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Citation: L. Hilbert et al., Type 2M vWD resulting from a lysine deletion within a four lysine residue repeat in the A1 loop of von Willebrand factor, THROMB HAEM, 84(2), 2000, pp. 188-194

Authors: Lacquemant, C Gaucher, C Delorme, C Chatellier, G Gallois, Y Rodier, M Passa, P Balkau, B Mazurier, C Marre, M Froguel, P

Citation: C. Lacquemant et al., Association between high von Willebrand factor levels and the Thr789Ala VWF gene polymorphism but not with nephropathy in type 1 diabetes, KIDNEY INT, 57(4), 2000, pp. 1437-1443

Authors: Jorieux, S Fressinaud, E Goudemand, J Gaucher, C Meyer, D Mazurier, C

Citation: S. Jorieux et al., Conformational changes in the D ' domain of von Willebrand factor induced by CYS 25 and CYS 95 mutations lead to factor VIII binding defect and multimeric impairment, BLOOD, 95(10), 2000, pp. 3139-3145

Authors: Hilbert, L Gaucher, C Abgrall, JF Parquet, A Trzeciak, C Mazurier, C

Citation: L. Hilbert et al., Identification of new type 2B von Willebrand disease mutations: Arg543Gln,Arg545Pro and Arg578Leu, BR J HAEM, 103(3), 1998, pp. 877-884

Authors: Jorieux, S Gaucher, C Goudemand, J Mazurier, C

Citation: S. Jorieux et al., A novel mutation in the D3 domain of von Willebrand factor markedly decreases its ability to bind factor VIII and affects its multimerization, BLOOD, 92(12), 1998, pp. 4663-4670