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Revue Francaise De Transfusion Et Immuno-Hematologie|June 1, 1984
[Preparation of a specific anti-cytomegalovirus immunoglobulin for intravenous injection]M Maniez-Montreuil, M V Dupressoir-Burlet, L Martinache, et al.Vox Sanguinis|January 1, 1991
In vitro evaluation of a very-high-purity, solvent/detergent-treated, von Willebrand factor concentrateC Mazurier, S Jorieux, C de Romeuf, et al.Nouvelle Revue Francaise D'Hematologie|January 1, 1979
[Detection of platelet antibodies in idiopathic thrombocytopenic purpura (author's transl)]J Goudemand, M T Caulier, F Bauters, et al.Revue Francaise De Transfusion Et Immuno-Hematologie|June 1, 1981
Blood group A and B activity associated with factor VIII - von Willebrand factorC Mazurier, B Samor, L Mannessier, et al.Human Genetics|January 28, 1976
Hereditary hemolytic anemia with erythrocyte phosphofructokinase deficiency: studies of some properties of erythrocyte and muscle enzymeJ Etiemble, A Kahn, P Boivin, et al.Thrombosis and Haemostasis|June 3, 1987
Characterisation of a monoclonal antibody to von Willebrand factor as a potent inhibitor of ristocetin-mediated platelet interaction and platelet adhesionS Jorieux, C de Romeuf, B Samor, et al.Nouvelle Revue Francaise D'Hematologie|January 1, 1982
[Treatment of idiopathic thrombopenic purpura. Results obtained in a series of 219 cases]J Goudemand, A Marey, M T Caulier, et al.The FEBS Journal|April 4, 2008
Chemical approaches to mapping the function of post-translational modificationsDavid P Gamblin, Sander I van Kasteren, Justin M Chalker, et al.British Journal of Haematology|November 1, 1990
Evidence for a von Willebrand factor defect in factor VIII binding in three members of a family previously misdiagnosed mild haemophilia A and haemophilia A carriers: consequences for therapy and genetic counsellingC Mazurier, C Gaucher, S Jorieux, et al.Thrombosis and Haemostasis|December 19, 1980
Acquired von Willebrand's syndrome in the course of Waldenström's diseaseC Mazurier, A Parquet-Gernez, J Descamps, et al.Pageof 13