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Items: 1 to 20 of 185

1.

Weak D and DEL alleles detected by routine SNaPshot genotyping: identification of four novel RHD alleles.

Silvy M, Simon S, Gouvitsos J, Di Cristofaro J, Ferrera V, Chiaroni J, Bailly P.

Transfusion. 2011 Feb;51(2):401-11. doi: 10.1111/j.1537-2995.2010.02830.x. Epub 2010 Aug 16.

PMID:
20723165
2.

RHD/CE typing by polymerase chain reaction using sequence-specific primers.

Gassner C, Schmarda A, Kilga-Nogler S, Jenny-Feldkircher B, Rainer E, Müller TH, Wagner FF, Flegel WA, Schönitzer D.

Transfusion. 1997 Oct;37(10):1020-6.

PMID:
9354819
3.

Weak D type 1.1 exemplifies another complexity in weak D genotyping.

Doescher A, Flegel WA, Petershofen EK, Bauerfeind U, Wagner FF.

Transfusion. 2005 Oct;45(10):1568-73.

PMID:
16181206
4.

Identification of RHD alleles with the potential of anti-D immunization among seemingly D- blood donors in Upper Austria.

Polin H, Danzer M, Gaszner W, Broda D, St-Louis M, Pröll J, Hofer K, Gabriel C.

Transfusion. 2009 Apr;49(4):676-81. doi: 10.1111/j.1537-2995.2008.02046.x. Epub 2009 Jan 2.

PMID:
19170995
5.

Effective molecular RHD typing strategy for blood donations.

Polin H, Danzer M, Hofer K, Gassner W, Gabriel C.

Transfusion. 2007 Aug;47(8):1350-5.

PMID:
17655577
6.

[Rh-D genotyping for exon 2, 5 and 7 of German and Japanese blood donors with sequence specific polymerase chain reaction].

Maas JH, Legler TJ, Lynen R, Blaschke V, Ohto H, Köhler M.

Beitr Infusionsther Transfusionsmed. 1997;34:203-9. German.

PMID:
9417341
7.

Molecular basis of the RHD gene in blood donors with DEL phenotypes in Shanghai.

Li Q, Hou L, Guo ZH, Ye LY, Yue DQ, Zhu ZY.

Vox Sang. 2009 Aug;97(2):139-46. doi: 10.1111/j.1423-0410.2009.01181.x. Epub 2009 Mar 30.

PMID:
19490579
8.

Molecular basis of weak D and DEL in Han population in Anhui Province, China.

Chen Q, Li M, Li M, Lu XS, Lü R, Sun J, Liu Z.

Chin Med J (Engl). 2012 Sep;125(18):3251-5.

PMID:
22964318
9.

Six years' experience performing RHD genotyping to confirm D- red blood cell units in Germany for preventing anti-D immunizations.

Flegel WA, von Zabern I, Wagner FF.

Transfusion. 2009 Mar;49(3):465-71. doi: 10.1111/j.1537-2995.2008.01975.x.

PMID:
19243542
10.

Random survey for RHD alleles among D+ European persons.

Chen Q, Flegel WA.

Transfusion. 2005 Jul;45(7):1183-91.

PMID:
15987365
11.

Molecular biology of partial D and weak D: implications for blood bank practice.

Flegel WA, Wagner FF.

Clin Lab. 2002;48(1-2):53-9. Review.

PMID:
11833677
12.

Novel weak D types 31 and 32: adsorption-elution-supported D antigen analysis and comparison to prevalent weak D types.

Körmöczi GF, Förstemann E, Gabriel C, Mayr WR, Schönitzer D, Gassner C.

Transfusion. 2005 Oct;45(10):1574-80.

PMID:
16181207
13.

Genotyping of RHD by multiplex polymerase chain reaction analysis of six RHD-specific exons.

Maaskant-van Wijk PA, Faas BH, de Ruijter JA, Overbeeke MA, von dem Borne AE, van Rhenen DJ, van der Schoot CE.

Transfusion. 1998 Nov-Dec;38(11-12):1015-21. Erratum in: Transfusion 1999 May;39(5):546.

PMID:
9838930
14.

RHD positive haplotypes in D negative Europeans.

Wagner FF, Frohmajer A, Flegel WA.

BMC Genet. 2001;2:10. Epub 2001 Jul 16.

15.

RHCE alleles detected after weak and/or discrepant results in automated Rh blood grouping of blood donors in Northern Germany.

Döscher A, Vogt C, Bittner R, Gerdes I, Petershofen EK, Wagner FF.

Transfusion. 2009 Sep;49(9):1803-11. doi: 10.1111/j.1537-2995.2009.02221.x. Epub 2009 May 18.

PMID:
19453979
16.

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.

PMID:
17176325
17.

Sensitive determination of the RhD genotype in mixed samples using fluorescence-based polymerase chain reaction.

Tonn T, Westrup D, Seidl C, Kirchmaier CM, Seifried E.

Vox Sang. 1997;72(3):177-81.

PMID:
9145489
18.

Identification of RHCE and KEL alleles in large cohorts of Afro-Caribbean and Comorian donors by multiplex SNaPshot and fragment assays: a transfusion support for sickle cell disease patients.

Silvy M, Di Cristofaro J, Beley S, Papa K, Rits M, Richard P, Chiaroni J, Bailly P.

Br J Haematol. 2011 Jul;154(2):260-70. doi: 10.1111/j.1365-2141.2011.08691.x. Epub 2011 May 28.

PMID:
21623766
19.

How I manage donors and patients with a weak D phenotype.

Flegel WA.

Curr Opin Hematol. 2006 Nov;13(6):476-83.

PMID:
17053462
20.

RHD gene polymorphisms among RhD-negative Chinese in Taiwan.

Sun CF, Chou CS, Lai NC, Wang WT.

Vox Sang. 1998;75(1):52-7.

PMID:
9745154

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