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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

246 related items for PubMed ID: 23362929

  • 21.
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  • 22. [Study on detection of samples of Rh-weak D and Del].
    Wang XZ, Lan JC, Wu XH, Zhou HY, Liu WJ, Liu D, Qi CS, Zeng FQ, Du KQ.
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2005 Jun; 13(3):509-11. PubMed ID: 15972154
    [Abstract] [Full Text] [Related]

  • 23. Serologic and molecular investigations of DAR1 (weak D Type 4.2), DAR1.2, DAR1.3, DAR2 (DARE), and DARA.
    Lejon Crottet S, Haer-Wigman L, Gowland P, Fontana S, Niederhauser C, Hustinx H.
    Transfusion; 2013 Nov; 53(11 Suppl 2):3000-8. PubMed ID: 23902153
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  • 24. Comprehensive analysis of RHD alleles in Argentineans with variant D phenotypes.
    Brajovich ME, Boggione CT, Biondi CS, Racca AL, Tarragó M, Nogués N, Muñiz-Díaz E, Cotorruelo CM.
    Transfusion; 2012 Feb; 52(2):389-96. PubMed ID: 21883261
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  • 28. RHD alleles among pregnant women with serologic discrepant weak D phenotypes from a multiethnic population and risk of alloimmunization.
    Bub CB, Aravechia MG, Costa TH, Kutner JM, Castilho L.
    J Clin Lab Anal; 2018 Jan; 32(1):. PubMed ID: 28374955
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  • 30. RHD genotyping and its implication in transfusion practice.
    Sassi A, Ouchari M, Houissa B, Romdhane H, Abdelkefi S, Chakroun T, Jemni Yacoub S.
    Transfus Apher Sci; 2014 Dec; 51(3):59-63. PubMed ID: 25457010
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  • 31. Resolving variable maternal D typing using serology and genotyping in selected prenatal patients.
    Clarke G, Hannon J, Berardi P, Barr G, Cote J, Fallis R, Alport T, Lane D, Petraszko T, Ochoa G, Goldman M.
    Transfusion; 2016 Dec; 56(12):2980-2985. PubMed ID: 27611891
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  • 32.
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  • 33. The determination of the fetal D status from maternal plasma for decision making on Rh prophylaxis is feasible.
    Müller SP, Bartels I, Stein W, Emons G, Gutensohn K, Köhler M, Legler TJ.
    Transfusion; 2008 Nov; 48(11):2292-301. PubMed ID: 18694461
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  • 34. How I manage donors and patients with a weak D phenotype.
    Flegel WA.
    Curr Opin Hematol; 2006 Nov; 13(6):476-83. PubMed ID: 17053462
    [Abstract] [Full Text] [Related]

  • 35. Serological weak D phenotypes: a review and guidance for interpreting the RhD blood type using the RHD genotype.
    Sandler SG, Chen LN, Flegel WA.
    Br J Haematol; 2017 Oct; 179(1):10-19. PubMed ID: 28508413
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  • 37. RHD allelic identification among D-Brazilian blood donors as a routine test using pools of DNA.
    Mota M, Dezan M, Valgueiro MC, Sakashita AM, Kutner JM, Castilho L.
    J Clin Lab Anal; 2012 Feb; 26(2):104-8. PubMed ID: 22467325
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  • 38. An easy RHD genotyping strategy for D- East Asian persons applied to Korean blood donors.
    Luettringhaus TA, Cho D, Ryang DW, Flegel WA.
    Transfusion; 2006 Dec; 46(12):2128-37. PubMed ID: 17176325
    [Abstract] [Full Text] [Related]

  • 39. Weak D phenotypes caused by intronic mutations in the RHD gene: four novel weak D alleles identified in the Chinese population.
    Ye L, He Y, Gao H, Guo Z, Zhu Z.
    Transfusion; 2013 Aug; 53(8):1829-33. PubMed ID: 23216299
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  • 40. Molecular background of D-negative phenotype in the Tunisian population.
    Moussa H, Tsochandaridis M, Chakroun T, Jridi S, Abdelneji B, Hmida S, Silvy M, Bailly P, Gabert J, Levy-Mozziconacci A, Jemni-Yacoub S.
    Transfus Med; 2012 Jun; 22(3):192-8. PubMed ID: 22420413
    [Abstract] [Full Text] [Related]

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