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Results: 1 to 20 of 98

Similar articles for PubMed (Select 23278863)

1.

Identification of novel polymorphism restricted to the (C)ces type 1 haplotype avoids risk of transfusion deadlock in SCD patients.

Silvy M, Granier T, Beley S, Chiaroni J, Bailly P.

Br J Haematol. 2013 Mar;160(6):863-7. doi: 10.1111/bjh.12179. Epub 2012 Dec 30. No abstract available.

PMID:
23278863
2.

Analysis of RhCE variants among 806 individuals in France: considerations for transfusion safety, with emphasis on patients with sickle cell disease.

Pham BN, Peyrard T, Juszczak G, Beolet M, Deram G, Martin-Blanc S, Dubeaux I, Roussel M, Kappler-Gratias S, Gien D, Poupel S, Rouger P, Le Pennec PY.

Transfusion. 2011 Jun;51(6):1249-60. doi: 10.1111/j.1537-2995.2010.02970.x. Epub 2010 Dec 16.

PMID:
21166680
3.

Molecular biology of the Rh system: clinical considerations for transfusion in sickle cell disease.

Chou ST, Westhoff CM.

Hematology Am Soc Hematol Educ Program. 2009:178-84. doi: 10.1182/asheducation-2009.1.178. Review.

4.

The role of molecular immunohematology in sickle cell disease.

Chou ST, Westhoff CM.

Transfus Apher Sci. 2011 Feb;44(1):73-9. doi: 10.1016/j.transci.2010.12.014. Epub 2011 Jan 28. Review.

PMID:
21277259
5.

High frequency of partial DIIIa and DAR alleles found in sickle cell disease patients suggests increased risk of alloimmunization to RhD.

Castilho L, Rios M, Rodrigues A, Pellegrino J Jr, Saad ST, Costa FF.

Transfus Med. 2005 Feb;15(1):49-55.

PMID:
15713129
6.

Molecular characterization of GYPB and RH in donors in the American Rare Donor Program.

Vege S, Westhoff CM.

Immunohematology. 2006;22(3):143-7.

PMID:
17105364
7.

RH genotyping in a sickle cell disease patient contributing to hematopoietic stem cell transplantation donor selection and management.

Fasano RM, Monaco A, Meier ER, Pary P, Lee-Stroka AH, Otridge J, Klein HG, Marincola FM, Kamani NR, Luban NL, Stroncek D, Flegel WA.

Blood. 2010 Oct 14;116(15):2836-8. doi: 10.1182/blood-2010-04-279372. Epub 2010 Jul 19.

8.

Rare RHCE phenotypes in black individuals of Afro-Caribbean origin: identification and transfusion safety.

Noizat-Pirenne F, Lee K, Pennec PY, Simon P, Kazup P, Bachir D, Rouzaud AM, Roussel M, Juszczak G, Ménanteau C, Rouger P, Kotb R, Cartron JP, Ansart-Pirenne H.

Blood. 2002 Dec 1;100(12):4223-31. Epub 2002 Aug 1.

9.

Partial C antigen in sickle cell disease patients: clinical relevance and prevention of alloimmunization.

Tournamille C, Meunier-Costes N, Costes B, Martret J, Barrault A, Gauthier P, Galactéros F, Nzouékou R, Bierling P, Noizat-Pirenne F.

Transfusion. 2010 Jan;50(1):13-9. doi: 10.1111/j.1537-2995.2009.02382.x. Epub 2009 Sep 22.

PMID:
19778340
10.

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
11.

The structure and function of the Rh antigen complex.

Westhoff CM.

Semin Hematol. 2007 Jan;44(1):42-50. Review.

12.

Weakened expression of 'e' owing to concomitant occurrence of Cys16 and Val245 (VS antigen).

Rodrigues A, Rios M, Costa FF, Saad ST, Pellegrino J Jr, Castilho L.

Vox Sang. 2004 Feb;86(2):136-40.

PMID:
15023184
13.

DNA-based typing of blood groups for the management of multiply-transfused sickle cell disease patients.

Castilho L, Rios M, Bianco C, Pellegrino J Jr, Alberto FL, Saad ST, Costa FF.

Transfusion. 2002 Feb;42(2):232-8.

PMID:
11896340
14.

Two molecular polymorphisms to detect the (C)ce(s) type 1 haplotype.

Flegel WA, Wagner FF.

Blood Transfus. 2014 Jan;12(1):136-7. doi: 10.2450/2013.0149-13. Epub 2013 Nov 15. No abstract available.

15.

Distribution of the FYBES and RHCE*ce(733C>G) alleles in an Argentinean population: implications for transfusion medicine.

Cotorruelo CM, Fiori SV, Borrás SE, Racca LL, Biondi CS, Racca AL.

BMC Med Genet. 2008 May 6;9:40. doi: 10.1186/1471-2350-9-40.

16.

The Rh and RhAG blood group systems.

Chou ST, Westhoff CM.

Immunohematology. 2010;26(4):178-86. Review. No abstract available.

PMID:
22356455
17.

Relevance of RH variants in transfusion of sickle cell patients.

Noizat-Pirenne F, Tournamille C.

Transfus Clin Biol. 2011 Dec;18(5-6):527-35. doi: 10.1016/j.tracli.2011.09.001. Epub 2011 Oct 22. Review.

PMID:
22024128
18.

The clinical impact of MTHFR polymorphism on the vascular complications of sickle cell disease.

Moreira Neto F, Lourenço DM, Noguti MA, Morelli VM, Gil IC, Beltrão AC, Figueiredo MS.

Braz J Med Biol Res. 2006 Oct;39(10):1291-5. Epub 2006 Aug 22.

19.

Polymorphisms associated with sickle cell disease in Southern Iran.

Haghpanah S, Nasirabadi S, Kianmehr M, Afrasiabi A, Karimi M.

Genetika. 2012 Jul;48(7):890-3.

PMID:
22988776
20.

On the benefit of blood group molecular genotyping in cord blood banking.

Sbarsi I, Bergamaschi P, Martinetti M, Salvaneschi L.

Vox Sang. 2009 Nov;97(4):360-1. doi: 10.1111/j.1423-0410.2009.01245.x. No abstract available.

PMID:
19840354
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