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Blood|May 1, 1988
Hemostatic enzyme generation in the blood of patients with hereditary protein C deficiencyK A Bauer, A W Broekmans, R M Bertina, et al.
American Journal of Hematology|February 1, 1983
Familial and constitutional bleeding disorder due to platelet cyclo-oxygenase deficiencyM H Horellou, T Lecompte, C Lecrubier, et al.
Annales De Medecine Interne|January 1, 1989
[AL amyloidosis and primary fibrinolysis. Study of the mechanism of fibrinolysis]P Boudes, M H Horellou, O Bletry, et al.
Haemostasis|July 1, 1997
Vitamin K metabolism in a patient resistant to vitamin K antagonistsA Keréveur, M Leclercq, M Trossaërt, et al.
Thrombosis Research|November 5, 2002
Markers of activated coagulation in patients with factor V Leiden and/or G20210A prothrombin gene mutationI Gouin-Thibault, R Arkam, S Nassiri, et al.
Thrombosis Research. Supplement|January 1, 1991
Anti Xa activity and prothrombinase inhibition in patients treated with two different doses of enoxaparin in gynecologic surgeryM M Samama, S Combe, M H Horellou, et al.
American Journal of Hematology|June 1, 1992
Acquired von Willebrand disease: correction of hemostatic defect by high-dose intravenous immunoglobulinsA Delmer, M H Horellou, J M Bréchot, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|October 1, 1986
[Tissue plasminogen activator (t-PA) in myocardial infarction. Biological aspects]M Samama, E Verdy, J Conard, et al.
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