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La Nouvelle Presse Medicale|June 13, 1981
[Acquired Willebrand factor deficiency associated with monoclonal IgG kappa gammapathy. Presence of an inhibitor of ristocetin co-factor (author's transl)]N Sitbon, M H Horellou, J Conard, et al.British Journal of Haematology|June 1, 1981
Constitutional thrombocytopathy with subnormal response to thromboxane A2M Samama, C Lecrubier, J Conard, et al.Blood|January 15, 1997
A single genetic origin for a common Caucasian risk factor for venous thrombosisA Zivelin, J H Griffin, X Xu, et al.Thrombosis Research|February 15, 1991
Fibrin-dependent fibrinolytic activity during extracorporeal circulationR Giuliani, E Szwarcer, E Martinez Aquino, et al.Thrombosis and Haemostasis|December 22, 1988
Coagulation assays as diagnostic markers of hepatocellular carcinomaJ J Lefrère, J Conard, P Mavier, et al.Presse Medicale (Paris, France : 1983)|November 14, 1987
[Hereditary protein S deficiency and recurrent venous thrombosis. Study of a family]A Bezeaud, L Venisse, J Conard, et al.Stroke|October 1, 1996
Coagulation studies, factor V Leiden, and anticardiolipin antibodies in 40 cases of cerebral venous thrombosisM A Deschiens, J Conard, M H Horellou, et al.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.American Journal of Hematology|August 1, 1986
A new case of high-molecular-weight kininogen inherited deficiencyJ J Lefrère, M H Horellou, D Gozin, et al.Pageof 92