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Antoine Hommais

Research Profile

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TOP 3
Antoine Hommais; Julie Rayes; Anne Houllier; Bernadette Obert; Paulette Legendre; Agnès Veyradier; Jean-Pierre Girma; Anne-Sophie Ribba
Molecular characterization of four ADAMTS13 mutations responsible for congenital thrombotic thrombocytopenic purpura (Upshaw-Schulman syndrome).
Julie Rayes; Antoine Hommais; Paulette Legendre; H Tout; Agnès Veyradier; Bernadette Obert; Anne-Sophie Ribba; Jean-Pierre Girma
Effect of von Willebrand disease type 2B and type 2M mutations on the susceptibility of von Willebrand factor to ADAMTS-13.
Antoine Hommais; Alain Stépanian; Edith Fressinaud; Claudine Mazurier; Katia Pouymayou; Dominique Meyer; Jean-Pierre Girma; Anne-Sophie Ribba
Impaired dimerization of von Willebrand factor subunit due to mutation A2801D in the CK domain results in a recessive type 2A subtype IID von Willebrand disease.

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All Publications

2007: Antoine Hommais; Julie Rayes; Anne Houllier; Bernadette Obert; Paulette Legendre; Agnès Veyradier; Jean-Pierre Girma; Anne-Sophie Ribba
Molecular characterization of four ADAMTS13 mutations responsible for congenital thrombotic thrombocytopenic purpura (Upshaw-Schulman syndrome).
Thrombosis and haemostasis 2007;98(3):593-9.
2007: Julie Rayes; Antoine Hommais; Paulette Legendre; H Tout; Agnès Veyradier; Bernadette Obert; Anne-Sophie Ribba; Jean-Pierre Girma
Effect of von Willebrand disease type 2B and type 2M mutations on the susceptibility of von Willebrand factor to ADAMTS-13.
Journal of thrombosis and haemostasis : JTH 2007;5(2):321-8.
2006: Antoine Hommais; Alain Stépanian; Edith Fressinaud; Claudine Mazurier; Katia Pouymayou; Dominique Meyer; Jean-Pierre Girma; Anne-Sophie Ribba
Impaired dimerization of von Willebrand factor subunit due to mutation A2801D in the CK domain results in a recessive type 2A subtype IID von Willebrand disease.
Thrombosis and haemostasis 2006;95(5):776-81.
2006: Antoine Hommais; A Stépanian; Edith Fressinaud; Claudine Mazurier; Dominique Meyer; Jean-Pierre Girma; Anne-Sophie Ribba
Mutations C1157F and C1234W of von Willebrand factor cause intracellular retention with defective multimerization and secretion.
Journal of thrombosis and haemostasis : JTH 2006;4(1):148-57.

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