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C Boyer-Neumann

Showing results (41-50 of 44) with videos related to

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Thrombosis and Haemostasis|October 18, 1993
Functional analysis of the Arg91Gln substitution in the factor VIII binding domain of von Willebrand factor demonstrates variable phenotypic expressionJ M Lavergne, Y Piao, A S Ribba, et al.
Journal of Acquired Immune Deficiency Syndromes|January 1, 1992
Endothelial cell dysfunction in HIV infectionA Lafeuillade, M C Alessi, I Poizot-Martin, et al.
Blood|February 13, 2001
The arginine-552-cysteine (R1315C) mutation within the A1 loop of von Willebrand factor induces an abnormal folding with a loss of function resulting in type 2A-like phenotype of von Willebrand disease: study of 10 patients and mutated recombinant von Willebrand factorA N Ribba, L Hilbert, J M Lavergne, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|March 31, 2015
Factor XI replacement for inherited factor XI deficiency in routine clinical practice: results of the HEMOLEVEN prospective 3-year postmarketing studyF Bauduer, E de Raucourt, C Boyer-Neumann, et al.
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Showing results (41-50 of 44) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 44 results.
Thrombosis and Haemostasis|October 18, 1993
Functional analysis of the Arg91Gln substitution in the factor VIII binding domain of von Willebrand factor demonstrates variable phenotypic expressionJ M Lavergne, Y Piao, A S Ribba, et al.
Journal of Acquired Immune Deficiency Syndromes|January 1, 1992
Endothelial cell dysfunction in HIV infectionA Lafeuillade, M C Alessi, I Poizot-Martin, et al.
Blood|February 13, 2001
The arginine-552-cysteine (R1315C) mutation within the A1 loop of von Willebrand factor induces an abnormal folding with a loss of function resulting in type 2A-like phenotype of von Willebrand disease: study of 10 patients and mutated recombinant von Willebrand factorA N Ribba, L Hilbert, J M Lavergne, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|March 31, 2015
Factor XI replacement for inherited factor XI deficiency in routine clinical practice: results of the HEMOLEVEN prospective 3-year postmarketing studyF Bauduer, E de Raucourt, C Boyer-Neumann, et al.
Pageof 5