygote by a capillary electrophoresis method</title>
            <link>http://www.medworm.com/index.php?rid=5163382&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01371.x</link>
            <description>Conclusion:  CE is the preferable method for screening of heterozygote and homozygote of Hb CS. Moreover, in conjunction with a lower MCV (&amp;lt;70 fL), this approach provided a high resolution to identify Hb H‐CS disease. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5163382</comments>
            <pubDate>Thu, 25 Aug 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5163382</guid>        </item>
        <item>
            <title>State of the art in myeloid sarcoma</title>
            <link>http://www.medworm.com/index.php?rid=5163385&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01361.x</link>
            <description>Conclusion:  A minimal panel of immunohistochemical markers should include anti‐CD43 or anti‐lysozyme as a lack of immunoreactivity for either of these sensitive markers would be inconsistent with a diagnosis of myeloid sarcoma. Use of more specific markers of myeloid disease, such as CD33, myeloperoxidase, CD34 and CD117 is necessary to establish the diagnosis. Other antibodies may be added depending on the differential diagnosis. Identification of acute myeloid leukemia‐associated genetic lesions may be helpful in arriving at the correct diagnosis. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5163385</comments>
            <pubDate>Tue, 23 Aug 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5163385</guid>        </item>
        <item>
            <title>The use of the white cell count and haemoglobin in combination as an effective screen to predict the normality of the full blood count</title>
            <link>http://www.medworm.com/index.php?rid=5163384&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01365.x</link>
            <description>Conclusion:  We concluded that in the presence of a normal WBC and haemoglobin, the FBC is normal in almost all cases and measuring these two parameters could be used as an effective screen to predict FBC normality. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5163384</comments>
            <pubDate>Tue, 23 Aug 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5163384</guid>        </item>
        <item>
            <title>Plasma protein oxidation is correlated positively with plasma iron levels and negatively with hemolysate zinc levels in sickle‐cell anemia patients</title>
            <link>http://www.medworm.com/index.php?rid=5163383&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01369.x</link>
            <description>Conclusion:  Alterations of proteins, lipids, and ions in the plasma and erythrocyte of steady‐state patients with SCA were demonstrated. Some of these alterations are related with each other and with the oxidative stress observed in the disease. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5163383</comments>
            <pubDate>Tue, 23 Aug 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5163383</guid>        </item>
        <item>
            <title>A novel test tube method of screening for hemoglobin E</title>
            <link>http://www.medworm.com/index.php?rid=5163386&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01357.x</link>
            <description>Conclusion:  The described novel test tube method could be an alternative method of mass population screening for HbE, particularly in small health care facilities. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5163386</comments>
            <pubDate>Mon, 22 Aug 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5163386</guid>        </item>
        <item>
            <title>Differentiating between intra‐ and extracellular chemiluminescence in diluted whole‐blood samples</title>
            <link>http://www.medworm.com/index.php?rid=5120452&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01370.x</link>
            <description>Conclusion:  Measurement of Ca‐I‐activated CL enhanced with 10−4 m luminol is recommended for the detection of intracellular ROS. The addition of HRP leads to the detection of overall ROS production while the OZP‐activated system with its addition of HRP can only be used to detect overall ROS production. Ca‐I‐activated CL enhanced with 10−4 m isoluminol and with addition of HRP is recommended for the detection of extracellular CL. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5120452</comments>
            <pubDate>Sun, 31 Jul 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5120452</guid>        </item>
        <item>
            <title>Accuracy and precision of hemoglobin point‐of‐care testing during major pediatric surgery</title>
            <link>http://www.medworm.com/index.php?rid=5070551&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01363.x</link>
            <description>Conclusion:  All POCT devices tested and operated by trained staff for hemoglobinometry showed reliable test results. They all allow for simple, fast, and precise bedside determination of hemoglobin concentration in the intraoperative setting. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5070551</comments>
            <pubDate>Thu, 28 Jul 2011 04:59:55 +0100</pubDate>
            <guid isPermaLink="false">5070551</guid>        </item>
        <item>
            <title>Centrifugation speed affects light transmission aggregometry</title>
            <link>http://www.medworm.com/index.php?rid=5070553&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01360.x</link>
            <description>Conclusion:  Our data demonstrate the importance of centrifugation speed in the interpretation of LTA results, supporting the need for standardization of centrifugation RCF in LTA protocols. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5070553</comments>
            <pubDate>Tue, 26 Jul 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5070553</guid>        </item>
        <item>
            <title>Distinguishing types 1 and 2M von Willebrand disease</title>
            <link>http://www.medworm.com/index.php?rid=5070552&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01362.x</link>
            <description>We describe a case of 2M VWD ‘masquerading’ as type 1 and show how the differential diagnosis can be obtained using standard laboratory assays. The case was genetically confirmed as a 3943C&amp;gt;T mutation, leading to R1315C. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5070552</comments>
            <pubDate>Tue, 26 Jul 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5070552</guid>        </item>
        <item>
            <title>The relevance of HPA‐15 antigen expression for anti‐HPA‐15 antibody detection</title>
            <link>http://www.medworm.com/index.php?rid=5031258&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01358.x</link>
            <description>Conclusion:  Anti‐HPA‐15 antibody detection should be based on carefully selected platelets with high HPA‐15 expression level. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5031258</comments>
            <pubDate>Sat, 16 Jul 2011 17:30:08 +0100</pubDate>
            <guid isPermaLink="false">5031258</guid>        </item>
        <item>
            <title>Management of patients receiving oral anticoagulants using computer dosing software – does everyone agree? Data from a UK NEQAS (blood coagulation) exercise</title>
            <link>http://www.medworm.com/index.php?rid=5031259&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01359.x</link>
            <description>Conclusion:  The study emphasizes large variation in the approach to managing these scenarios and warrants further investigation, together with education including promoting national guidelines for the assignment of target ranges. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5031259</comments>
            <pubDate>Wed, 13 Jul 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5031259</guid>        </item>
        <item>
            <title>Myeloperoxidase staining with diluted Giemsa with phosphate buffer of pH 6.8 as a counterstain</title>
            <link>http://www.medworm.com/index.php?rid=5000037&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01352.x</link>
            <description>(Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5000037</comments>
            <pubDate>Wed, 06 Jul 2011 15:51:15 +0100</pubDate>
            <guid isPermaLink="false">5000037</guid>        </item>
        <item>
            <title>Low hemoglobin density potential marker of iron availability</title>
            <link>http://www.medworm.com/index.php?rid=5000039&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01355.x</link>
            <description>Conclusion:  LHD% is a reliable parameter for the detection of iron deficiency in patients with anemia in the presence of inflammation. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5000039</comments>
            <pubDate>Sun, 03 Jul 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5000039</guid>        </item>
        <item>
            <title>Platelet activation, coagulation activation and C‐reactive protein in simultaneous samples from the vascular access and peripheral veins of haemodialysis patients</title>
            <link>http://www.medworm.com/index.php?rid=5000038&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01356.x</link>
            <description>Conclusion:  There are statistically significant differences between sampling sites, although samples from the VA do not appear to be more pro‐thrombotic. Future studies comparing HD patients with controls should ensure uniformity of sampling sites to prevent inaccurate conclusions being drawn. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5000038</comments>
            <pubDate>Sun, 03 Jul 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5000038</guid>        </item>
        <item>
            <title>Production and characterization of liquid‐stored and lyophilized reconstituted human infusible platelet membranes</title>
            <link>http://www.medworm.com/index.php?rid=4978205&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01354.x</link>
            <description>Conclusion:  This study revealed the potential of IPM microvesicles to mimic the binding features of platelets in vitro. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4978205</comments>
            <pubDate>Wed, 29 Jun 2011 18:03:13 +0100</pubDate>
            <guid isPermaLink="false">4978205</guid>        </item>
        <item>
            <title>Clinical course and molecular features in 21 patients with atypical chronic myeloid leukemia</title>
            <link>http://www.medworm.com/index.php?rid=5197012&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01351.x</link>
            <description>(Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5197012</comments>
            <pubDate>Sun, 26 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5197012</guid>        </item>
        <item>
            <title>Investigation of inflicted injury in a young girl reveals mild haemophilia A and Turner’s syndrome</title>
            <link>http://www.medworm.com/index.php?rid=4978209&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01347.x</link>
            <description>SummaryA 2‐year‐old girl presented to casualty with a right knee effusion after apparently minor trauma. Inflicted injury was suspected and full forensic coagulation studies were performed which revealed a mild deficiency of factor VIII. Screening of the exons and intron/exon boundaries of F8 gene indicated that the child appeared to be homozygous for the missense mutation c.5123G&amp;gt;A (p.Arg1708His) in exon 14 of the F8 gene. This mutation has been reported to be associated with mild haemophilia A. The possibility of hemizygosity had been masked by the test kit employed but referral to the genetics service and subsequent array CGH resulted in a diagnosis of Turner syndrome. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4978209</comments>
            <pubDate>Sun, 26 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4978209</guid>        </item>
        <item>
            <title>Reticulocyte and haemoglobin profiles in elite triathletes over four consecutive seasons</title>
            <link>http://www.medworm.com/index.php?rid=4978208&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01348.x</link>
            <description>Conclusion:  We conclude that Ret % and [Hb] remain stable over four consecutive seasons in elite triathletes, confirming that both parameters are valid for antidoping purposes based on the Blood Passport. In addition, Ret % fluctuations within one season require further investigation in females. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4978208</comments>
            <pubDate>Sun, 26 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4978208</guid>        </item>
        <item>
            <title>On‐demand but not prophylactic treatment with FVIII concentrate increase thrombin activatable fibrinolysis inhibitor activation in severe haemophilia A patients</title>
            <link>http://www.medworm.com/index.php?rid=4978207&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01349.x</link>
            <description>Conclusion:  These findings suggest that in patients to whom FVIII is administered on demand the fibrinolysis activity is more down regulated than in patients following a prophylactic treatment regime. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4978207</comments>
            <pubDate>Sun, 26 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4978207</guid>        </item>
        <item>
            <title>Letter to the Editor</title>
            <link>http://www.medworm.com/index.php?rid=4978206&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01351.x</link>
            <description>(Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4978206</comments>
            <pubDate>Sun, 26 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4978206</guid>        </item>
        <item>
            <title>Using the laboratory to predict recurrent venous thrombosis</title>
            <link>http://www.medworm.com/index.php?rid=4962056&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01345.x</link>
            <description>SummaryCharacterisation of heritable thrombophilic defects has facilitated an understanding of the complex mechanisms influencing risk of venous thromboembolism. In parallel with this, the importance of gene–environment interaction in the development of this disease has become apparent. However, testing for a limited number of heritable thrombophilic defects (first generation thrombophilia testing) has not been shown to predict likelihood of recurrent venous thrombosis to any useful degree. This paradox whereby thrombophilia testing identifies defects associated with an increased risk of a first venous thrombosis but not of a particularly high risk of recurrence is likely the result of limitations imposed by a limited dichotomous testing strategy compounded by test inaccuracy and impreci...</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4962056</comments>
            <pubDate>Fri, 24 Jun 2011 14:51:43 +0100</pubDate>
            <guid isPermaLink="false">4962056</guid>        </item>
        <item>
            <title>Repeat haematinic requests in patients with previous normal results: the scale of the problem in elderly patients at a district general hospital</title>
            <link>http://www.medworm.com/index.php?rid=4962054&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01350.x</link>
            <description>This study aimed to quantify unnecessary repeat haematinic tests taken from the elderly in a district general hospital. Haematinic tests (ferritin, B12, serum folate) from patients age ≥70 years were reviewed for repeat tests during an 8‐week period. Questionnaires were given to doctors to establish when the considered repeating a ‘borderline low normal’ result to be clinically justifiable. 7.7% of all haematinic tests were repeat tests and of these, the majority (83%) was performed following a previously normal result. Thirteen of 24 doctors believed repeating a normal result at the bottom of the normal range (‘borderline low normal’) was justifiable. After excluding ‘borderline low normal’ results, 6.0% (at minimum) of repeat tests were done following a previous normal ...</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4962054</comments>
            <pubDate>Fri, 24 Jun 2011 14:50:58 +0100</pubDate>
            <guid isPermaLink="false">4962054</guid>        </item>
        <item>
            <title>A novel, variant BCR‐ABL1 transcript not detected by standard real‐time quantitative PCR in a patient with chronic myeloid leukaemia</title>
            <link>http://www.medworm.com/index.php?rid=4962055&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01346.x</link>
            <description>(Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4962055</comments>
            <pubDate>Tue, 21 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4962055</guid>        </item>
        <item>
            <title>Left Shift 1+ flag for the detection of band neutrophils: interlaboratory variations and recommendations for the routine laboratory</title>
            <link>http://www.medworm.com/index.php?rid=4938768&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01340.x</link>
            <description>Conclusion: ; Critical control of the factors influencing the LS1+ flag can significantly decrease the number of microscopic samples to be reviewed and may be valuable for every laboratory performing routine differentials, using any type of hematology analyzer. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4938768</comments>
            <pubDate>Wed, 15 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4938768</guid>        </item>
        <item>
            <title>MRD analysis and treatment outcome in three children with SET‐NUP214‐positive hematological malignancies</title>
            <link>http://www.medworm.com/index.php?rid=4938767&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01343.x</link>
            <description>(Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4938767</comments>
            <pubDate>Wed, 15 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4938767</guid>        </item>
        <item>
            <title>Assessment of antithrombin deficiency in the real world</title>
            <link>http://www.medworm.com/index.php?rid=4938766&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01341.x</link>
            <description>(Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4938766</comments>
            <pubDate>Wed, 15 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4938766</guid>        </item>
        <item>
            <title>Genotyping of human platelet antigen‐15 by single closed‐tube Tm‐shift method</title>
            <link>http://www.medworm.com/index.php?rid=4923885&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01344.x</link>
            <description>Conclusion:  The single closed‐tube Tm‐shift method for HPA‐15 genotyping is high‐throughput, rapid, reliable, reproducible and cost‐effective and it is superior to conventional PCR‐SSP used in routine genotyping of HPA‐15. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4923885</comments>
            <pubDate>Sun, 12 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4923885</guid>        </item>
        <item>
            <title>Assessment for antithrombin deficiency in the real world</title>
            <link>http://www.medworm.com/index.php?rid=4923884&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01342.x</link>
            <description>(Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4923884</comments>
            <pubDate>Sun, 12 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4923884</guid>        </item>
        <item>
            <title>D‐dimer level in pediatric patients with solid and hematologic malignancies, Shiraz, Southern Iran</title>
            <link>http://www.medworm.com/index.php?rid=4904889&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01337.x</link>
            <description>(Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4904889</comments>
            <pubDate>Sun, 05 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4904889</guid>        </item>
        <item>
            <title>Complete blood count using VCS (volume, conductivity, light scatter) technology is affected by hyperlipidemia in a child with acute leukemia</title>
            <link>http://www.medworm.com/index.php?rid=4904888&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01333.x</link>
            <description>We describe a case of l‐asparaginase‐associated severe hyperlipidemia with complete blood count abnormalities. Complete blood count analysis was performed with Beckman COULTER® GEN·S™ system, which uses the Coulter Volume, Conductivity, Scatter technology to probe hydrodynamically focused cells. Although an expected significant inaccuracy in hemoglobin determination occurred starting from a lipid value of 3450 mg/dl, we observed that triglyceride level was 1466 mg/dl. Complete blood count analysis revealed that exceptionally high hemoglobin, mean corpuscular hemoglobin, and mean corpuscular hemoglobin concentration levels vs. discordant with red blood cell count, mean corpuscular volume, and hematocrit levels. Total leukocyte count altered spontaneously in a wide range, and was...</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4904888</comments>
            <pubDate>Sun, 05 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4904888</guid>        </item>
        <item>
            <title>Accurate testing for dysfunctional molecules: the potential for missing the diagnosis</title>
            <link>http://www.medworm.com/index.php?rid=4938765&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01353.x</link>
            <description>(Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4938765</comments>
            <pubDate>Tue, 31 May 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4938765</guid>        </item>
        <item>
            <title>Automated vs. manual cerebrospinal fluid cell counts: a work and cost analysis comparing the Sysmex XE‐5000 and the Fuchs–Rosenthal manual counting chamber</title>
            <link>http://www.medworm.com/index.php?rid=4923883&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01339.x</link>
            <description>Conclusion:  Our study revealed a lower mean CV for the total cell count for the XE‐5000 method. The fully automated CSF cell count results in a 7.5‐fold reduction in TAT and leads to a significant decrease in total analytical performance costs. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4923883</comments>
            <pubDate>Tue, 31 May 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4923883</guid>        </item>
        <item>
            <title>Serum levels of granulocyte colony‐stimulating factor in JAK2 V617F ‐positive vs. negative erythrocytosis</title>
            <link>http://www.medworm.com/index.php?rid=4904887&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01336.x</link>
            <description>(Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4904887</comments>
            <pubDate>Tue, 31 May 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4904887</guid>        </item>
        <item>
            <title>Evaluation of the nucleated red blood cell count in neonates using the Beckman Coulter UniCel DxH 800 analyzer</title>
            <link>http://www.medworm.com/index.php?rid=4886286&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01335.x</link>
            <description>Conclusion:  The results obtained indicate the UniCel DxH 800 to be an excellent test on neonatal blood and superior to the other analyzers. Therefore, the DxH 800 is an effective and highly sensitive system for the analysis of NRBCs on newborns. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4886286</comments>
            <pubDate>Tue, 31 May 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4886286</guid>        </item>
        <item>
            <title>Precise quantification of haemoglobin in erythroid precursors and plasma</title>
            <link>http://www.medworm.com/index.php?rid=4886285&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01338.x</link>
            <description>Conclusion:  The method is valid for accurate quantification of Hb at a wide concentration range (&amp;gt;0.1 μm/L) in erythroid precursors or plasma and is optional for other biological fluids. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4886285</comments>
            <pubDate>Tue, 31 May 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4886285</guid>        </item>
        <item>
            <title>Increased numbers of circulating ECs are associated with systemic GVHD</title>
            <link>http://www.medworm.com/index.php?rid=4854972&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01322.x</link>
            <description>Conclusion:  Circulating ECs might be associated with systemic aGVHD. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4854972</comments>
            <pubDate>Tue, 24 May 2011 17:35:32 +0100</pubDate>
            <guid isPermaLink="false">4854972</guid>        </item>
        <item>
            <title>Influence of using a roller mixer on rejected samples in coagulation tests</title>
            <link>http://www.medworm.com/index.php?rid=4832671&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01334.x</link>
            <description>Conclusion:  We suggested using roller mixer to improve the reliability of coagulation testing. Such standardization in preanalytical phase may be helpful in preventing laboratory errors and obtaining correct test results in coagulation tests. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4832671</comments>
            <pubDate>Wed, 18 May 2011 18:39:50 +0100</pubDate>
            <guid isPermaLink="false">4832671</guid>        </item>
        <item>
            <title>Inappropriate use of protein C, protein S, and antithrombin testing for hereditary thrombophilia screening: an experience from a large university hospital</title>
            <link>http://www.medworm.com/index.php?rid=4832673&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01332.x</link>
            <description>Conclusion:  To enhance the appropriate use of hereditary thrombophilia screening tests, physician education concerning the patient selection, suitable timing for testing and repetition of the tests with abnormal results should be emphasized. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4832673</comments>
            <pubDate>Sun, 15 May 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4832673</guid>        </item>
        <item>
            <title>Factor VIIa‐Antithrombin complexes during cardiac surgery using cardiopulmonary bypass</title>
            <link>http://www.medworm.com/index.php?rid=4832672&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01331.x</link>
            <description>SummaryAntithrombin inhibits VIIa when bound to cellular tissue factor in the presence of heparin. VIIa concentrations increase within the surgical field during cardiopulmonary bypass surgery but decrease when measured in the patient. Using a new ELISA (Stago, Reading, UK), we measured VIIa–antithrombin complexes in patients undergoing cardiopulmonary bypass to determine whether antithrombin plays a physiological role in VIIa inhibition during cardiac surgery. Samples were taken from 13 adult patients undergoing cardiac surgery with cardiopulmonary bypass at the following time points: presurgery, postheparin, 20 min intervals during cardiopulmonary bypass and postprotamine. The presurgery concentrations of VIIa–antithrombin complexes were median of 52.7pm, and these rose postheparin ...</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4832672</comments>
            <pubDate>Sun, 15 May 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4832672</guid>        </item>
        <item>
            <title>Impact of sample volume and handling time during analysis on the in vitro quality measurements of platelet concentrates held in syringes</title>
            <link>http://www.medworm.com/index.php?rid=4790762&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01327.x</link>
            <description>Conclusion:  Sampling for pO2 determination should be carried out in small volumes and assessed within 30 min of collection to obtain reliable and comparable results. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4790762</comments>
            <pubDate>Fri, 06 May 2011 17:24:48 +0100</pubDate>
            <guid isPermaLink="false">4790762</guid>        </item>
        <item>
            <title>An evaluation of the Sebia capillarys Neonat Haemoglobin FAST™ system for routine newborn screening for sickle cell disease</title>
            <link>http://www.medworm.com/index.php?rid=4776544&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01315.x</link>
            <description>SummaryThe West Midlands Newborn Screening Laboratory (NBSL) at Birmingham Children’s Hospital (BCH), UK, screens approximately 71 000 babies per annum using the Bio‐Rad automated VARIANT™ nbs (Vnbs) high‐pressure liquid chromatograph (HPLC). Any abnormal haemoglobins detected, including S, C, D‐Punjab, E and O‐Arab as directed by the NHS Sickle Cell and Thalassaemia Screening Programme (NHS Sickle Cell and Thalassaemia Screening Programme Website, http://sct.screening.nhs.uk), are then confirmed using Resolve® isoelectric electric focusing (IEF) kits supplied by Perkin‐Elmer. The Sebia capillarys Neonat Haemoglobin FAST™ system was evaluated as a possible replacement for the first‐ or second‐line methods used. Both the Sebia and Bio‐Rad methods were compared using...</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4776544</comments>
            <pubDate>Tue, 03 May 2011 16:55:03 +0100</pubDate>
            <guid isPermaLink="false">4776544</guid>        </item>
        <item>
            <title>Clinical multicenter evaluation of a new FXa‐based Antithrombin assay</title>
            <link>http://www.medworm.com/index.php?rid=4776545&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01326.x</link>
            <description>Conclusion:  The INNOVANCE Antithrombin assay has high sensitivity for Antithrombin deficiencies and is reliable, precise and suitable for routine clinical use. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4776545</comments>
            <pubDate>Mon, 02 May 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4776545</guid>        </item>
        <item>
            <title>Molecular characterization of glucose‐6‐phosphate dehydrogenase deficiency in Pakistani population</title>
            <link>http://www.medworm.com/index.php?rid=4736805&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01325.x</link>
            <description>Conclusion:  We concluded that 563C‐T was the commonest G6PD variant, while 1003A‐G and 131C‐G were less‐frequent genetic variants of G6PD in Pakistani population. A novel genetic variant 973G‐A was also identified. Very low levels of G6PD enzyme activity was seen with G6PD 563C‐T. Mutational analysis failed in a significant proportion of samples warranting further work. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4736805</comments>
            <pubDate>Fri, 22 Apr 2011 17:22:04 +0100</pubDate>
            <guid isPermaLink="false">4736805</guid>        </item>
        <item>
            <title>Modification to reporting of qualitative fluorescent spot test results improves detection of glucose‐6‐phosphate dehydrogenase (G6PD)‐deficient heterozygote female newborns</title>
            <link>http://www.medworm.com/index.php?rid=4726542&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01309.x</link>
            <description>Conclusion:  Glucose‐6‐phosphate dehydrogenase heterozygote females cannot be identified by FST if fluorescence is reported as absent or present. Distinguishing samples with intermediate fluorescence from absent and bright fluorescence improves detection of heterozygote females with mild G6PD deficiency. Mutational studies confirmed that 85% of intermediate samples with normal enzyme activity had identifiable G6PD mutations. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4726542</comments>
            <pubDate>Tue, 19 Apr 2011 17:36:45 +0100</pubDate>
            <guid isPermaLink="false">4726542</guid>        </item>
        <item>
            <title>Ex vivo amplification of human hematopoietic stem and progenitor cells in an alginate three‐dimensional culture system</title>
            <link>http://www.medworm.com/index.php?rid=4716047&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01324.x</link>
            <description>Conclusion:  This study demonstrates a new and efficient method to amplify the CD34+ human cord blood hematopoietic stem/progenitor cells in a 3D alginate culture system ex vivo for extended periods while retaining the hematopoietic reconstruction capacity. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4716047</comments>
            <pubDate>Fri, 15 Apr 2011 18:37:21 +0100</pubDate>
            <guid isPermaLink="false">4716047</guid>        </item>
        <item>
            <title>The immunophenotypic stability of plasma cell myeloma by flow cytometry</title>
            <link>http://www.medworm.com/index.php?rid=4687231&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01317.x</link>
            <description>Conclusion:  Approximately 1/3 of PCM cases show IP changes over time, with CD45 the least stable antigen. Recognition of this relative instability is important to avoid narrow targeting of follow‐up FC analyses, especially for minimal residual disease monitoring. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4687231</comments>
            <pubDate>Wed, 06 Apr 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4687231</guid>        </item>
        <item>
            <title>Homozygous Hb Stanleyville‐II [alpha2 78(EF7) Asn&gt;Lys; HBA2:c.237C&gt;A, not C&gt;G] associated with genotype −α3.7/−α3.7 in two Brazilian families</title>
            <link>http://www.medworm.com/index.php?rid=4687230&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01321.x</link>
            <description>Conclusion:  Stanleyville‐II gene mutation is HBA2:c.237C&amp;gt;A, or C&amp;gt;G, and this information on the Globin Gene Server should be updated; AfeI test is a fast and accurate method to detect it; NBS programs should consider the possibility of Hb Stanleyville‐II whenever IEF shows one band in the HbS position, and another one between S and C. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4687230</comments>
            <pubDate>Wed, 06 Apr 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4687230</guid>        </item>
        <item>
            <title>Purging efficacy of ZnPcH1‐based photodynamic therapy on chronic myeloid leukemia bone marrow</title>
            <link>http://www.medworm.com/index.php?rid=4672253&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01313.x</link>
            <description>Conclusion:  Our data suggest that ZnPcH1‐PDT may be a useful modality for purging CML cells for autologous grafts. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4672253</comments>
            <pubDate>Sun, 03 Apr 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4672253</guid>        </item>
        <item>
            <title>Limitation of malaria diagnosis with the Cell‐Dyn® analyser: not all haemozoin‐containing monocytes are detected or shown</title>
            <link>http://www.medworm.com/index.php?rid=4672252&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01318.x</link>
            <description>(Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4672252</comments>
            <pubDate>Sun, 03 Apr 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4672252</guid>        </item>
        <item>
            <title>Correlation of assessment of plasma cells by flow cytometry and detection of cytogenomic abnormalities by fluorescence in situ hybridization in plasma cell neoplasms</title>
            <link>http://www.medworm.com/index.php?rid=4687229&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01323.x</link>
            <description>Conclusion:  In PCN cases, an FC‐assessed 3% PCC in BM aspirates should not be used as a cut‐off for further FISH testing. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4687229</comments>
            <pubDate>Thu, 31 Mar 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4687229</guid>        </item>
        <item>
            <title>Interleukin‐10 gene polymorphism reflects the severity of chronic immune thrombocytopenia in Japanese patients</title>
            <link>http://www.medworm.com/index.php?rid=4677919&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01320.x</link>
            <description>Conclusion:  According to our data, patients with low producer type of IL‐10 polymorphisms have more severe thrombocytopenia, suggesting that IL‐10 gene polymorphisms may reflect the severity of ITP. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4677919</comments>
            <pubDate>Thu, 31 Mar 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4677919</guid>        </item>
        <item>
            <title>Screening for CRLF2 overexpression in adult acute lymphoblastic leukemia</title>
            <link>http://www.medworm.com/index.php?rid=4672250&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01319.x</link>
            <description>(Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4672250</comments>
            <pubDate>Thu, 31 Mar 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4672250</guid>        </item>
        <item>
            <title>Kinetics of pDCs, mDCs, γδT cells and regulatory T cells in association with graft versus host disease after hematopoietic stem cell transplantation</title>
            <link>http://www.medworm.com/index.php?rid=4645497&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01300.x</link>
            <description>Conclusion:  The present study revealed an association of pDCs, mDCs, γδT cells and Treg cells with induction or treatment of GVHD. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4645497</comments>
            <pubDate>Tue, 29 Mar 2011 16:57:22 +0100</pubDate>
            <guid isPermaLink="false">4645497</guid>        </item>
        <item>
            <title>The first use of EaeI restriction enzyme in DNA diagnosis of Hb Q‐India</title>
            <link>http://www.medworm.com/index.php?rid=4632722&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01316.x</link>
            <description>Conclusion: EaeI restriction enzyme digestion can be used as a simple and robust alternative method to ARMS‐PCR for DNA diagnosis of Hb Q‐India. The EaeI restriction enzyme can be added to the panel of restriction enzymes used in the DNA diagnosis of the abnormal Hb variants. Concomitant use of HPLC and IEF can be used efficiently for presumed diagnosis of this rare variant. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4632722</comments>
            <pubDate>Fri, 25 Mar 2011 17:51:29 +0100</pubDate>
            <guid isPermaLink="false">4632722</guid>        </item>
        <item>
            <title>IgM interference in determination of antiphospholipid antibodies and erythrocyte sedimentation rate in persistent polyclonal B‐cell lymphocytosis with binucleated lymphocytes</title>
            <link>http://www.medworm.com/index.php?rid=4632725&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01310.x</link>
            <description>(Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4632725</comments>
            <pubDate>Thu, 24 Mar 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4632725</guid>        </item>
        <item>
            <title>A routine silica‐based activated partial thromboplastin time (Hemosil aPTT‐SP™) mostly excludes the presence of lupus anticoagulant</title>
            <link>http://www.medworm.com/index.php?rid=4632724&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01314.x</link>
            <description>(Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4632724</comments>
            <pubDate>Thu, 24 Mar 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4632724</guid>        </item>
        <item>
            <title>Prevalence of overt myeloproliferative neoplasms and JAK2 V617F mutation in Korean patients with splanchnic vein thrombosis</title>
            <link>http://www.medworm.com/index.php?rid=4632723&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01308.x</link>
            <description>Conclusion:  The prevalence of overt MPN and that of JAK2 V617F were lower in Korean patients with SVT than in previous reports. Data from a larger number of patients with long‐term follow‐up are needed to reveal the clinical relevancy of JAK2 V617F in Korean patients with SVT. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4632723</comments>
            <pubDate>Thu, 24 Mar 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4632723</guid>        </item>
        <item>
            <title>Erythrophagocytosis by neutrophils – a rare morphological phenomenon resulting in acquired haemolytic anaemia?</title>
            <link>http://www.medworm.com/index.php?rid=4617330&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01312.x</link>
            <description>We describe a female patient who presented with acquired haemolytic anaemia. Erythrophagocytosis was found in around 35% of neutrophils of the peripheral blood. A similar picture was seen in the bone marrow, but with additional erythrophagocytosis by macrophages. These two processes were considered as the main causes of anaemia, but the first one seemed to be predominant. Malignancies, autoimmunisation disorders and infections were excluded. Immunosuppressive therapy with corticosteroids was implemented, but had to be stopped because of side effects. Long‐term normalization of peripheral blood morphology was achieved after splenectomy. Splenectomy may be considered a therapeutic option for patients with diagnosed neutrophil erythrophagocytic hyperactivity. Therapy with corticosteroids is...</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4617330</comments>
            <pubDate>Tue, 22 Mar 2011 17:49:57 +0100</pubDate>
            <guid isPermaLink="false">4617330</guid>        </item>
        <item>
            <title>Optimization of laboratory workflow in clinical hematology laboratory with reduced manual slide review: comparison between Sysmex XE‐2100 and ABX Pentra DX120</title>
            <link>http://www.medworm.com/index.php?rid=4617332&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01306.x</link>
            <description>Conclusion:  Our data show that the slide‐making rates are variable in different hematology analyzers. It also implies that although MSR cannot be fully substituted by modern hematology analyzers, it can be effectively reduced to optimize laboratory workload. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4617332</comments>
            <pubDate>Mon, 21 Mar 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4617332</guid>        </item>
        <item>
            <title>Marked discrepancy between coagulometric Protein C activity assays with the pro‐thrombotic Protein C Asn2Ile substitution</title>
            <link>http://www.medworm.com/index.php?rid=4617331&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01311.x</link>
            <description>Conclusion:  We demonstrate that coagulometric assays are not equally sensitive to clinically important functional defects of PC and that multiple assays may be required to identify all variants. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4617331</comments>
            <pubDate>Mon, 21 Mar 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4617331</guid>        </item>
        <item>
            <title>Transillumination: a new tool to eliminate the impact of venous stasis during the procedure for the collection of diagnostic blood specimens for routine haematological testing</title>
            <link>http://www.medworm.com/index.php?rid=4607137&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01305.x</link>
            <description>Conclusion:  As such, considering that inappropriate use of the tourniquet is commonplace, we conclude that transillumination devices can represent a suitable tool to eliminate the venous stasis and to improve the quality of phlebotomy procedures. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4607137</comments>
            <pubDate>Fri, 18 Mar 2011 17:25:07 +0100</pubDate>
            <guid isPermaLink="false">4607137</guid>        </item>
        <item>
            <title>The phenotypic and genetic assessment of antithrombin deficiency</title>
            <link>http://www.medworm.com/index.php?rid=4596476&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01307.x</link>
            <description>Conclusion:  AT activity assays are essential for the detection of AT deficiency because type II defects are relatively common in patients with heritable deficiency. No one functional assay can be assumed to detect all forms of AT deficiency, and assays can sometimes be improved by reducing reaction time of AT with thrombin or factor Xa. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4596476</comments>
            <pubDate>Wed, 16 Mar 2011 17:33:27 +0100</pubDate>
            <guid isPermaLink="false">4596476</guid>        </item>
        <item>
            <title>Laboratory‐based ROTEM® analysis: implementing pneumatic tube transport and real‐time graphic transmission</title>
            <link>http://www.medworm.com/index.php?rid=4562204&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01303.x</link>
            <description>Conclusion:  At our institution, transport of blood samples by pneumatic delivery does not influence ROTEM® parameters. Blood samples can be analysed centrally, and results transmitted live via virtual network computing to emergency or operating rooms. Prior to analyse blood samples centrally, the type of sample transport should be tested to exclude in vitro blood activation by local pneumatic transport system. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4562204</comments>
            <pubDate>Wed, 09 Mar 2011 17:25:12 +0100</pubDate>
            <guid isPermaLink="false">4562204</guid>        </item>
        <item>
            <title>ICSH review of the measurement of the erythocyte sedimentation rate</title>
            <link>http://www.medworm.com/index.php?rid=4518595&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01302.x</link>
            <description>SummaryIn recognition of the need for a standardization of the measurement of the erythrocyte sedimentation rate (ESR), the International Council for Standardization in Haematology makes the following recommendations: (i) The reference method for measurement of the ESR should be based on the Westergren method, which is a specific test for the ESR, with modifications, (ii) The reference method for measurement of the ESR should use either whole blood anticoagulated with EDTA and later diluted with sodium citrate or saline (4 : 1) or whole blood anticoagulated with sodium citrate (4 : 1) in Westergren pipettes, (iii) The ESR pipettes can be of glass or plastic (with specific characteristics). It must be colourless; a minimum sedimentation scale of 200 mm, a minimum bore of 2.55 mm...</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4518595</comments>
            <pubDate>Fri, 25 Feb 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4518595</guid>        </item>
        <item>
            <title>An assessment of three noncommercial DNA extraction methods from dried blood spots for beta‐thalassaemia mutation identification</title>
            <link>http://www.medworm.com/index.php?rid=4518594&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01304.x</link>
            <description>Conclusion:  The NaOH method is a simple method that uses minimal equipment and reagents that make it labour‐ and cost‐effective. This method could be adopted by poorer countries to extract DNA for beta‐thalassaemia mutation characterization. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4518594</comments>
            <pubDate>Fri, 25 Feb 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4518594</guid>        </item>
        <item>
            <title>Screening of sepsis using leukocyte cell population data from the Coulter automatic blood cell analyzer DxH800</title>
            <link>http://www.medworm.com/index.php?rid=4503214&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01298.x</link>
            <description>Conclusion:  Many of the leukocyte CPD have been identified as useful parameters of sepsis. Hopefully, these parameters can ultimately be incorporated into a decision rule for the screening of sepsis samples and to discriminate fungemia from bacteremia. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4503214</comments>
            <pubDate>Tue, 22 Feb 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4503214</guid>        </item>
        <item>
            <title>Megaloblastic pancytopenia vis‐à‐vis non‐megaloblastic pancytopenia: is mean platelet volume useful discriminating indicator</title>
            <link>http://www.medworm.com/index.php?rid=4461184&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01296.x</link>
            <description>Conclusion:  MPV has limited sensitivity and specificity to discriminate between megaloblastic and non‐megaloblastic pancytopenia. Pancytopenia due to aplastic/hypocellular marrow and acute leukaemia has significantly lower MPV than megaloblastic group while other pancytopenic cases do not show any statistical difference in MPV from megaloblastic pancytopenia. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4461184</comments>
            <pubDate>Thu, 10 Feb 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4461184</guid>        </item>
        <item>
            <title>Distinctive hematological abnormalities in East Asian neonates and children with down syndrome</title>
            <link>http://www.medworm.com/index.php?rid=4518593&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01299.x</link>
            <description>Conclusion:  East Asian DS neonates and children showed distinctive spectrum of hematological abnormalities. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4518593</comments>
            <pubDate>Tue, 01 Feb 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4518593</guid>        </item>
        <item>
            <title>Presumptive diagnosis of common haemoglobinopathies in Southeast Asia using a capillary electrophoresis system</title>
            <link>http://www.medworm.com/index.php?rid=4503213&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01301.x</link>
            <description>Conclusion:  The capillary electrophoresis system could clearly demonstrate the presence of abnormal Hbs and provide useful information for presumptive diagnoses in most cases. The Hb analysis results could help in selection of appropriate DNA testing for final diagnoses of these variants. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4503213</comments>
            <pubDate>Tue, 01 Feb 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4503213</guid>        </item>
        <item>
            <title>Pro‐oxidative/antioxidative imbalance: a key indicator of adverse outcome in hematopoietic stem cell transplantation</title>
            <link>http://www.medworm.com/index.php?rid=4461183&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2011.01297.x</link>
            <description>Conclusion:  Pretransplantation IO might be a major contributor to adverse outcome in HSCT recipients through an impaired pro‐oxidative/antioxidative homeostasis. The reversible nature of IO and oxidative stress suggests that early preventive strategies might have a potential to improve transplant outcome. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4461183</comments>
            <pubDate>Tue, 01 Feb 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4461183</guid>        </item>
        <item>
            <title>Evaluation of schistocyte monitoring after haematopoietic stem cell transplantation</title>
            <link>http://www.medworm.com/index.php?rid=4425479&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2010.01292.x</link>
            <description>Conclusion:  In our experience, systematic schistocyte count after HSCT proved to be useful: the occurrence of an increased percentage was a surrogate marker for complications even if unspecific for TM. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4425479</comments>
            <pubDate>Tue, 01 Feb 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4425479</guid>        </item>
        <item>
            <title>Various patterns of IgH deletion identified by FISH using combined IgH and IgH/CCND1 probes in multiple myeloma and chronic lymphocytic leukemia</title>
            <link>http://www.medworm.com/index.php?rid=4407370&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2010.01290.x</link>
            <description>Conclusion:  A variety of patterns of the IgH deletion were identified by interphase FISH using IgH break‐apart and IgH/CCND1 probes in patients with MM and CLL. The results of this study suggest that the integrated information obtained with IgH break‐apart and IgH/CCND1 FISH was needed to interpret FISH results unambiguously. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4407370</comments>
            <pubDate>Fri, 28 Jan 2011 16:23:57 +0100</pubDate>
            <guid isPermaLink="false">4407370</guid>        </item>
        <item>
            <title>Haemoglobin (Hb) G‐Philadelphia, Hb Stanleyville‐II, Hb G‐Norfolk, Hb Matsue‐Oki and Hb Mizushi can form a panel of α‐chain variants that overlap in their phenotype: the novel use of StyI to screen for Hb G‐Philadelphia</title>
            <link>http://www.medworm.com/index.php?rid=4401452&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2010.01289.x</link>
            <description>Conclusion:  A novel StyI restriction enzyme can be used to confirm the commonest type of Hb G‐Philadelphia. DNA sequencing identified four other α‐chain variants with a similar HPLC and IEF phenotype. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4401452</comments>
            <pubDate>Thu, 27 Jan 2011 16:18:36 +0100</pubDate>
            <guid isPermaLink="false">4401452</guid>        </item>
        <item>
            <title>Three novel alternative splicing mutations in BCR‐ABL1 detected in CML patients with resistance to kinase inhibitors</title>
            <link>http://www.medworm.com/index.php?rid=4401454&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2010.01291.x</link>
            <description>Conclusion:  These findings, when combined with the data on 35INS, support the concept that loss of the C‐terminus of BCR‐ABL1 is associated with significant resistance to kinase inhibitors; this mechanism appears to be a major source of resistance to kinase inhibitors. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4401454</comments>
            <pubDate>Wed, 26 Jan 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4401454</guid>        </item>
        <item>
            <title>Performance evaluation of the Celltac F haematology analyser</title>
            <link>http://www.medworm.com/index.php?rid=4401453&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2010.01294.x</link>
            <description>Conclusion:  The Celltac F shows broadly comparable analytical performance to the XE‐2100 for the parameters assessed. The Celltac F is recommendable for medium‐sized laboratories or as a back‐up instrument in larger laboratories. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4401453</comments>
            <pubDate>Wed, 26 Jan 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4401453</guid>        </item>
        <item>
            <title>Usefulness of thyrogastric immune features as predictors of pernicious anaemia that lacks intrinsic factor antibody</title>
            <link>http://www.medworm.com/index.php?rid=4373798&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2010.01295.x</link>
            <description>Conclusion:  Patients with two out of three features, GPC, antithyroid antibodies, gastric atrophy, but without HP organisms; or three features with HP organisms, can be predicted to have PA. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4373798</comments>
            <pubDate>Thu, 20 Jan 2011 16:12:48 +0100</pubDate>
            <guid isPermaLink="false">4373798</guid>        </item>
        <item>
            <title>CIP2A is over‐expressed in acute myeloid leukaemia and associated with HL60 cells proliferation and differentiation</title>
            <link>http://www.medworm.com/index.php?rid=4332823&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2010.01288.x</link>
            <description>Conclusions:  These results suggest that CIP2A is over‐expressed in patients with newly diagnosed/relapsed AML and the expression of CIP2A could have potential use as a clinical marker for AML relapse after treatment. The high expression of CIP2A in HL60 cells may be related to active cell proliferation and arrest of cell differentiation. This study may shed light on the molecular function of CIP2A in myeloid leukemogenesis. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4332823</comments>
            <pubDate>Wed, 12 Jan 2011 16:40:48 +0100</pubDate>
            <guid isPermaLink="false">4332823</guid>        </item>
        <item>
            <title>The assessment of aspirin resistance by using light transmission and multiple electrode aggregometry</title>
            <link>http://www.medworm.com/index.php?rid=4332825&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2010.01286.x</link>
            <description>Conclusion:  If ASA resistance is detected by laboratory tests, replacement of ASA or its combination with other antiplatelet drugs as well as increased dosage may be considered. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4332825</comments>
            <pubDate>Tue, 11 Jan 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4332825</guid>        </item>
        <item>
            <title>The importance of β globin deletion analysis in the evaluation of patients with β thalassemia</title>
            <link>http://www.medworm.com/index.php?rid=4332824&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2010.01287.x</link>
            <description>Conclusion:  Beta globin deletion/duplication analysis is necessary to correctly identify the genotype in some patients being evaluated for beta thalassemia. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4332824</comments>
            <pubDate>Tue, 11 Jan 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4332824</guid>        </item>
        <item>
            <title>List of Reviewers</title>
            <link>http://www.medworm.com/index.php?rid=4327759&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2010.01293.x</link>
            <description>(Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4327759</comments>
            <pubDate>Mon, 10 Jan 2011 15:06:18 +0100</pubDate>
            <guid isPermaLink="false">4327759</guid>        </item>
        <item>
            <title>Letter to the Editor</title>
            <link>http://www.medworm.com/index.php?rid=4327758&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2010.01226.x</link>
            <description>(Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4327758</comments>
            <pubDate>Mon, 10 Jan 2011 15:06:14 +0100</pubDate>
            <guid isPermaLink="false">4327758</guid>        </item>
        <item>
            <title>Biologic characteristics of bone marrow–derived mesenchymal stem cells from a patient with thalassemia syndrome</title>
            <link>http://www.medworm.com/index.php?rid=4296766&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2010.01285.x</link>
            <description>Conclusion:  T‐MSCs exhibited normal phenotype, karyotype as well as normal immunomodulatory function, and autologous MSCs from patients with thalassemia syndrome may be an attractive source of stem cell in terms of hematopoietic support as well as immunomodulatory activity. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4296766</comments>
            <pubDate>Wed, 29 Dec 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4296766</guid>        </item>
        <item>
            <title>Comparison of array comparative genomic hybridization (aCGH) to FISH and cytogenetics in prognostic evaluation of chronic lymphocytic leukemia</title>
            <link>http://www.medworm.com/index.php?rid=4246774&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2010.01284.x</link>
            <description>Discussion:  Our findings suggest aCGH is an effective technique for evaluating recurring genetic abnormalities in CLL and improves on standard FISH in detecting genetic abnormalities in CLL. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4246774</comments>
            <pubDate>Thu, 09 Dec 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4246774</guid>        </item>
        <item>
            <title>Myeloperoxidase as a diagnostic and prognostic marker in cardiology: beware of pre‐analytical factors that may influence results</title>
            <link>http://www.medworm.com/index.php?rid=4221524&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2010.01281.x</link>
            <description>(Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4221524</comments>
            <pubDate>Wed, 01 Dec 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4221524</guid>        </item>
        <item>
            <title>The diagnostic utility of bone marrow biopsies performed for the investigation of fever and/or cytopenias in HIV‐infected adults at Groote Schuur Hospital, Western Cape, South Africa</title>
            <link>http://www.medworm.com/index.php?rid=4215692&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2010.01280.x</link>
            <description>Conclusion:  In our study group, a bone marrow biopsy was a useful investigation with a high diagnostic yield. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4215692</comments>
            <pubDate>Wed, 01 Dec 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4215692</guid>        </item>
        <item>
            <title>JAK2V617F mutation in patients with thrombosis: to screen or not to screen?</title>
            <link>http://www.medworm.com/index.php?rid=4215691&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2010.01275.x</link>
            <description>Conclusion:  Routine testing for JAK2V617F is not currently recommended for patients with unexplained thromboses, except for those with splanchnic vein thrombosis. In patients with cerebral vein thrombosis, the value of testing for JAK2V617F mutation is yet to be established. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4215691</comments>
            <pubDate>Wed, 01 Dec 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4215691</guid>        </item>
        <item>
            <title>Heparin‐induced thrombocytopenia: evaluation of IgG and IgGAM ELISA assays</title>
            <link>http://www.medworm.com/index.php?rid=4215690&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2010.01276.x</link>
            <description>Conclusion:  Our data strongly support the use of IgG‐only assays for the detection of HIT antibodies. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4215690</comments>
            <pubDate>Wed, 01 Dec 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4215690</guid>        </item>
        <item>
            <title>A novel approach for assessments of erythrocyte sedimentation rate</title>
            <link>http://www.medworm.com/index.php?rid=4215689&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2010.01277.x</link>
            <description>Conclusion:  Thus, unlike Westergren erythrocyte sedimentation rate, sedimentation data obtained by the proposed method do not require correction for Hct. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4215689</comments>
            <pubDate>Wed, 01 Dec 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4215689</guid>        </item>
        <item>
            <title>Anticoagulation services in Malta – an economic study comparing a central laboratory model vs. a point‐of‐care approach</title>
            <link>http://www.medworm.com/index.php?rid=4215688&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2010.01279.x</link>
            <description>(Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4215688</comments>
            <pubDate>Wed, 01 Dec 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4215688</guid>        </item>
        <item>
            <title>Rapid identification of hemoglobin Quong Sze mutation using high‐resolution melting analysis</title>
            <link>http://www.medworm.com/index.php?rid=4215687&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2010.01278.x</link>
            <description>(Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4215687</comments>
            <pubDate>Wed, 01 Dec 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4215687</guid>        </item>
        <item>
            <title>Letter to the Editor</title>
            <link>http://www.medworm.com/index.php?rid=4215686&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2010.01281.x</link>
            <description>(Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4215686</comments>
            <pubDate>Wed, 01 Dec 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4215686</guid>        </item>
        <item>
            <title>BsaXI/RFLP analysis of initial or selectively reamplified PCR product is unreliable in detecting the V617F mutation in JAK2</title>
            <link>http://www.medworm.com/index.php?rid=4215685&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2010.01282.x</link>
            <description>Conclusion:  This combination of problems effectively combines to render selective reamplification and redigestion unsuitable for detecting low fractions of the V617F mutation. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4215685</comments>
            <pubDate>Wed, 01 Dec 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4215685</guid>        </item>
        <item>
            <title>Evaluation of activated partial thromboplastin time (aPTT) reagents for application in biomedical diagnostic device development</title>
            <link>http://www.medworm.com/index.php?rid=4215684&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2010.01283.x</link>
            <description>Conclusion:  Two reagents, namely aPTT‐SP and SynthASIL both of which are based on synthetic phospholipids and silica, were identified as promising candidates for incorporation into point‐of‐care diagnostic device platforms as dried reagents. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4215684</comments>
            <pubDate>Wed, 01 Dec 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4215684</guid>        </item>
        <item>
            <title>Nonsense mutation of β‐globin gene at codon 82 (AAG→TAG) or HBB:C247 A→T with polymorphism: cause of thalassemia intermedia?</title>
            <link>http://www.medworm.com/index.php?rid=4135979&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2010.01273.x</link>
            <description>(Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4135979</comments>
            <pubDate>Fri, 05 Nov 2010 19:55:49 +0100</pubDate>
            <guid isPermaLink="false">4135979</guid>        </item>
        <item>
            <title>A case of Plasmodium vivax with unusual enlarged gametocytes</title>
            <link>http://www.medworm.com/index.php?rid=4135980&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2010.01272.x</link>
            <description>(Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4135980</comments>
            <pubDate>Thu, 04 Nov 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4135980</guid>        </item>
        <item>
            <title>Cryoglobulin detection from blood and peritoneal fluid smears</title>
            <link>http://www.medworm.com/index.php?rid=4135983&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2010.01269.x</link>
            <description>SummaryLaboratory identification of cytoplasmic inclusions in leucocytes as unusual manifestation of cryoglobulinemia has been previously reported (Maitra et al., 2000 American Journal of Clinical Pathology, 113, 107–112; Fohlen‐Walter et al., 2002American Journal of Clinical Pathology, 117, 606–614.). We would like to add two observations highlighting the following: (i) the peculiar picture of cryoglobulins in neutrophils and monocytes but sparing other white blood cell (WBC) and (ii) possibility of deposit occurrence with morphological identification in body fluids. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4135983</comments>
            <pubDate>Wed, 03 Nov 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4135983</guid>        </item>
        <item>
            <title>Detection of hereditary pyropoikilocytosis by the eosin‐5‐maleimide (EMA)‐binding test is attributable to a marked reduction in EMA‐reactive transmembrane proteins</title>
            <link>http://www.medworm.com/index.php?rid=4135982&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2010.01270.x</link>
            <description>Conclusion:  Lesser amounts of EMA‐reactive membrane proteins were detected in HPP than HS red cells, thus confirming their lower fluorescence readings in the EMA‐binding test. The concomitant reduction in glycophorins A and C, and CD59 in HPP could have caused cellular contraction, resulting in poikilocytosis. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4135982</comments>
            <pubDate>Wed, 03 Nov 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4135982</guid>        </item>
        <item>
            <title>Resistance to aspirin and clopidogrel therapy</title>
            <link>http://www.medworm.com/index.php?rid=4135981&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2010.01268.x</link>
            <description>Conclusion:  Data from ongoing and future studies are awaited to better understand this entity and to highlight the most appropriate treatment strategies. (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4135981</comments>
            <pubDate>Wed, 03 Nov 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4135981</guid>        </item>
        <item>
            <title>Comparison between siliconized evacuated glass and plastic blood collection tubes for prothrombin time and activated partial thromboplastin time assay in normal patients, patients on oral anticoagulant therapy and patients with unfractioned heparin therapy</title>
            <link>http://www.medworm.com/index.php?rid=4110887&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2010.01271.x</link>
            <description>Summary (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4110887</comments>
            <pubDate>Fri, 29 Oct 2010 18:22:23 +0100</pubDate>
            <guid isPermaLink="false">4110887</guid>        </item>
        <item>
            <title>MFI ratio estimation of ZAP‐70 in B‐CLL by flow cytometry can be improved by considering the isotype‐matched antibody signal</title>
            <link>http://www.medworm.com/index.php?rid=4041932&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2010.01263.x</link>
            <description>Summary (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4041932</comments>
            <pubDate>Thu, 30 Sep 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4041932</guid>        </item>
        <item>
            <title>An investigation of reversal of imatinib resistance in the Bcr‐Abl positive imatinib‐resistant cell line K562r by dasatinib, nilotinib, rapamycin and bortezomib</title>
            <link>http://www.medworm.com/index.php?rid=4033162&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2010.01267.x</link>
            <description>Summary (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4033162</comments>
            <pubDate>Thu, 30 Sep 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4033162</guid>        </item>
        <item>
            <title>The investigation of a prolonged APTT with specific clotting factor assays is unnecessary if an APTT with Actin FS is normal</title>
            <link>http://www.medworm.com/index.php?rid=4014959&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2010.01266.x</link>
            <description>Summary (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4014959</comments>
            <pubDate>Thu, 30 Sep 2010 14:53:53 +0100</pubDate>
            <guid isPermaLink="false">4014959</guid>        </item>
        <item>
            <title>Development of an algorithm of satellite markers for monitoring chimerism status in post‐allogeneic haematopoietic stem cell transplantation patients</title>
            <link>http://www.medworm.com/index.php?rid=4006076&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2010.01264.x</link>
            <description>Summary (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4006076</comments>
            <pubDate>Wed, 29 Sep 2010 14:24:12 +0100</pubDate>
            <guid isPermaLink="false">4006076</guid>        </item>
        <item>
            <title>Screening for lupus anticoagulant: improving the performance of the lupus‐sensitive PTT‐LA</title>
            <link>http://www.medworm.com/index.php?rid=3995646&amp;cid=s_29466_19_f&amp;fid=29466&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1751-553X.2010.01262.x</link>
            <description>Summary (Source: Clinical and Laboratory Haematology)</description>
            <author>Clinical and Laboratory Haematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3995646</comments>
            <pubDate>Fri, 24 Sep 2010 08:11:24 +0100</pubDate>
            <guid isPermaLink="false">3995646</guid>        </item>
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            <title>The responsiveness of different APTT reagents to mild factor VIII, IX and XI deficiencies</title>
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