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Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 1, 1994
First frameshift mutation in the active protein S gene associated with a quantitative hereditary deficiencyD Borgel, S Gandrille, M Gouault-Heilmann, et al.
Thrombosis and Haemostasis|December 1, 1995
Role of Fc gamma RIIA gene polymorphism in human platelet activation by monoclonal antibodiesC Bachelot, R Saffroy, S Gandrille, et al.
Thrombosis and Haemostasis|November 15, 1993
Compound heterozygosity in a family with protein C deficiency illustrating the complexity of the underlying molecular mechanismS Gandrille, B Jude, M Alhenc-Gelas, et al.
Presse Medicale (Paris, France : 1983)|September 24, 1994
[A new cause of familial thrombophilia: resistance to the effect of activated protein C]J Emmerich, M Alhenc-Gelas, S Gandrille, et al.
Nouvelle Revue Francaise D'Hematologie|January 1, 1992
Molecular abnormalities responsible for thrombosis. Genetic aspectsM Aiach, S Gandrille, J Emmerich, et al.
Thrombosis Research|October 29, 2000
Expression and characterization of recombinant protein S with the Ser 460 Pro mutationO Morboeuf, D Borgel, M Aiach, et al.
British Journal of Haematology|March 1, 1988
Association of inherited dysfibrinogenaemia and protein C deficiency in two unrelated familiesS Gandrille, P Priollet, L Capron, et al.
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