Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Stéphanie Martin-Blanc"'
Autor:
Bach-Nga Pham, Sandrine Kappler-Gratias, Dominique Gien, Isabelle Dubeaux, Sylvie Poupel, Geneviève Deram, Michèle Roussel, Thierry Peyrard, Philippe Rouger, Marylise Beolet, Stéphanie Martin-Blanc, Pierre-Yves Le Pennec, Geneviève Juszczak
Publikováno v:
Transfusion. 51:1249-1260
BACKGROUND: DNA testing has enabled the documenting of numerous variants of RHCE alleles, especially in individuals of African origin. The risk for production of clinically significant alloantibodies to Rh antigens of patients carrying variant RHCE a
Autor:
Stéphanie Martin-Blanc, P.-Y. Le Pennec, Sébastien Bourgouin, Maryline Ripaux, Philippe Rouger, Bach-Nga Pham, T. Peyrard
Publikováno v:
Transfusion Clinique et Biologique. 16:159-163
Resume But de l’etude La determination des antigenes erythrocytaires deduite de l’analyse des systemes de groupe sanguin par des techniques de biologie moleculaire (genotypage) est devenue en quelques annees un outil indispensable dans les labora
Autor:
Philippe Rouger, Stéphanie Martin-Blanc, P.Y. Le Pennec, Christophe Tournamille, J.-P. Cartron, Hélène Ansart-Pirenne
Publikováno v:
Vox Sanguinis. 92:142-147
Background and Objectives The Duffy (FY) blood group system is controlled by four major alleles: FY*A and FY*B, the Caucasian common alleles, encoding Fya and Fyb antigens; FY*X allele responsible for a poorly expressed Fyb antigen, and FY*Fy a silen
Autor:
Sandrine Kappler-Gratias, Dominique Gien, Stéphanie Martin-Blanc, Pierre-Yves Le Pennec, Bach-Nga Pham, Philippe Simon
Publikováno v:
Transfusion.
Background The Kell system, encoded by the KEL gene, is one of the most clinically important blood group systems. Molecular defects may lead to the absence of Kell antigen expression. The very rare KEL:5 results from silent KEL genes, also called KEL
Autor:
Stéphanie, Martin-Blanc, Philippe, Simon, Dominique, Gien, Sandrine, Kappler-Gratias, Pierre-Yves, Le Pennec, Bach-Nga, Pham
Publikováno v:
Transfusion. 53(11 Suppl 2)
The Kell system, encoded by the KEL gene, is one of the most clinically important blood group systems. Molecular defects may lead to the absence of Kell antigen expression. The very rare KEL:5 results from silent KEL genes, also called KELnull allele
Autor:
Bach-Nga, Pham, Thierry, Peyrard, Genevieve, Juszczak, Marylise, Beolet, Geneviève, Deram, Stéphanie, Martin-Blanc, Isabelle, Dubeaux, Michèle, Roussel, Sandrine, Kappler-Gratias, Dominique, Gien, Sylvie, Poupel, Philippe, Rouger, Pierre-Yves, Le Pennec
Publikováno v:
Transfusion. 51(6)
DNA testing has enabled the documenting of numerous variants of RHCE alleles, especially in individuals of African origin. The risk for production of clinically significant alloantibodies to Rh antigens of patients carrying variant RHCE alleles has l
Autor:
Stéphanie Martin-Blanc, Bach-Nga Pham, Pierre-Yves Le Pennec, Sandrine Kappler-Gratias, Philippe Bonin, Thierry Peyrard, Carine Auxerre, Sylvie Poupel, Philippe Rouger
Publikováno v:
Transfusion. 49(11)
BACKGROUND:ceAR (RHCE*ceAR) is a rare RH allele encountered in people of African/Caribbean ancestry, known to encode a partial e antigen. The homozygous ceAR/ceAR genotype encodes the rare blood group Hr−. This study describes alloanti-c/ce in a ce
Autor:
Stéphanie Martin-Blanc, Cédric Vrignaud, E. Gauthier, T. Peyrard, Joëlle Nataf, Michèle Roussel, Vincent Thonier
Publikováno v:
Transfusion Clinique et Biologique. 20:328