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Current Hematology Reports|September 1, 2005
Type 2N von Willebrand diseaseClaudine Mazurier, Lysiane Hilbert
Haematologica|September 21, 2004
A new candidate mutation, G1629R, in a patient with type 2A von Willebrand's disease: basic mechanisms and clinical implicationsLysiane Hilbert, Augusto B Federici, Luciano Baronciani, et al.
British Journal of Haematology|February 18, 2003
Two novel mutations, Q1053H and C1060R, located in the D3 domain of von Willebrand factor, are responsible for decreased FVIII-binding capacityLysiane Hilbert, Sylvie Jorieux, Valérie Proulle, et al.
International Journal of Hematology|February 15, 2002
Molecular genetics of type 2 von Willebrand diseaseEdith Fressinaud, Claudine Mazurier, Dominique Meyer
British Journal of Haematology|May 25, 2002
Large experience with a factor VIII binding assay of plasma von Willebrand factor using commercial reagentsClaudine Caron, Claudine Mazurier, Jenny Goudemand
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