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        <title>International Journal of Laboratory Hematology via MedWorm.com</title>
        <description>MedWorm.com provides a medical RSS filtering service. Over 6000 RSS medical sources are combined and output via different filters. This feed contains the latest items from the 'International Journal of Laboratory Hematology' source.</description>
        <link><![CDATA[http://www.medworm.com/rss/search.php?qu=International+Journal+of+Laboratory+Hematology&t=International+Journal+of+Laboratory+Hematology&s=Search&f=source]]></link>
        <lastBuildDate>Wed, 08 Feb 2012 17:42:03 +0100</lastBuildDate>
        <item>
            <title>List of reviewers.</title>
            <link>http://www.medworm.com/index.php?rid=5538493&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22188998%26dopt%3DAbstract</link>
            <description>Authors: 
    PMID: 22188998 [PubMed - in process] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5538493</comments>
            <pubDate>Sun, 25 Dec 2011 09:06:13 +0100</pubDate>
            <guid isPermaLink="false">5538493</guid>        </item>
        <item>
            <title>Association of Janus kinase 2 (JAK2) polymorphisms with acute leukemia susceptibility.</title>
            <link>http://www.medworm.com/index.php?rid=5538494&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22168550%26dopt%3DAbstract</link>
            <description>Conclusion:â€‚ The results indicate that the risk of acute leukemia might be associated with JAK2 polymorphisms.
    PMID: 22168550 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5538494</comments>
            <pubDate>Wed, 14 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5538494</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=5538495&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22151199%26dopt%3DAbstract</link>
            <description>Conclusions:â€‚ 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.
    PMID: 22151199 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5538495</comments>
            <pubDate>Thu, 08 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5538495</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=5496135&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22145750%26dopt%3DAbstract</link>
            <description>Conclusion:â€‚ Bortezomib is a promising potential therapy for acute leukemia, especially mdr1 drug-resistant leukemia.
    PMID: 22145750 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5496135</comments>
            <pubDate>Wed, 07 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5496135</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=5496134&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22145778%26dopt%3DAbstract</link>
            <description>Conclusions:â€‚ 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.
    PMID: 22145778 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5496134</comments>
            <pubDate>Wed, 07 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5496134</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=5496131&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22145801%26dopt%3DAbstract</link>
            <description>Conclusion:â€‚ A group of proteins associated with BC can be obtained and the result of this study might provide clues for further research.
    PMID: 22145801 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5496131</comments>
            <pubDate>Wed, 07 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5496131</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=5496136&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22122800%26dopt%3DAbstract</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.
    PMID: 22122800 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5496136</comments>
            <pubDate>Tue, 29 Nov 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5496136</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=5427935&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22085261%26dopt%3DAbstract</link>
            <description>Conclusion:â€‚ In this collective of subjectively healthy elderly individuals, monocyte anisocytosis, neutrophil anisocytosis and mean lymphocyte volume were associated with decreased HoloTC.
    PMID: 22085261 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5427935</comments>
            <pubDate>Wed, 16 Nov 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5427935</guid>        </item>
        <item>
            <title>ICSH recommendations for identification, diagnostic value, and quantitation of schistocytes.</title>
            <link>http://www.medworm.com/index.php?rid=5427936&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22081912%26dopt%3DAbstract</link>
            <description>Authors: Zini G, d'Onofrio G, Briggs C, Erber W, Jou JM, Lee SH, McFadden S, Vives-Corrons JL, Yutaka N, Lesesve JF
    Abstract
    Schistocytes 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 (IC...</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5427936</comments>
            <pubDate>Tue, 15 Nov 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5427936</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=5427937&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22078096%26dopt%3DAbstract</link>
            <description>Conclusion:â€‚ 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.
    PMID: 22078096 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5427937</comments>
            <pubDate>Mon, 14 Nov 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5427937</guid>        </item>
        <item>
            <title>Sensitive detection and accurate monitoring of Plasmodium vivax parasites on routine complete blood count using automatic blood cell analyzer (DxH800(TM) ).</title>
            <link>http://www.medworm.com/index.php?rid=5427938&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22074115%26dopt%3DAbstract</link>
            <description>Conclusion:â€‚ DxH800â„¢ provides very sensitive and specific, easily recognizable P.Â vivax malaria signals on routine CBC without need for the additional reagents or special procedures.
    PMID: 22074115 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5427938</comments>
            <pubDate>Fri, 11 Nov 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5427938</guid>        </item>
        <item>
            <title>Scanning electron microscopy analysis of erythrocytes in thromboembolic ischemic stroke.</title>
            <link>http://www.medworm.com/index.php?rid=5427939&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22067299%26dopt%3DAbstract</link>
            <description>Conclusion:â€‚ 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.
    PMID: 22067299 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5427939</comments>
            <pubDate>Wed, 09 Nov 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5427939</guid>        </item>
        <item>
            <title>Influence of in vitro hemolysis on hematological testing on Advia 2120.</title>
            <link>http://www.medworm.com/index.php?rid=5383295&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22051137%26dopt%3DAbstract</link>
            <description>Conclusion:â€‚ The results of routine hematological testing on mildly to frankly hemolyzed specimens might be unreliable.
    PMID: 22051137 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5383295</comments>
            <pubDate>Thu, 03 Nov 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5383295</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=5383298&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22032515%26dopt%3DAbstract</link>
            <description>Conclusion:â€‚ The combination of mixing and confirmatory tests interpreted according to the new guidelines can clearly differentiate LA from other coagulopathies.
    PMID: 22032515 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5383298</comments>
            <pubDate>Fri, 28 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5383298</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=5317096&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21985133%26dopt%3DAbstract</link>
            <description>Conclusion:â€‚ 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.
    PMID: 21985133 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5317096</comments>
            <pubDate>Mon, 10 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5317096</guid>        </item>
        <item>
            <title>ICSH recommendations for the measurement of Haemoglobin A(2).</title>
            <link>http://www.medworm.com/index.php?rid=5302012&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21974826%26dopt%3DAbstract</link>
            <description>Authors: Stephens AD, Angastiniotis M, Baysal E, Chan V, Fucharoen S, Giordano PC, Hoyer JD, Mosca A, Wild B, 
    Abstract
    Although DNA analysis is needed for characterization of the mutations that cause Î²-thalassaemia, measurement of the Hb A(2) is essential for the routine identification of people who are carriers of Î²-thalassaemia. The methods of quantitating Hb A(2) are described together with pitfalls in undertaking these laboratory tests with particular emphasis on automated high-performance liquid chromatography and capillary electrophoresis.
    PMID: 21974826 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5302012</comments>
            <pubDate>Wed, 05 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5302012</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=5195558&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21884505%26dopt%3DAbstract</link>
            <description>Conclusion:â€‚ 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.
    PMID: 21884505 [PubMed - in process] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5195558</comments>
            <pubDate>Tue, 06 Sep 2011 02:56:12 +0100</pubDate>
            <guid isPermaLink="false">5195558</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=5195563&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21883966%26dopt%3DAbstract</link>
            <description>Authors: Bench AJ
    Abstract
    The 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 mar...</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5195563</comments>
            <pubDate>Thu, 25 Aug 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5195563</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=5195559&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21883970%26dopt%3DAbstract</link>
            <description>Conclusion:â€‚ CE is the preferable method for screening of heterozygote and homozygote of Hb CS. Moreover, in conjunction with a lower MCV (&amp;lt;70â€ƒfL), this approach provided a high resolution to identify Hb H-CS disease.
    PMID: 21883970 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5195559</comments>
            <pubDate>Thu, 25 Aug 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5195559</guid>        </item>
        <item>
            <title>State of the art in myeloid sarcoma.</title>
            <link>http://www.medworm.com/index.php?rid=5195562&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21883967%26dopt%3DAbstract</link>
            <description>Conclusion:â€‚ 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.
    PMID: 21883967 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5195562</comments>
            <pubDate>Tue, 23 Aug 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5195562</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=5195561&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21883968%26dopt%3DAbstract</link>
            <description>Conclusion:â€‚ 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.
    PMID: 21883968 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5195561</comments>
            <pubDate>Tue, 23 Aug 2011 23:00:00 +0100</pubDate>
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        <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=5195560&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21883969%26dopt%3DAbstract</link>
            <description>Conclusion:â€‚ 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.
    PMID: 21883969 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5195560</comments>
            <pubDate>Tue, 23 Aug 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5195560</guid>        </item>
        <item>
            <title>A novel test tube method of screening for hemoglobin E.</title>
            <link>http://www.medworm.com/index.php?rid=5195564&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21883965%26dopt%3DAbstract</link>
            <description>Conclusion:â€‚ The described novel test tube method could be an alternative method of mass population screening for HbE, particularly in small health care facilities.
    PMID: 21883965 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5195564</comments>
            <pubDate>Mon, 22 Aug 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5195564</guid>        </item>
        <item>
            <title>Differentiating between intra- and extracellular chemiluminescence in diluted whole-blood samples.</title>
            <link>http://www.medworm.com/index.php?rid=5142751&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21834798%26dopt%3DAbstract</link>
            <description>Conclusion:â€‚ Measurement of Ca-I-activated CL enhanced with 10(-4) â€ƒm 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) â€ƒm isoluminol and with addition of HRP is recommended for the detection of extracellular CL.
    PMID: 21834798 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5142751</comments>
            <pubDate>Wed, 10 Aug 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5142751</guid>        </item>
        <item>
            <title>Using the laboratory to predict recurrent venous thrombosis.</title>
            <link>http://www.medworm.com/index.php?rid=4971558&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21692994%26dopt%3DAbstract</link>
            <description>Authors: Baglin T
    Characterisation 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 inaccurac...</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4971558</comments>
            <pubDate>Mon, 27 Jun 2011 22:31:10 +0100</pubDate>
            <guid isPermaLink="false">4971558</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=4971557&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21692995%26dopt%3DAbstract</link>
            <description>Conclusion:â€‚ East Asian DS neonates and children showed distinctive spectrum of hematological abnormalities.
    PMID: 21692995 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4971557</comments>
            <pubDate>Mon, 27 Jun 2011 22:31:00 +0100</pubDate>
            <guid isPermaLink="false">4971557</guid>        </item>
        <item>
            <title>Kinetics of pDCs, mDCs, Î³Î´T 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=4971556&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21692996%26dopt%3DAbstract</link>
            <description>Conclusion:â€‚ The present study revealed an association of pDCs, mDCs, Î³Î´T cells and Treg cells with induction or treatment of GVHD.
    PMID: 21692996 [PubMed - in process] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4971556</comments>
            <pubDate>Mon, 27 Jun 2011 22:30:45 +0100</pubDate>
            <guid isPermaLink="false">4971556</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=4971555&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21692997%26dopt%3DAbstract</link>
            <description>Authors: McCarron SL, Haslam K, Kelly J, Duggan C, Langabeer SE
    
    PMID: 21692997 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4971555</comments>
            <pubDate>Tue, 21 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4971555</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=4971554&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21692998%26dopt%3DAbstract</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 â‰¥70â€ƒyears 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 result and wer...</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4971554</comments>
            <pubDate>Tue, 21 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4971554</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=4971562&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21679309%26dopt%3DAbstract</link>
            <description>Conclusion:â€‚; 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.
    PMID: 21679309 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4971562</comments>
            <pubDate>Wed, 15 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4971562</guid>        </item>
        <item>
            <title>Assessment of antithrombin deficiency in the real world.</title>
            <link>http://www.medworm.com/index.php?rid=4971561&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21679310%26dopt%3DAbstract</link>
            <description>Authors: Cooper PC, Coath FL, Daly M, Makris M
    
    PMID: 21679310 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4971561</comments>
            <pubDate>Wed, 15 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4971561</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=4971560&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21679311%26dopt%3DAbstract</link>
            <description>Authors: Li WJ, Cui L, Gao C, Zhao XX, Liu SG, Xing YP, Zhang RD, Zhang DW, Wang B, Li ZG, Wu MY
    
    PMID: 21679311 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4971560</comments>
            <pubDate>Wed, 15 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4971560</guid>        </item>
        <item>
            <title>Accurate testing for dysfunctional molecules: the potential for missing the diagnosis.</title>
            <link>http://www.medworm.com/index.php?rid=4971559&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21679312%26dopt%3DAbstract</link>
            <description>Authors: Marlar RA
    
    PMID: 21679312 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4971559</comments>
            <pubDate>Wed, 15 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4971559</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=4971565&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21668655%26dopt%3DAbstract</link>
            <description>Conclusion:â€‚ 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.
    PMID: 21668655 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4971565</comments>
            <pubDate>Sun, 12 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4971565</guid>        </item>
        <item>
            <title>Assessment for antithrombin deficiency in the real world.</title>
            <link>http://www.medworm.com/index.php?rid=4971564&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21668656%26dopt%3DAbstract</link>
            <description>Authors: Favaloro EJ
    
    PMID: 21668656 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4971564</comments>
            <pubDate>Sun, 12 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4971564</guid>        </item>
        <item>
            <title>Genotyping of human platelet antigen-15 by single closed-tube T(m) -shift method.</title>
            <link>http://www.medworm.com/index.php?rid=4971563&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21668657%26dopt%3DAbstract</link>
            <description>Conclusion:â€‚ The single closed-tube T(m) -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.
    PMID: 21668657 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4971563</comments>
            <pubDate>Sun, 12 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4971563</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=4923055&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21645281%26dopt%3DAbstract</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(Â®) GENÂ·Sâ„¢ 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 3450â€ƒmg/dl, we observed that triglyceride level was 1466â€ƒmg/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 c...</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4923055</comments>
            <pubDate>Sun, 05 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4923055</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=4923054&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21645282%26dopt%3DAbstract</link>
            <description>Authors: Fujita H, Hamaki T, Ohwada A, Tomiyama J, Nishimura S
    
    PMID: 21645282 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4923054</comments>
            <pubDate>Sun, 05 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4923054</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=4923053&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21645283%26dopt%3DAbstract</link>
            <description>Authors: Saki N, Saki F, Saki MR, Karimi M
    
    PMID: 21645283 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4923053</comments>
            <pubDate>Sun, 05 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4923053</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=4923057&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21631891%26dopt%3DAbstract</link>
            <description>Conclusion:â€‚ 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.
    PMID: 21631891 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4923057</comments>
            <pubDate>Tue, 31 May 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4923057</guid>        </item>
        <item>
            <title>Precise quantification of haemoglobin in erythroid precursors and plasma.</title>
            <link>http://www.medworm.com/index.php?rid=4923056&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21631892%26dopt%3DAbstract</link>
            <description>Conclusion:â€‚ The method is valid for accurate quantification of Hb at a wide concentration range (&amp;gt;0.1â€ƒÎ¼m/L) in erythroid precursors or plasma and is optional for other biological fluids.
    PMID: 21631892 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4923056</comments>
            <pubDate>Tue, 31 May 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4923056</guid>        </item>
        <item>
            <title>Increased numbers of circulating ECs are associated with systemic GVHD.</title>
            <link>http://www.medworm.com/index.php?rid=4877129&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21605346%26dopt%3DAbstract</link>
            <description>Conclusion:â€‚ Circulating ECs might be associated with systemic aGVHD.
    PMID: 21605346 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4877129</comments>
            <pubDate>Mon, 23 May 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4877129</guid>        </item>
        <item>
            <title>Factor VIIa-Antithrombin complexes during cardiac surgery using cardiopulmonary bypass.</title>
            <link>http://www.medworm.com/index.php?rid=4877132&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21569219%26dopt%3DAbstract</link>
            <description>Authors: Davidson SJ, Woodhams B
    Antithrombin 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, 20â€ƒmin intervals during cardiopulmonary bypass and postprotamine. The presurgery concentrations of VIIa-antithrombin complexes were median of 52.7pm, a...</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4877132</comments>
            <pubDate>Sun, 15 May 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4877132</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=4877131&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21569220%26dopt%3DAbstract</link>
            <description>Conclusion:â€‚ 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.
    PMID: 21569220 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4877131</comments>
            <pubDate>Sun, 15 May 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4877131</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=4877130&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21569221%26dopt%3DAbstract</link>
            <description>Conclusion:â€‚ 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.
    PMID: 21569221 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4877130</comments>
            <pubDate>Sun, 15 May 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4877130</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=4877133&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21545688%26dopt%3DAbstract</link>
            <description>Conclusion:â€‚ Sampling for pO(2) determination should be carried out in small volumes and assessed within 30â€ƒmin of collection to obtain reliable and comparable results.
    PMID: 21545688 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4877133</comments>
            <pubDate>Thu, 05 May 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4877133</guid>        </item>
        <item>
            <title>Clinical multicenter evaluation of a new FXa-based Antithrombin assay.</title>
            <link>http://www.medworm.com/index.php?rid=4877136&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21535419%26dopt%3DAbstract</link>
            <description>Conclusion:â€‚ The INNOVANCE Antithrombin assay has high sensitivity for Antithrombin deficiencies and is reliable, precise and suitable for routine clinical use.
    PMID: 21535419 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4877136</comments>
            <pubDate>Mon, 02 May 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4877136</guid>        </item>
        <item>
            <title>An evaluation of the Sebia capillarys Neonat Haemoglobin FASTâ„¢ system for routine newborn screening for sickle cell disease.</title>
            <link>http://www.medworm.com/index.php?rid=4877135&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21535479%26dopt%3DAbstract</link>
            <description>Authors: Murray C, Hall SK, Griffiths P
    The West Midlands Newborn Screening Laboratory (NBSL) at Birmingham Children's Hospital (BCH), UK, screens approximately 71â€ƒ000 babies per annum using the Bio-Rad automated VARIANTâ„¢ 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(Â®) isoelectric electric focusing (IEF) kits supplied by Perkin-Elmer. The Sebia capillarys Neonat Haemoglobin FASTâ„¢ system was evaluated as a possible replacement for the first- or second-line methods used. Both the Sebia and Bio-Rad method...</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4877135</comments>
            <pubDate>Mon, 02 May 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4877135</guid>        </item>
        <item>
            <title>Abstracts of the XXIV International Symposium on Technical Innovations in Laboratory Hematology.</title>
            <link>http://www.medworm.com/index.php?rid=4877134&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21535418%26dopt%3DAbstract</link>
            <description>Authors: 
    
    PMID: 21535418 [PubMed - indexed for MEDLINE] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4877134</comments>
            <pubDate>Sat, 30 Apr 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4877134</guid>        </item>
        <item>
            <title>Molecular characterization of glucose-6-phosphate dehydrogenase deficiency in Pakistani population.</title>
            <link>http://www.medworm.com/index.php?rid=4770322&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21507207%26dopt%3DAbstract</link>
            <description>Conclusion:â€‚ 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.
    PMID: 21507207 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4770322</comments>
            <pubDate>Wed, 20 Apr 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4770322</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=4770323&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21501392%26dopt%3DAbstract</link>
            <description>Conclusion:â€‚ 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.
    PMID: 21501392 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4770323</comments>
            <pubDate>Mon, 18 Apr 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4770323</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=4770324&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21492411%26dopt%3DAbstract</link>
            <description>Conclusion:â€‚ 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.
    PMID: 21492411 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4770324</comments>
            <pubDate>Wed, 13 Apr 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4770324</guid>        </item>
        <item>
            <title>The immunophenotypic stability of plasma cell myeloma by flow cytometry.</title>
            <link>http://www.medworm.com/index.php?rid=4770327&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21470371%26dopt%3DAbstract</link>
            <description>Conclusion:â€‚ 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.
    PMID: 21470371 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4770327</comments>
            <pubDate>Wed, 06 Apr 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4770327</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 -Î±(3.7) /-Î±(3.7) in two Brazilian families.</title>
            <link>http://www.medworm.com/index.php?rid=4770326&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21470372%26dopt%3DAbstract</link>
            <description>Conclusion:â€‚ 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.
    PMID: 21470372 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4770326</comments>
            <pubDate>Wed, 06 Apr 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4770326</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=4770325&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21470373%26dopt%3DAbstract</link>
            <description>Conclusion:â€‚ In PCN cases, an FC-assessed 3% PCC in BM aspirates should not be used as a cut-off for further FISH testing.
    PMID: 21470373 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4770325</comments>
            <pubDate>Wed, 06 Apr 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4770325</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=4770328&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21463487%26dopt%3DAbstract</link>
            <description>Conclusion:â€‚ 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.
    PMID: 21463487 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4770328</comments>
            <pubDate>Mon, 04 Apr 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4770328</guid>        </item>
        <item>
            <title>Purging efficacy of ZnPcH(1) -based photodynamic therapy on chronic myeloid leukemia bone marrow.</title>
            <link>http://www.medworm.com/index.php?rid=4770333&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21457188%26dopt%3DAbstract</link>
            <description>Conclusion:â€‚ Our data suggest that ZnPcH(1) -PDT may be a useful modality for purging CML cells for autologous grafts.
    PMID: 21457188 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4770333</comments>
            <pubDate>Sun, 03 Apr 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4770333</guid>        </item>
        <item>
            <title>Limitation of malaria diagnosis with the Cell-Dyn(Â®) analyser: not all haemozoin-containing monocytes are detected or shown.</title>
            <link>http://www.medworm.com/index.php?rid=4770332&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21457189%26dopt%3DAbstract</link>
            <description>Authors: HÃ¤nscheid T, RomÃ£o R, Grobusch MP, Amaral T, Melo-Cristino J
    
    PMID: 21457189 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4770332</comments>
            <pubDate>Sun, 03 Apr 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4770332</guid>        </item>
        <item>
            <title>Screening for CRLF2 overexpression in adult acute lymphoblastic leukemia.</title>
            <link>http://www.medworm.com/index.php?rid=4770331&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21457190%26dopt%3DAbstract</link>
            <description>Authors: Haslam K, Kelly J, Morris T, Connaghan G, Gilligan O, Browne P, Langabeer SE
    
    PMID: 21457190 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4770331</comments>
            <pubDate>Sun, 03 Apr 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4770331</guid>        </item>
        <item>
            <title>Nontransferrin-bound iron in transfused patients with sickle cell disease.</title>
            <link>http://www.medworm.com/index.php?rid=4607236&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21382180%26dopt%3DAbstract</link>
            <description>Authors: Inati A, Musallam KM, Cappellini MD, Duca L, Taher AT
    The value of nontransferrin-bound iron (NTBI) as an index of iron overload in patients with thalassemia has been evaluated; however, data in patients with sickle cell disease (SCD) is limited. NTBI levels were evaluated in a cross-sectional study of 43 transfused patients with SCD. Patient charts were reviewed for demographics, status of the spleen, and total number of lifetime transfusions. All patients were chelation naÃ¯ve and none of the patients had evidence of hepatitis B or C infection. Blood samples were taken for assessment of NTBI and serum ferritin (SF); liver iron concentration (LIC) was determined by R2 magnetic resonance imaging. NTBI levels were generally low with a median of -0.01â€ƒÎ¼m (range -2.56 to 6.37â...</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4607236</comments>
            <pubDate>Fri, 18 Mar 2011 18:15:21 +0100</pubDate>
            <guid isPermaLink="false">4607236</guid>        </item>
        <item>
            <title>The phenotypic and genetic assessment of antithrombin deficiency.</title>
            <link>http://www.medworm.com/index.php?rid=4607235&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21401902%26dopt%3DAbstract</link>
            <description>Conclusion:â€‚ 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.
    PMID: 21401902 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4607235</comments>
            <pubDate>Tue, 15 Mar 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4607235</guid>        </item>
        <item>
            <title>ICSH review of the measurement of the erythocyte sedimentation rate.</title>
            <link>http://www.medworm.com/index.php?rid=4545284&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21352508%26dopt%3DAbstract</link>
            <description>Authors: Jou JM, Lewis SM, Briggs C, Lee SH, DE LA Salle B, McFadden S, 
    In 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 (4â€ƒ:â€ƒ1) or whole blood anticoagulated with sodium citrate (4â€ƒ:â€ƒ1) in Westergren pipettes, (iii) The ESR pipettes can be of glass or plastic (with specific characteristics). It must be colourless; ...</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4545284</comments>
            <pubDate>Fri, 25 Feb 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4545284</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=4545286&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21338473%26dopt%3DAbstract</link>
            <description>Conclusion:â€‚ 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.
    PMID: 21338473 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4545286</comments>
            <pubDate>Tue, 22 Feb 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4545286</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=4545285&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21338474%26dopt%3DAbstract</link>
            <description>Conclusion:â€‚ 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.
    PMID: 21338474 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4545285</comments>
            <pubDate>Tue, 22 Feb 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4545285</guid>        </item>
        <item>
            <title>Megaloblastic pancytopenia vis-Ã -vis non-megaloblastic pancytopenia: is mean platelet volume useful discriminating indicator.</title>
            <link>http://www.medworm.com/index.php?rid=4490115&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21310007%26dopt%3DAbstract</link>
            <description>Conclusion:â€‚ 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.
    PMID: 21310007 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4490115</comments>
            <pubDate>Thu, 10 Feb 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4490115</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=4490114&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21310008%26dopt%3DAbstract</link>
            <description>Conclusion:â€‚ 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.
    PMID: 21310008 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4490114</comments>
            <pubDate>Thu, 10 Feb 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4490114</guid>        </item>
        <item>
            <title>Evaluation of schistocyte monitoring after haematopoietic stem cell transplantation.</title>
            <link>http://www.medworm.com/index.php?rid=4490116&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21284831%26dopt%3DAbstract</link>
            <description>Conclusion:â€‚ 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.
    PMID: 21284831 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4490116</comments>
            <pubDate>Wed, 02 Feb 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4490116</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=4419879&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21272268%26dopt%3DAbstract</link>
            <description>Conclusion:â€‚ 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.
    PMID: 21272268 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4419879</comments>
            <pubDate>Fri, 28 Jan 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4419879</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 Î±-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=4419882&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21266019%26dopt%3DAbstract</link>
            <description>Conclusion:â€‚ A novel StyI restriction enzyme can be used to confirm the commonest type of Hb G-Philadelphia. DNA sequencing identified four other Î±-chain variants with a similar HPLC and IEF phenotype.
    PMID: 21266019 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4419882</comments>
            <pubDate>Wed, 26 Jan 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4419882</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=4419881&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21266020%26dopt%3DAbstract</link>
            <description>Conclusion:â€‚ 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.
    PMID: 21266020 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4419881</comments>
            <pubDate>Wed, 26 Jan 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4419881</guid>        </item>
        <item>
            <title>Performance evaluation of the Celltac F haematology analyser.</title>
            <link>http://www.medworm.com/index.php?rid=4419880&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21266021%26dopt%3DAbstract</link>
            <description>Conclusion:â€‚ 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.
    PMID: 21266021 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4419880</comments>
            <pubDate>Wed, 26 Jan 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4419880</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=4419883&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21251240%26dopt%3DAbstract</link>
            <description>Conclusion:â€‚ 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.
    PMID: 21251240 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4419883</comments>
            <pubDate>Thu, 20 Jan 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4419883</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=4356735&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21219591%26dopt%3DAbstract</link>
            <description>Conclusions:â€‚ 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.
    PMID: 21219591 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4356735</comments>
            <pubDate>Tue, 11 Jan 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4356735</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=4259727&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21143592%26dopt%3DAbstract</link>
            <description>Discussion:â€‚ 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.
    PMID: 21143592 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4259727</comments>
            <pubDate>Thu, 09 Dec 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4259727</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=4228995&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21118380%26dopt%3DAbstract</link>
            <description>Conclusion:â€‚ 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.
    PMID: 21118380 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4228995</comments>
            <pubDate>Wed, 01 Dec 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4228995</guid>        </item>
        <item>
            <title>Heparin-induced thrombocytopenia: evaluation of IgG and IgGAM ELISA assays.</title>
            <link>http://www.medworm.com/index.php?rid=4228994&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21118381%26dopt%3DAbstract</link>
            <description>Conclusion:â€‚ Our data strongly support the use of IgG-only assays for the detection of HIT antibodies.
    PMID: 21118381 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4228994</comments>
            <pubDate>Wed, 01 Dec 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4228994</guid>        </item>
        <item>
            <title>A novel approach for assessments of erythrocyte sedimentation rate.</title>
            <link>http://www.medworm.com/index.php?rid=4228988&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21118382%26dopt%3DAbstract</link>
            <description>Conclusion:â€‚ Thus, unlike Westergren erythrocyte sedimentation rate, sedimentation data obtained by the proposed method do not require correction for Hct.
    PMID: 21118382 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4228988</comments>
            <pubDate>Wed, 01 Dec 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4228988</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=4228970&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21118383%26dopt%3DAbstract</link>
            <description>Authors: Liu YN, Li R, Li J, Li DZ
    
    PMID: 21118383 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4228970</comments>
            <pubDate>Wed, 01 Dec 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4228970</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=4228964&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21118384%26dopt%3DAbstract</link>
            <description>Authors: Zammit G, Farrugia R, Barbara C, Azzopardi L, Inglott AS, Adami MZ, Grech V
    
    PMID: 21118384 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4228964</comments>
            <pubDate>Wed, 01 Dec 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4228964</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=4228963&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21118385%26dopt%3DAbstract</link>
            <description>Conclusion:â€‚ In our study group, a bone marrow biopsy was a useful investigation with a high diagnostic yield.
    PMID: 21118385 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4228963</comments>
            <pubDate>Wed, 01 Dec 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4228963</guid>        </item>
        <item>
            <title>Letter to the Editor.</title>
            <link>http://www.medworm.com/index.php?rid=4228962&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21118386%26dopt%3DAbstract</link>
            <description>Authors: Schindhelm RK, Van Der Zwan LP
    
    PMID: 21118386 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4228962</comments>
            <pubDate>Wed, 01 Dec 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4228962</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=4228961&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21118387%26dopt%3DAbstract</link>
            <description>Conclusion:â€‚ This combination of problems effectively combines to render selective reamplification and redigestion unsuitable for detecting low fractions of the V617F mutation.
    PMID: 21118387 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4228961</comments>
            <pubDate>Wed, 01 Dec 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4228961</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=4228960&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21118388%26dopt%3DAbstract</link>
            <description>Conclusion:â€‚ 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.
    PMID: 21118388 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4228960</comments>
            <pubDate>Wed, 01 Dec 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4228960</guid>        </item>
        <item>
            <title>A case of Plasmodium vivax with unusual enlarged gametocytes.</title>
            <link>http://www.medworm.com/index.php?rid=4159420&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21054814%26dopt%3DAbstract</link>
            <description>Authors: Hahm C, Huh J, Hwang YS, Choi HJ, Yang HJ, Chung WS
    
    PMID: 21054814 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4159420</comments>
            <pubDate>Thu, 04 Nov 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4159420</guid>        </item>
        <item>
            <title>Nonsense mutation of Î²-globin gene at codon 82 (AAGâ†’TAG) or HBB:C247 Aâ†’T with polymorphism: cause of thalassemia intermedia?</title>
            <link>http://www.medworm.com/index.php?rid=4159419&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21054815%26dopt%3DAbstract</link>
            <description>Authors: Kumar R, Agarwal S
    
    PMID: 21054815 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4159419</comments>
            <pubDate>Thu, 04 Nov 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4159419</guid>        </item>
        <item>
            <title>Resistance to aspirin and clopidogrel therapy.</title>
            <link>http://www.medworm.com/index.php?rid=4159425&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21054811%26dopt%3DAbstract</link>
            <description>Conclusion:â€‚ Data from ongoing and future studies are awaited to better understand this entity and to highlight the most appropriate treatment strategies.
    PMID: 21054811 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4159425</comments>
            <pubDate>Wed, 03 Nov 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4159425</guid>        </item>
        <item>
            <title>Cryoglobulin detection from blood and peritoneal fluid smears.</title>
            <link>http://www.medworm.com/index.php?rid=4159422&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21054812%26dopt%3DAbstract</link>
            <description>Authors: Lesesve JF, Muller M, Vautrin A, Odinotte A, Etienne Y
    Laboratory identification of cytoplasmic inclusions in leucocytes as unusual manifestation of cryoglobulinemia has been previously reported (Maitra etÂ al., 2000 American Journal of Clinical Pathology, 113, 107-112; Fohlen-Walter etÂ 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.
    PMID: 21054812 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4159422</comments>
            <pubDate>Wed, 03 Nov 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4159422</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=4159421&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21054813%26dopt%3DAbstract</link>
            <description>Conclusion:â€‚ 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.
    PMID: 21054813 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4159421</comments>
            <pubDate>Wed, 03 Nov 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4159421</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=4111140&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20979595%26dopt%3DAbstract</link>
            <description>Conclusion:â€‚ The data showed a statistically significant difference between glass and plastic tubes in the normal population only for the PT test, with consequent repercussions for patients on OAT. This means that appropriate care and validation should take place whenever there is a change in tube type.
    PMID: 20979595 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4111140</comments>
            <pubDate>Tue, 26 Oct 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4111140</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=4082582&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20942870%26dopt%3DAbstract</link>
            <description>Conclusions:â€‚ Thus, the MFI ratio B-CLL/T cell corrected by isotype is a reliable analysis technique to estimate ZAP-70 expression in B-CLL.
    PMID: 20942870 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4082582</comments>
            <pubDate>Wed, 06 Oct 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4082582</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=4082583&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20942869%26dopt%3DAbstract</link>
            <description>Conclusion:â€‚ K562r due to duplication of autophosphorylation of wild-type Bcr-Abl induced by imatinib was still partially resistant to dasatinib and nilotinib, but this was overcome by incremental dosing. Rapamycin did not enhance imatinib sensitivity. The blockade of the ubiquitin-proteasome pathway could be effective in overcoming resistance in the K562r imatinib-resistant cell line.
    PMID: 20942869 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4082583</comments>
            <pubDate>Sun, 03 Oct 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4082583</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=4031613&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20880301%26dopt%3DAbstract</link>
            <description>Conclusion:â€‚ This review has demonstrated that no significant coagulation factor deficiency would be left undiagnosed if the protocol was followed. This would have considerably reduced the cost and time spent performing these assays.
    PMID: 20880301 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4031613</comments>
            <pubDate>Tue, 28 Sep 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4031613</guid>        </item>
        <item>
            <title>Serum hepcidin-25 may replace the ferritin index in the Thomas plot in assessing iron status in anemic patients.</title>
            <link>http://www.medworm.com/index.php?rid=4017935&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20868446%26dopt%3DAbstract</link>
            <description>Conclusion:Ã¢Â€Â‚ Patients with IDA can be differentiated from ACD and ACD/IDA but not ACD from ACD/IDA based on hepcidin-25 alone. The combination of hepcidin-25 with CHr in the hepcidin-25 plot was useful for the differentiation of the states above.
    PMID: 20868446 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4017935</comments>
            <pubDate>Sun, 26 Sep 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4017935</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=4017934&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20868447%26dopt%3DAbstract</link>
            <description>Conclusion:Ã¢Â€Â‚ Since population genetic studies on VNTR loci are not well established in Southeast Asia, the present study is useful to determine reliable markers during the initial screening step of chimerism analysis. By following this algorithm, we are able to reduce time and cost of finding a suitable VNTR marker in our cohort.
    PMID: 20868447 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4017934</comments>
            <pubDate>Sun, 26 Sep 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4017934</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=4017936&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20860735%26dopt%3DAbstract</link>
            <description>Conclusion:Ã¢Â€Â‚ Calculating a ratio between the LA-sensitive PTT-LA and the less sensitive Pathromtin-SL improves the performance of the PTT-LA itself and represents a simple and sensitive aPTT-based integrated strategy for LA screening.
    PMID: 20860735 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4017936</comments>
            <pubDate>Wed, 22 Sep 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4017936</guid>        </item>
        <item>
            <title>The responsiveness of different APTT reagents to mild factor VIII, IX and XI deficiencies.</title>
            <link>http://www.medworm.com/index.php?rid=3977130&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20840376%26dopt%3DAbstract</link>
            <description>Conclusion:Ã¢Â€Â‚ Both Synthasil and Actin FS are acceptable reagents to screen for reduced factors VIII, IX and XI, and the number of mildly reduced factors not diagnosed will be limited.
    PMID: 20840376 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3977130</comments>
            <pubDate>Mon, 13 Sep 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3977130</guid>        </item>
        <item>
            <title>Comparison of the BioRad Variant and Primus Ultra2 high-pressure liquid chromatography (HPLC) instruments for the detection of variant hemoglobins.</title>
            <link>http://www.medworm.com/index.php?rid=3977129&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20840377%26dopt%3DAbstract</link>
            <description>Conclusion:Ã¢Â€Â‚ Both Variant and Ultra2 HPLC methods were able to detect most common hemoglobin variants. There was better discrimination for fast hemoglobins, between hemoglobins E and A(2) , and between hemoglobins S and F using the Ultra2 HPLC method.
    PMID: 20840377 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3977129</comments>
            <pubDate>Mon, 13 Sep 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3977129</guid>        </item>
        <item>
            <title>Evaluation of three commercial ELISA kits for anticardiolipin and anti-beta2-glycoprotein I antibodies in the laboratory diagnosis of the antiphospholipid syndrome.</title>
            <link>http://www.medworm.com/index.php?rid=3943791&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20813022%26dopt%3DAbstract</link>
            <description>Conclusion: All evaluated ELISAs are a practical tool in the laboratory diagnosis of APS. The diagnostic performance shows slight differences between the ELISAs from the different manufacturers.
    PMID: 20813022 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3943791</comments>
            <pubDate>Mon, 30 Aug 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3943791</guid>        </item>
        <item>
            <title>Stability of CoaguChek XS test strip is not effected by frequency of air exposure.</title>
            <link>http://www.medworm.com/index.php?rid=3904000&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20731731%26dopt%3DAbstract</link>
            <description>Authors: Son KH, Ahn CB, An H, Choe G, Lee SH, Sun K
    
    PMID: 20731731 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3904000</comments>
            <pubDate>Sat, 21 Aug 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3904000</guid>        </item>
        <item>
            <title>Stability and robustness of blood variables in an antidoping context.</title>
            <link>http://www.medworm.com/index.php?rid=3887248&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20718874%26dopt%3DAbstract</link>
            <description>Conclusion: In conclusion, our data clearly demonstrate that as long as the World Anti-Doping Agency's guidelines are followed rigorously, all blood results reach the quality level required in the antidoping context.
    PMID: 20718874 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3887248</comments>
            <pubDate>Sun, 15 Aug 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3887248</guid>        </item>
        <item>
            <title>The new haematology analyzer DxH 800: an evaluation of the analytical performances and leucocyte flags, comparison with the LH 755.</title>
            <link>http://www.medworm.com/index.php?rid=3887247&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20718875%26dopt%3DAbstract</link>
            <description>Conclusion: The DxH 800 provides reliable results and increases laboratory efficiency by reducing working time and costs associated with the optical validation of the results.
    PMID: 20718875 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3887247</comments>
            <pubDate>Sun, 15 Aug 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3887247</guid>        </item>
        <item>
            <title>Increasing hematopoietic microchimerism is a reliable indicator of incipient AML relapse.</title>
            <link>http://www.medworm.com/index.php?rid=3828210&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20681999%26dopt%3DAbstract</link>
            <description>Conclusion: Within this paper, we emphasize the importance of microchimerism monitoring as a reliable indicator of incipient AML relapse, especially in patients where no other specific molecular marker is available.
    PMID: 20681999 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3828210</comments>
            <pubDate>Sun, 01 Aug 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3828210</guid>        </item>
        <item>
            <title>Hematopoietic stem cell lodgment in the adult bone marrow stem cell niche.</title>
            <link>http://www.medworm.com/index.php?rid=3828209&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20682000%26dopt%3DAbstract</link>
            <description>Authors: Lam BS, Adams GB
    Summary Treatment of malignant blood disorders, such as leukemia, that can provide a better chance of long-term remission involves myeloablation followed by transplantation of matched donor hematopoietic stem cells (HSCs). For successful engraftment and re-establishment of hematopoiesis to occur in the recipient, the transplanted HSCs must first migrate from the blood circulation to the bone marrow (BM), a process known as homing, then localize and anchor in suitable microenvironments within the BM, a process known as lodgment. After lodgment, the specific fate of the transplanted HSCs is determined through complex, bidirectional interactions with various stromal cell components in the niche. Ultimately, these interactions dictate the clinical outcome of the t...</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3828209</comments>
            <pubDate>Sun, 01 Aug 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3828209</guid>        </item>
        <item>
            <title>CD95 is not functional in human erythrocytes.</title>
            <link>http://www.medworm.com/index.php?rid=3828208&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20682001%26dopt%3DAbstract</link>
            <description>Conclusion: Based on some key features for an activated CD95 system, this death receptor has been considered to induce PS exposure. However, we give evidence, that CD95 is not functional in red blood cells and that activation of this death receptor does not lead to the exposure of phosphatidylserine.
    PMID: 20682001 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3828208</comments>
            <pubDate>Sun, 01 Aug 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3828208</guid>        </item>
        <item>
            <title>Occurrence of common and rare delta-globin gene defects in two multiethnic populations: thirteen new mutations and the significance of delta-globin gene defects in beta-thalassemia diagnostics.</title>
            <link>http://www.medworm.com/index.php?rid=3828212&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20678137%26dopt%3DAbstract</link>
            <description>Conclusion: HbA2 mutations either structurally stable and visible or undetectable because of a thalassemia effect or instability are clinically asymptomatic but may compromise the diagnosis of beta-thalassemia minor. Stable mutations result in two HbA2 fractions of about half of the expected value. Expression defects are undetectable as a protein fraction but reduce the amount of HbA2 by half.
    PMID: 20678137 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3828212</comments>
            <pubDate>Wed, 28 Jul 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3828212</guid>        </item>
        <item>
            <title>Routine diagnostic procedures of myelodysplastic syndromes: value of a structural blood cell parameter (NEUT-X) determined by the Sysmex XE-2100.</title>
            <link>http://www.medworm.com/index.php?rid=3813987&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20670338%26dopt%3DAbstract</link>
            <description>Conclusion: Including the GI index in the routine parameters provided by the Sysmex analyzer could be of major help for nonspecialized routine laboratories in detecting MDS.
    PMID: 20670338 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3813987</comments>
            <pubDate>Wed, 28 Jul 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3813987</guid>        </item>
        <item>
            <title>CD66c expression in B-cell acute lymphoblastic leukemia: strength and weakness.</title>
            <link>http://www.medworm.com/index.php?rid=3813989&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20666852%26dopt%3DAbstract</link>
            <description>Conclusion: CD66c expression is correlated, but not specifically, with BCR/ABL1 rearrangement. It would seem better to interpret the absence of CD66c expression with a lack of BCR/ABL1 rearrangement. This myeloid antigen could be interesting in the detection of minimal residual disease.
    PMID: 20666852 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3813989</comments>
            <pubDate>Tue, 27 Jul 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3813989</guid>        </item>
        <item>
            <title>Diagnosing myelodysplastic/myeloproliferative neoplasms: laboratory testing strategies to exclude other disorders.</title>
            <link>http://www.medworm.com/index.php?rid=3813988&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20670271%26dopt%3DAbstract</link>
            <description>Conclusion: The most appropriate classification of myeloid neoplasms presenting with hybrid myelodysplastic/myeloproliferative features requires a comprehensive clinical and laboratory assessment with careful integration of the morphological, immunophenotypic, genetic, and clinical characteristics.
    PMID: 20670271 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3813988</comments>
            <pubDate>Tue, 27 Jul 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3813988</guid>        </item>
        <item>
            <title>Compound heterozygosity for a rare small deletion and a common point mutation in the beta-globin gene: report of two Chinese families.</title>
            <link>http://www.medworm.com/index.php?rid=3787427&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20649908%26dopt%3DAbstract</link>
            <description>Conclusion: Patient B is the second report of the CD54-58(-13 bp) deletion. However, our report differs from the previous report in two ways: we performed a family study based on multiple samples; and the carriers and patient showed an elevated level of HbF, which was not observed in the previous case.
    PMID: 20649908 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3787427</comments>
            <pubDate>Thu, 22 Jul 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3787427</guid>        </item>
        <item>
            <title>A study of atypical APTT derivative curves on the ACL TOP coagulation analyser.</title>
            <link>http://www.medworm.com/index.php?rid=3787426&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20649909%26dopt%3DAbstract</link>
            <description>Conclusion: Atypical derivative curves seen in ellagic acid APTTs are of limited diagnostic use because of the frequency with which they occur. This may be related to the need to optimize the data reduction utilized on the ACL TOP for these reagents. With silica activator APTTs, the presence of atypical derivative curves proved to be a very simple tool when troubleshooting unexpected abnormal APTT results, commonly predicting a factor deficiency or LA that would warrant further investigation. The cause of these aberrant derivative curves is probably related to abnormal thrombin generation in the APTT test and warrants further study.
    PMID: 20649909 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3787426</comments>
            <pubDate>Thu, 22 Jul 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3787426</guid>        </item>
        <item>
            <title>Hemoglobin F levels influence the results of NESTROFT: replication in two surveys.</title>
            <link>http://www.medworm.com/index.php?rid=3762577&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20633055%26dopt%3DAbstract</link>
            <description>Authors: Mamtani M, Chatterjee N, Mishra A, Soni R, Jawahirani A, Das K, Rughwani V, Shrivastava M, Kulkarni H
    
    PMID: 20633055 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3762577</comments>
            <pubDate>Mon, 12 Jul 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3762577</guid>        </item>
        <item>
            <title>Recent advances in the diagnosis and classification of myeloid neoplasms - comments on the 2008 WHO classification.</title>
            <link>http://www.medworm.com/index.php?rid=3762578&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20626469%26dopt%3DAbstract</link>
            <description>Authors: Yin CC, Medeiros LJ, Bueso-Ramos CE
    Summary The fourth edition of the World Health Organization (WHO) classification of myeloid neoplasms refined the criteria for some previously described myeloid neoplasms and recognized several new entities based on recent elucidation of molecular pathogenesis, identification of new diagnostic and prognostic markers, and progress in clinical management. Protein tyrosine kinase abnormalities, including translocations or mutations involving ABL1, JAK2, MPL, KIT, PDGFRA, PDGFRB, and FGFR1, have been used as the basis for classifying myeloproliferative neoplasms (MPN). Two new entities - refractory cytopenia with unilineage dysplasia and refractory cytopenia of childhood have been added to the group of myelodysplastic syndromes (MDS), and 'refra...</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3762578</comments>
            <pubDate>Tue, 06 Jul 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3762578</guid>        </item>
        <item>
            <title>Interlaboratory variability of CD34+ stem cell enumeration. A pilot study to national external quality assessment within the Czech Republic.</title>
            <link>http://www.medworm.com/index.php?rid=3684570&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20561093%26dopt%3DAbstract</link>
            <description>This study was successful in reducing the interinstitutional variability of CD34+ enumeration. It was shown that the implementation of a standardized protocol does not guarantee accurate measurement. Our research design represents a useful tool, which allows verification of the proper use of a standardized method, the training of operators and feedback in response to the survey results.
    PMID: 20561093 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3684570</comments>
            <pubDate>Tue, 15 Jun 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3684570</guid>        </item>
        <item>
            <title>The incidence of malaria and the comparison of hematological and biochemical indices of Plasmodium falciparum-parasitemic and aparasitemic sickle cell disease (SCD) patients.</title>
            <link>http://www.medworm.com/index.php?rid=3604078&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20497486%26dopt%3DAbstract</link>
            <description>Authors: Nsiah K, Dzogbefia VP, Ansong D, Boateng H, Ocloo D, Osei-Frempong E, Kena Frempong N, Osei Akoto A
    Summary Hemolytic anemia is common in sickle cell disease (SCD), but the course and extent differ, depending on genetic, epigenetic, and environmental factors. In the malaria-endemic tropical environment, some vulnerable subjects would be infected and the impact of infection would vary. Therefore, this study was to find malaria incidence and the associated changes in some laboratory indices in 330 SCD subjects. Following blood smear preparation for falciparum detection, hematological and biochemical indices were measured for a comparison of parasitemic and age-matched, genotype-matched, and sex-matched nonparasitemics. For sixty-nine parasitemics, constituting about 21% of all s...</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3604078</comments>
            <pubDate>Sat, 22 May 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3604078</guid>        </item>
        <item>
            <title>The role of automated measurement of red cell subpopulations on the Sysmex XE 5000 analyzer in the differential diagnosis of microcytic anemia.</title>
            <link>http://www.medworm.com/index.php?rid=3604080&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20492000%26dopt%3DAbstract</link>
            <description>Authors: Urrechaga E, Borque L, Escanero JF
    Summary Cell counter-based formulae have been used in the differential diagnosis of microcytic anemia. The measurement of new red cell parameters is now available on the Sysmex XE 5000 analyzer. Derived from the percentages of microcytic and hypochromic red cells, the authors describe the new formula %microcytic-%hypochromic, M-H index. The aim of this study was to assess the discriminant value of this new index in the differential diagnosis of microcytic anemia and thalassemia screening compared to the published indices. Receiver operating characteristic curves, sensitivity, specificity and Youden index were calculated for a set of 170 iron-deficiency anemia patients and 200 beta thalassemia carriers. % microcytic-% hypochromic index showed ...</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3604080</comments>
            <pubDate>Mon, 17 May 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3604080</guid>        </item>
        <item>
            <title>Serum prohepcidin positively correlates with erythropoietin in normal adults.</title>
            <link>http://www.medworm.com/index.php?rid=3604079&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20492001%26dopt%3DAbstract</link>
            <description>Authors: Li XY, Li JH, Jiang Y, Peng BS, Li J, Zhu SL, Su ZW, Chang JP
    
    PMID: 20492001 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3604079</comments>
            <pubDate>Mon, 17 May 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3604079</guid>        </item>
        <item>
            <title>Expression of bone morphogenetic proteins (BMPs) receptors in patients with B-cell chronic lymphocytic leukemia (B-CLL).</title>
            <link>http://www.medworm.com/index.php?rid=3604085&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20491995%26dopt%3DAbstract</link>
            <description>Authors: Dzietczenia J, WrÃƒÂ³bel T, JaÃ…Âºwiec B, Mazur G, Butrym A, PorÃ„Â™ba R, Kuliczkowski K
    Summary Bone morphogenetic proteins (BMPs) are multifunctional cytokines which belong to transforming growth factor beta (TGF beta) superfamily. They regulate proliferation, differentiation, and apoptosis in a variety of cells including hematopoietic cells. BMPs act because of binding to two types of serine/threonine kinase receptors: BMP type I receptors (IA and IB) and BMP type II receptor. Deregulation of BMPs signaling pathways has been reported in some of human cancers, but the role of BMPs in hematopoietic malignancies remains unknown. The aim of our study was to examine the percentage of expression of BMPs receptors on lymphocytes of patients with B-cell chronic lymphocytic leukemia...</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3604085</comments>
            <pubDate>Sun, 09 May 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3604085</guid>        </item>
        <item>
            <title>Initial performance evaluation of the UniCel((R)) DxH 800 Coulter((R)) cellular analysis system.</title>
            <link>http://www.medworm.com/index.php?rid=3604084&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20491996%26dopt%3DAbstract</link>
            <description>Authors: Hedley BD, Keeney M, Chin-Yee I, Brown W
    Summary The Beckman Coulter UniCel((R)) DxH 800 is a hematology analyzer incorporating new electronic and mechanical design with advanced algorithm technology to perform CBC, white blood cell (WBC) differential, nucleated red blood cell (NRBC), and reticulocyte analysis. Evaluation of this instrument was performed in our 800-bed tertiary care hospital and specifically centered upon the correlation of WBC, NRBC, and platelet (PLT) enumeration when compared to a predicate analyzer, the Coulter((R)) LH 780, and flow cytometry (FCM) reference methods. Of particular interest were those samples with morphologically confirmed interference and extreme leukocytosis (evaluated with respect to red blood cell parameter correction). The sample set (...</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3604084</comments>
            <pubDate>Sun, 09 May 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3604084</guid>        </item>
        <item>
            <title>Sensitive detection and quantification of minimal residual disease in chronic myeloid leukaemia using nested quantitative PCR for BCR-ABL DNA.</title>
            <link>http://www.medworm.com/index.php?rid=3604083&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20491997%26dopt%3DAbstract</link>
            <description>Authors: Bartley PA, Ross DM, Latham S, Martin-Harris MH, Budgen B, Wilczek V, Branford S, Hughes TP, Morley AA
    Summary Increasing numbers of patients with chronic myeloid leukaemia (CML) treated with tyrosine kinase inhibitors achieve undetectable levels of BCR-ABL mRNA using sensitive quantitative real-time reverse transcriptase PCR (RT-qPCR) methods and a method to measure minimal residual disease (MRD) in patients with low levels could be of value. Following isolation and sequencing of the patient-specific BCR-ABL breakpoint, a DNA-based nested qPCR assay was established, and MRD was measured by this method and one-round RT-qPCR in 38 samples from 24 patients with CML. Mixing experiments using patient DNA in normal DNA indicated that DNA qPCR could detect BCR-ABL sequences at a lim...</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3604083</comments>
            <pubDate>Sun, 09 May 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3604083</guid>        </item>
        <item>
            <title>Analysis of reticulocyte parameters on the Sysmex XE 5000 and LH 750 analyzers in the diagnosis of inefficient erythropoiesis.</title>
            <link>http://www.medworm.com/index.php?rid=3604082&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20491998%26dopt%3DAbstract</link>
            <description>Authors: Urrechaga E, Borque L, Escanero JF
    Summary The reticulocyte hemoglobin equivalent (Ret He) represents an indirect measure of the functional iron available for erythropoiesis over the previous 2-3 days. Only the analyzers of a single manufacturer, Sysmex (Sysmex Corporation, Kobe, Japan), include Ret He. Red blood cell size factor (RSf) is a new parameter provided by Beckman Coulter, which joins together the volume of the erythrocytes and the volume of reticulocytes. The aims of the study were to investigate the clinical usefulness of RSf in the study of erythropoiesis status and to assess its concordance with Ret He values. Samples from 417 patients were run on both LH 780 (Beckman Coulter) and Sysmex XE 5000 analyzers. Independent samples t-test, Pearson correlation, receiver...</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3604082</comments>
            <pubDate>Sun, 09 May 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3604082</guid>        </item>
        <item>
            <title>British Society of Haematology, Slide Session presented at the Annual Scientific Meeting, Brighton 2009.</title>
            <link>http://www.medworm.com/index.php?rid=3604081&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20491999%26dopt%3DAbstract</link>
            <description>Authors: McLornan DP, Burthem J, Duncombe A, Hatton C, Hutchinson CV, Marsden K, Macartney CM, Smith-Straney T, Uprichard J, Wallis J, Webb S, Wilkins BS, McMullin MF
    Summary Seven cases were discussed by an expert panel at the 2009 Annual Scientific Meeting of the British Society of Haematology. These cases are presented in a similar format to that adopted for the meeting. There was an initial discussion of the presenting morphology, generation of differential diagnoses and then, following display of further presenting and diagnostic information, each case was concluded with provision of a final diagnosis.
    PMID: 20491999 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3604081</comments>
            <pubDate>Sun, 09 May 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3604081</guid>        </item>
        <item>
            <title>An allelic typing method for 2DS4 variant used in study of haplotypes of killer cell immunoglobulin-like receptor gene.</title>
            <link>http://www.medworm.com/index.php?rid=3557591&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20456519%26dopt%3DAbstract</link>
            <description>Authors: Bao X, Hou L, Sun A, Chen M, Chen Z, He J
    Summary The KIR2DS4 variants differ in exon 5 and play a role in hematopoietic stem cells transplantation (HSCT). A sequence-based testing (SBT) and TOPO TA cloning system identifying and distinguishing alleles of the KIR2DS4 gene was established and applied to a total of 150 Chinese-Han individuals: 75 patients received T-cell-depleted HSCT and their unrelated donors. The majority (139) of the 150 samples (92.7%) were positive for KIR2DS4. Four of the nine known KIR2DS4 alleles, KIR2DS4 *00101, *003,*004, and *007, were identified. In the haplotype A/A group, a higher risk of acute graft-versus-host disease (aGVHD) was seen when the donor carried two full-length KIR2DS4 alleles (RR 9.0 [95% CI 1.2-66.9], P = 0.010). Our findings sugge...</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3557591</comments>
            <pubDate>Thu, 22 Apr 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3557591</guid>        </item>
        <item>
            <title>The immature platelet fraction is a useful marker for predicting the timing of platelet recovery in patients with cancer after chemotherapy and hematopoietic stem cell transplantation.</title>
            <link>http://www.medworm.com/index.php?rid=3557584&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20456520%26dopt%3DAbstract</link>
            <description>Authors: Yamaoka G, Kubota Y, Nomura T, Inage T, Arai T, Kitanaka A, Saigo K, Iseki K, Baba N, Taminato T
    Summary Prediction of the timing of platelet recovery after chemotherapy and hematopoietic stem cell transplantation (HSCT) allows for optimal platelet transfusion. We assessed the clinical utility of the percentage value of the immature platelet fraction (IPF%) monitored using an XE-2100 automated hematology analyzer to predict the timing of platelet recovery after chemotherapy and HSCT. The IPF% was serially monitored in 31 patients with cancer who received 66 courses of chemotherapy and HSCT. In patients with cancer undergoing chemotherapy and HSCT, a transient increase in IPF% was observed 1-11 days prior to platelet recovery (&amp;gt;30 x 10(9)/l). In patients undergoing chemother...</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3557584</comments>
            <pubDate>Thu, 22 Apr 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3557584</guid>        </item>
        <item>
            <title>Rationale for using insensitive quality control rules for today's hematology analyzers.</title>
            <link>http://www.medworm.com/index.php?rid=3494745&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20402824%26dopt%3DAbstract</link>
            <description>Authors: Cembrowski GS, Smith B, Tung D
    Summary Diverse approaches have been used to assure the analytical quality of automated hematology; as such, there is great variation in their error detection capabilities. We summarize the intralaboratory performance of a cohort of Sysmex XE-2100's running e-Check hematology quality control (QC). The imprecisions of a median performing (50th percentile imprecision) and more imprecise [15th percentile (15P) imprecision] Sysmex XE-2100 are compared with measures of total allowable error (regulatory and physiologically based) to obtain multiples of the usual imprecision that must be detected to prevent the hematology analyzer from producing medically unacceptable results. The resultant large multiples of the usual imprecision (s) demonstrate the ne...</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3494745</comments>
            <pubDate>Thu, 15 Apr 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3494745</guid>        </item>
        <item>
            <title>Performance evaluation of the Abbott CELL-DYN Ruby and the Sysmex XT-2000i haematology analysers.</title>
            <link>http://www.medworm.com/index.php?rid=3494746&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20402823%26dopt%3DAbstract</link>
            <description>Authors: Leers MP, Goertz H, Feller A, Hoffmann JJ
    Summary Two mid-range haematology analysers (Abbott CELL-DYN Ruby and Sysmex XT-2000i) were evaluated to determine their analytical performance and workflow efficiency in the haematology laboratory. In total 418 samples were processed for determining equivalence of complete blood count (CBC) measurements, and 100 for reticulocyte comparison. Blood smears served for assessing the agreement of the differential counts. Inter-instrument agreement for most parameters was good although small numbers of discrepancies were observed. Systematic biases were found for mean cell volume, reticulocytes, platelets and mean platelet volume. CELL-DYN Ruby WBC differentials were obtained with all samples while the XT-2000i suppressed differentials parti...</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3494746</comments>
            <pubDate>Mon, 05 Apr 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3494746</guid>        </item>
        <item>
            <title>Comparison of JAK2 V617F burden quantitation by two different quantitative-polymerase chain reaction methods.</title>
            <link>http://www.medworm.com/index.php?rid=3404314&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20331762%26dopt%3DAbstract</link>
            <description>Authors: Le Bars H, Boulland ML, Bareau B, Grosbois B, Corolleur M, Lamy T, Fardel O
    
    PMID: 20331762 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3404314</comments>
            <pubDate>Tue, 23 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3404314</guid>        </item>
        <item>
            <title>The analysis of JAK2 and MPL mutations and JAK2 single nucleotide polymorphisms in MPN patients by MassARRAY assay.</title>
            <link>http://www.medworm.com/index.php?rid=3404313&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20331763%26dopt%3DAbstract</link>
            <description>Authors: Zhang SJ, Qiu HX, Li JY, Shi JY, Xu W
    Summary Recent studies have shown that JAK2 V617F, MPL W515L/K and JAK2 exon 12 mutations underlie the major molecular pathogenesis of myeloproliferative disorders (MPN). Allele-Specific Polymerase Chain Reaction (AS-PCR), direct sequencing and MassARRAY assay were used to ascertain the real prevalence of these mutations and the influence of genetic susceptibility in Chinese MPN patients. The positive rate of JAK2 V617F in polycythaemia vera (PV), essential thrombocythaemia (ET) and primary myelofibrosis (PMF) was 82.0%, 36.6% and 51.1% respectively. One ET patient and two PMF patients harboured the MPL W515L mutation and three PV patients harboured JAK2 exon 12 mutations. All of these patients were confirmed as JAK2 V617F negative. Clinic...</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3404313</comments>
            <pubDate>Tue, 23 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3404313</guid>        </item>
        <item>
            <title>Performance evaluation of the body fluid mode on the platform Sysmex XE-5000 series automated hematology analyzer.</title>
            <link>http://www.medworm.com/index.php?rid=3383581&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20236183%26dopt%3DAbstract</link>
            <description>Authors: Paris A, Nhan T, Cornet E, Perol JP, Malet M, Troussard X
    Summary We evaluated the performance of the automated body fluid mode of the Sysmex XE-5000 series automated haematology analyzer and compared the performance of the automated method for obtaining white blood cell (WBC), red blood cell (RBC) counts and WBC differential counts with microscopic method. One hundred and seventy-four samples were analysed: 81 ascitic fluid, 32 cerebrospinal fluid (CSF), 26 pleural fluid (PF), 18 synovial fluid (SF), 13 peritoneal fluid (PeF) and 4 other types. The agreement between the automated method and the manual reference showed high correlation, with Pearson correlation coefficients greater than 0.9 for all types of body fluids. We also demonstrate that the automated body fluid analysi...</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3383581</comments>
            <pubDate>Wed, 03 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3383581</guid>        </item>
        <item>
            <title>Race-specific WBC and neutrophil count reference intervals.</title>
            <link>http://www.medworm.com/index.php?rid=3383580&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20236184%26dopt%3DAbstract</link>
            <description>The objective is to establish race-specific reference intervals for WBC and ANC using US National Health and Nutrition Examination Survey (NHANES) of 2000-2003. A total of 14 184 civilian noninstitutionalized US citizens participated in NHANES 2000-2003 had complete blood count, red cell distribution width, platelet count and automated WBC differential determined on a Coulter MAXM. The exclusion criteria were used: ferritin &amp;lt;12 ng/ml, pregnancy, body mass index &amp;gt;30, diastolic blood pressure &amp;gt;100 mm Hg, creatinine &amp;gt;2.5 mg/dl, glucose &amp;gt;126 mg/dl. Data were separated into six sex/race categories: female non-Hispanic white, non-Hispanic black (NHBF)], Mexican American; male non-Hispanic white, non-Hispanic black (NHBM), Mexican American and two age groupings (12-18 and &amp;gt;18 ye...</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3383580</comments>
            <pubDate>Wed, 03 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3383580</guid>        </item>
        <item>
            <title>Association between the neutrophil myeloperoxidase index and subsets of bacterial infections.</title>
            <link>http://www.medworm.com/index.php?rid=3343070&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20201994%26dopt%3DAbstract</link>
            <description>Conclusion] These results indicate that MPXI is correlated with some specific infectious states, i.e. MPXI is low in bacterial sepsis and high in nontuberculous nonseptic bacterial infections. MPXI appears to be an independent and useful biomarker for the diagnosis and follow-up of infectious diseases, especially when the MPXI values are obtained at regular intervals during the disease courses of the patients.
    PMID: 20201994 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3343070</comments>
            <pubDate>Thu, 25 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3343070</guid>        </item>
        <item>
            <title>Characteristic distribution of iron in the bone marrow after parenteral iron therapy.</title>
            <link>http://www.medworm.com/index.php?rid=3343069&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20201995%26dopt%3DAbstract</link>
            <description>Authors: Islam MS, Anoop P
    
    PMID: 20201995 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3343069</comments>
            <pubDate>Thu, 25 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3343069</guid>        </item>
        <item>
            <title>Prognostic value of serum CA125 levels in diffuse large B-cell lymphoma: potential role of a new sex- and age-adjusted reference value.</title>
            <link>http://www.medworm.com/index.php?rid=3343068&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20201996%26dopt%3DAbstract</link>
            <description>Authors: Guti&amp;#xE9;rrez A, Mart&amp;#xED;nez-Serra J, Barcel&amp;#xF3; B, Sampol A, Vi&amp;#xF1;as L, Gonz&amp;#xE1;lez G, Bea MD, Amat JC, Mart&amp;#xED;n J, Ramos R, Bautista A, Forteza-Rey J, Rodr&amp;#xED;guez J, Besalduch J
    Summary CA125, a tumor marker normally used to follow the clinical course of ovarian cancer, also may have a role in lymphoma. All available series were analyzed using the standard reference value 35 U/ml, but age and sex may influence serum CA125 (sCA125) levels. We aim to study the prognostic value of serum CA125 (sCA125) levels in diffuse large B-cell lymphoma (DLBCL), considering the influence of age and sex on sCA125 levels. We investigated the relationship between sCA125 and clinical outcome after treatment in 42 patients with DLBCL, comparing both the standard (35 U/ml) and a n...</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3343068</comments>
            <pubDate>Thu, 25 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3343068</guid>        </item>
        <item>
            <title>Nontransferrin-bound iron in transfused patients with sickle cell disease.</title>
            <link>http://www.medworm.com/index.php?rid=3343067&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20201997%26dopt%3DAbstract</link>
            <description>Authors: Inati A, Musallam KM, Cappellini MD, Duca L, Taher AT
    Summary The value of nontransferrin-bound iron (NTBI) as an index of iron overload in patients with thalassemia has been evaluated; however, data in patients with sickle cell disease (SCD) is limited. NTBI levels were evaluated in a cross-sectional study of 43 transfused patients with SCD. Patient charts were reviewed for demographics, status of the spleen, and total number of lifetime transfusions. All patients were chelation na&amp;#xEF;ve and none of the patients had evidence of hepatitis B or C infection. Blood samples were taken for assessment of NTBI and serum ferritin (SF); liver iron concentration (LIC) was determined by R2 magnetic resonance imaging. NTBI levels were generally low with a median of -0.01 mum (range -2.5...</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3343067</comments>
            <pubDate>Thu, 25 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3343067</guid>        </item>
        <item>
            <title>Characterisation and relevance of CD138-negative plasma cells in plasma cell myeloma.</title>
            <link>http://www.medworm.com/index.php?rid=3343066&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20201998%26dopt%3DAbstract</link>
            <description>Conclusion: We have characterised the CD138(-) PCs as more immature and with a significantly higher proliferative potential. The current trend to ignore this more immature and proliferative subpopulation of malignant PCs may have serious implications when determining gene expression, classifications and drug sensitivity of the malignancy.
    PMID: 20201998 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3343066</comments>
            <pubDate>Thu, 25 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3343066</guid>        </item>
        <item>
            <title>Serum myeloperoxidase levels and platelet activation parameters as diagnostic and prognostic markers in the course of coronary disease.</title>
            <link>http://www.medworm.com/index.php?rid=3343065&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20201999%26dopt%3DAbstract</link>
            <description>Authors: Pawlus J, Ho&amp;#x142;ub M, Ko&amp;#x17C;uch M, D&amp;#x105;browska M, Dobrzycki S
    Summary Early prediction of coronary artery disease complications is vital for the prevention and effective treatment of patients with coronary cardiac disease. It has been reported that inflammatory markers play a key role in the progression of cardiovascular diseases. Platelet count and platelet morphological parameters were analyzed on a fully-automated hematological analyzer ADVIA 2120 (Siemens). Serum myeloperoxidase (MPO) level was determined with an enzyme immunoassay (BioCheck). The measuring range of this assay is between 0 and 40 ng/ml. We demonstrate that serum MPO concentration and platelet activation increase systematically with the advancement of coronary artery disease. Moreover, MPO level i...</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3343065</comments>
            <pubDate>Thu, 25 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3343065</guid>        </item>
        <item>
            <title>The value of the Thomas-plot in the diagnostic work up of anemic patients referred by general practitioners.</title>
            <link>http://www.medworm.com/index.php?rid=3313299&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20175793%26dopt%3DAbstract</link>
            <description>In this study, we assessed the diagnostic value of the so-called Thomas'-plot [soluble transferrin receptor (sTfR)/log ferritin (sTfr/log Ferr) and the reticulocyte hemoglobin equivalent (Ret-HE)] in the anemia work up of patients referred by general practitioners. During July 2008-March 2009, 337 consecutive patients were included because of lowered Hb values. The laboratory results of the first 133 consecutive patients were used to determine the cut-off values for the diagnostic plot. The laboratory results of these patients were assessed and interpreted independently by two investigators, blinded from sTfR/log Ferr and Ret-HE values. The following 204 patients were used to test the plot in practice. In 32% of the first 133 patients, no indication of the cause of anemia could be found. H...</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3313299</comments>
            <pubDate>Wed, 17 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3313299</guid>        </item>
        <item>
            <title>Production of Interleukin-10 in serum and erythropoietin sensitivity in ESRD patients on hemodialysis.</title>
            <link>http://www.medworm.com/index.php?rid=3270360&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20148986%26dopt%3DAbstract</link>
            <description>Authors: Attia FM, Tawfik GA, Kalil KA, Mossalam MF
    Summary One of the clinical consequences of aberrant cytokines production in patients with end stage renal disease (ESRD) may be impaired erythropoiesis. To determine the interleukin (IL)-10 levels in ESRD patients on regular hemodialysis (HD) with good and poor response to recombinant human erythropoietin (Epo). Two groups of ESRD-HD patients were evaluated; 48 high epo HD patients and 32 low epo HD patients were evaluated for some laboratory tests and Interleukin-10 by ELISA. The production of IL-10 is decreased in HD with low epo group than high epo group 32.4 +/- 7.9 vs. 45 +/- 6.9 pg/ml (P &amp;lt; 0.001). IL-10 level is well correlated with CRP, ESR, Ferritin, Epo dose, and EPO/Hb ratio in ESRD-HD patients. These findings suggest th...</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3270360</comments>
            <pubDate>Tue, 09 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3270360</guid>        </item>
        <item>
            <title>Comparison of a point of care device against current laboratory methodology using citrated and EDTA samples for the determination of D-dimers in the exclusion of proximal deep vein thrombosis.</title>
            <link>http://www.medworm.com/index.php?rid=3270359&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20148987%26dopt%3DAbstract</link>
            <description>Conclusion: The Biosite Triage D-dimer assay performed on either citrate or EDTA samples is comparable with the Stago Liatest laboratory D-dimer assay when used in conjunction with clinical pretest probability scoring and CUS for the exclusion of DVT.
    PMID: 20148987 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3270359</comments>
            <pubDate>Tue, 09 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3270359</guid>        </item>
        <item>
            <title>Are 10 min of seating enough to guarantee stable haemoglobin and haematocrit readings for the athlete's biological passport?</title>
            <link>http://www.medworm.com/index.php?rid=3270358&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20148988%26dopt%3DAbstract</link>
            <description>Authors: Ahlgrim C, Pottgiesser T, Robinson N, Sottas PE, Ruecker G, Schumacher YO
    Summary Haemoglobin (Hb) and haematocrit (Hct) are measured as indirect markers of doping in athletes. We studied the effect of posture on these parameters in a typical antidoping setting. Venous blood samples were obtained from nine endurance athletes (six males, three females) and nine control subjects (six males, three females) immediately and after 5, 10, 15, 20 and 30 min after having adopted a seated position from normal daily activity. Hb (CV 0.72%) and Hct (CV 0.87%) were determined using an automated cell counter, plasma volume changes were calculated. Differences between the time points, gender and groups were calculated using a mixed-model procedure. Significant changes were observed in the fi...</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3270358</comments>
            <pubDate>Tue, 09 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3270358</guid>        </item>
        <item>
            <title>A novel homozygous point mutation at codon 82 (HBB:c.247A &gt; T)) in the beta-globin gene leads to thalassemia major.</title>
            <link>http://www.medworm.com/index.php?rid=3265728&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20136848%26dopt%3DAbstract</link>
            <description>Authors: Angalena R, Prabitha KN, Chaudhary AK, Bashyam MD, Jain S, Dalal AB
    
    PMID: 20136848 [PubMed - as supplied by publisher] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3265728</comments>
            <pubDate>Tue, 02 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3265728</guid>        </item>
        <item>
            <title>Evaluation of mean sphered corpuscular volume for predicting hereditary spherocytosis.</title>
            <link>http://www.medworm.com/index.php?rid=3265727&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20136849%26dopt%3DAbstract</link>
            <description>Authors: Bros&amp;#xE9;us J, Visomblain B, Guy J, Maynadi&amp;#xE9; M, Girodon F
    Summary Hereditary spherocytosis (HS) is a common red blood cell disorder. It has been shown that the mean sphered corpuscular volume (MSCV), an artificial volume, is always lower than the MCV in HS and also in some autoimmune haemolytic anaemia (AIHA). Our purpose was to assess the reliability of MSCV in routine practise, and its relevance in screening for HS. Comparison of MSCV and MCV was undertaken in a prospective study of 366 patients with anaemia. In addition, included were patients previously diagnosed to have HS (n = 33) or AIHA (n = 16). When MSCV was lower than MCV, a flow cytometric (FC) test for HS was performed. Delta (MCV-MSCV) values &amp;gt;9.6 fl were obtained for all HS patients. A wider spread of d...</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3265727</comments>
            <pubDate>Tue, 02 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3265727</guid>        </item>
        <item>
            <title>Evaluation of the CellaVision DM automated microscope in pediatrics.</title>
            <link>http://www.medworm.com/index.php?rid=3247420&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20132350%26dopt%3DAbstract</link>
            <description>Authors: Billard M, Lainey E, Armoogum P, Alberti C, Fenneteau O, DA Costa L
    Summary The DM is an automated microscope, which performs WBC differential counts and monitors red cell morphology. The user either validates the cell recognition if the DM has correctly identified the WBCs or reclassifies the WBCs in the good category in case of a DM mis-assignment. Morphological anomalies of leukocytes, red blood cells or platelets are analyzed and registered. We studied 521 newborns and infants sorted by age and pathology. The results correlated well with those using conventional microscopy except for samples containing blasts, in which the percentage of malignant cells was underestimated. Newborns had the lowest rates of overall accuracy and postclassification agreement. For red cell analy...</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3247420</comments>
            <pubDate>Tue, 02 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3247420</guid>        </item>
        <item>
            <title>Flow cytometric detection of circulating endothelial cells and endothelial progenitor cells in healthy subjects.</title>
            <link>http://www.medworm.com/index.php?rid=3198260&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20088999%26dopt%3DAbstract</link>
            <description>This study aimed to develop a flow cytometric (FCM) method for the immunophenotipic detection and enumeration of these cells in a healthy population. Peripheral blood samples from 32 subjects were analysed. Multiparameter FCM analysis was used to quantify resting and activated CEC and CEP. The mean values of the percentage and of the absolute number were: 0.005 +/- 0.004% and 306 +/- 243 cells/ml for CEC; 0.002 +/- 0.001% and 130 +/- 110 cells/ml for rCEC; 0.003 +/- 0.002% and 176 +/- 150 cells/ml for aCEC; 0.0001 +/- 0.00005% and 6 +/- 2 for CEP. We confirmed that FCM is an accurate and sensitive method for the quantitative analysis of CEC and CEP. The determination of normal ranges of CEC and CEP is helpful in defining their role as surrogate biomarkers of antiangiogenic treatment effica...</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3198260</comments>
            <pubDate>Sat, 23 Jan 2010 02:16:11 +0100</pubDate>
            <guid isPermaLink="false">3198260</guid>        </item>
        <item>
            <title>Multiplex fluorescence in situ hybridization in identifying chromosome involvement of complex karyotypes in de novo myelodysplastic syndromes and acute myeloid leukemia.</title>
            <link>http://www.medworm.com/index.php?rid=3198259&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20089000%26dopt%3DAbstract</link>
            <description>In this study, M-FISH was used in 16 patients with de novo MDS and 22 with AML with CCA detected by R-banding CC, and revealed 206 aberrations involved all 24 chromosomes, including 73 numerical chromosomal abnormalities and 133 structural abnormalities. The chromosomes most often involved were, by decreasing incidence, 5, 17, 8, 11, 7 and 21 in 57.9%, 55.3%, 44.7%, 36.8%, 34.2% and 34.2% of the cases, respectively. There were 98 unbalanced translocations, which were the most frequently observed aberrations in our study. Derivative chromosome 5 and 8 were implicated most often. The other derivatives were der(11), der(12), der(7), der(14), der(15) and der(17). Fourteen balanced translocations were detected in our series, and the most frequent reciprocal translocations was t(8;21). Fifty-fiv...</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3198259</comments>
            <pubDate>Sat, 23 Jan 2010 02:16:08 +0100</pubDate>
            <guid isPermaLink="false">3198259</guid>        </item>
        <item>
            <title>Laboratory findings in CD4(+) large granular lymphocytoses.</title>
            <link>http://www.medworm.com/index.php?rid=3198258&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20089001%26dopt%3DAbstract</link>
            <description>We report the clinicopathologic features of eight patients with aberrant CD4(+), cytotoxic T-cell lymphocytoses. Median follow-up was 29 months (range 8-100), during which all were alive without requirement for therapy. Four of eight patients had an additional malignancy; none had a history of rheumatoid arthritis, lymphadenopathy or hepatosplenomegaly. Morphologic expansions of granulated lymphocytes were evident in 6/8. All had immunophenotypically aberrant populations of CD4(+) T cells with uniform, moderate or bright CD56. Seven of eight expressed CD57, and four were CD8(partial dim +). Abnormal levels of expression of two or more T-cell antigens were seen in all cases. All tested cases were Tgamma PCR positive. Our results support that CD4(+) T-LGL lymphocytosis is a clonal disorder w...</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3198258</comments>
            <pubDate>Sat, 23 Jan 2010 02:16:05 +0100</pubDate>
            <guid isPermaLink="false">3198258</guid>        </item>
        <item>
            <title>Role of mean platelet volume as discriminating guide for bone marrow disease in patients with thrombocytopenia.</title>
            <link>http://www.medworm.com/index.php?rid=3174754&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20067547%26dopt%3DAbstract</link>
            <description>This study was conducted to analyze the role of mean platelet volume (MPV) as a guide or an indicator for bone marrow disease in thrombocytopenic patients. All the patients with thrombocytopenia for various causes followed by bone marrow examination were divided into two groups, one group with and another without bone marrow disease, depending on pathophysiology. The MPV was statistically analyzed in both the groups to assess its role as guide for bone marrow disease in these patients. Mean MPV (average score of all individual mean values in patients) in the group with bone marrow disease was 7.3 fl, while in the group without bone marrow disease, it was 8.62 fl. Although the difference in MPV in the two groups of with (including megaloblastic anemia) and without bone marrow involvement wa...</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3174754</comments>
            <pubDate>Mon, 11 Jan 2010 00:00:00 +0100</pubDate>
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            <title>Myelodysplastic syndrome in elderly patients: correlation of CBC with cytogenetic and FISH analysis.</title>
            <link>http://www.medworm.com/index.php?rid=3136417&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20041967%26dopt%3DAbstract</link>
            <description>Authors: Codispoti KE, Depalma L
    Summary Unexplained anemia in the elderly could represent myelodysplastic syndrome (MDS). We assessed the utility of using a fluorescence in situ hybridization (FISH) panel for common chromosomal abnormalities seen in MDS. A total of 101 elderly outpatients with anemia of unknown etiology were evaluated. Complete blood count, bone marrow biopsy, conventional cytogenetic analysis (CC), and FISH panel were reviewed. A total of 21 (21%) of the 101 patients had MDS. A combination of CC and FISH identified chromosomal abnormalities in 17 (81%) of the patients with MDS. The remaining 4 (19%) were diagnosed with MDS based solely on morphologic criteria. Except in two cases, FISH did not reveal abnormalities not already detected by CC. Furthermore, MDS patients...</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3136417</comments>
            <pubDate>Wed, 23 Dec 2009 00:00:00 +0100</pubDate>
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        <item>
            <title>Under-filled blood collection tubes containing KEDTA as anticoagulant are acceptable for automated complete blood counts, white blood cell differential, and reticulocyte count.</title>
            <link>http://www.medworm.com/index.php?rid=3136416&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20041968%26dopt%3DAbstract</link>
            <description>Authors: Xu M, Robbe VA, Jack RM, Rutledge JC
    Summary Current laboratory standards from Clinical Laboratory Standards Institute (CLSI) and manufacturer's (Becton Dickinson) data indicate that under-filling K(2)EDTA blood collection tubes can result in erroneous hematology values. To accommodate under-filled tubes and reduce collection volumes while optimizing our automation, we explored the acceptable limit of under-filled tubes for hematology values. We collected 8.0 ml of blood from 30 normal adult volunteers. Each donation was aliquoted in the following volumes: 4.0, 2.0, 1.0, 0.5 ml x 2. These samples were analyzed within 1 h of blood collection on Sysmex XE-2100 (Sysmex America Inc., Mundelein, IL, USA) for complete blood count, reticulocyte, and white blood cell differentials. Re...</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3136416</comments>
            <pubDate>Wed, 23 Dec 2009 00:00:00 +0100</pubDate>
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        <item>
            <title>Age-related plasma reference ranges for two heparin-binding proteins--vitronectin and platelet factor 4.</title>
            <link>http://www.medworm.com/index.php?rid=3004793&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19909382%26dopt%3DAbstract</link>
            <description>This study was conducted to establish age-related reference ranges for two heparin-binding proteins--vitronectin and platelet factor 4 (PF4)--and to determine if the quantitative values of these proteins may contribute to the reported age-dependent effect of unfractionated heparin (UFH). Plasma samples were obtained from healthy children aged between 1 month and 16 years and from healthy adult volunteers. Two commercial kits were used to measure plasma vitronectin and PF4 levels. Results were reported as mean and boundaries including 95% of the population. Plasma vitronectin levels for children aged 1-5 years were significantly higher compared with adults. Plasma PF4 levels for infants &amp;lt;1 year of age were significantly lower compared with adults. The differences between reference values...</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3004793</comments>
            <pubDate>Thu, 19 Nov 2009 04:32:08 +0100</pubDate>
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            <title>Evaluation of mean platelet volume in the differential diagnosis of thrombocytopenia.</title>
            <link>http://www.medworm.com/index.php?rid=3004792&amp;cid=s_36719_19_f&amp;fid=36719&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19909383%26dopt%3DAbstract</link>
            <description>Authors: Ntaios G, Papadopoulos A, Chatzinikolaou A, Girtovitis F, Kaiafa G, Savopoulos C, Hatzitolios A
    
    PMID: 19909383 [PubMed - in process] (Source: International Journal of Laboratory Hematology)</description>
            <author>International Journal of Laboratory Hematology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3004792</comments>
            <pubDate>Thu, 19 Nov 2009 04:32:05 +0100</pubDate>
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