D Meyer

New variant of von Willebrand disease with defective binding to factor VIII

Masami Nishino, JP Girma, C Rothschild et al. · Blood · 1989 · 234 citations · Full text

Ten candidate ADAMTS13 mutations in six French families with congenital thrombotic thrombocytopenic purpura (Upshaw–Schulman syndrome)

Agnès Veyradier, J. M. Lavergne, Anne‐Sophie Ribba et al. · Journal of Thrombosis and Haemostasis · 2004 · 113 citations · Full text

French Families, Genetic Disorder, Genetics +8

The binding domain of von Willebrand factor to sulfatides is distinct from those interacting with glycoprotein Ib, heparin, and collagen and resides between amino acid residues Leu 512 and Lys 673

Olivier D. Christophe, Bernadette Obert, D Meyer et al. · Blood · 1991 · 54 citations · Full text

Mediation of platelet adhesion to fibrillar collagen in flowing blood by a proteolytic fragment of human von Willebrand factor

KS Sakariassen, E Fressinaud, JP Girma et al. · Blood · 1986 · 47 citations · Full text

Structural analysis of five lactose-containing oligosaccharides by improved, high-resolution, two-dimensional 1H-n.m.r. spectroscopy

N. Platzer, Daniel Davoust, Michel Lhermitte et al. · Carbohydrate Research · 1989 · 22 citations

Engineering, Biochemistry, Glycobiology +9