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Journal of Clinical Pathology|April 1, 1975
Detection of heterozygotes in both parents of homozygous patients with Von Willebrand's diseaseY Sultan, J Simeon, J P CaenThe Journal of Laboratory and Clinical Medicine|February 1, 1976
Electrophoretic heterogeneity of normal factor VIII/Von Willebrand protein, and abnormal electrophoretic mobility in patients with Von Willebrand's diseaseY Sultan, J Simeon, J P CaenThrombosis and Haemostasis|February 29, 1976
Immunologic studies in von Willebrand's disease: alteration of factor VIII/von Willebrand protein after transfusion with plasma concentrates in patients with von Willebrand's diseaseY Sultan, J Simeon, P Maisonneuve, et al.British Medical Journal|September 11, 1976
Bleeding in renal failure: a possible causeM Kazatchkine, Y Sultan, J P Caen, et al.Blood|April 1, 1978
Platelet factor VIII-related antigen: studies in vivo after transfusion in patients with von Willebrand diseaseY Sultan, C Jeanneau, J Lamaziere, et al.Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|January 1, 1985
[Paris-I-Lariboisière variant thrombasthenia. Functional disorder of human platelet aggregation, glycoprotein-independent]J P CaenThrombosis and Haemostasis|April 8, 1988
A randomized double-blind study between a low molecular weight heparin Kabi 2165 and standard heparin in the prevention of deep vein thrombosis in general surgery. A French multicenter trialJ P CaenThe Journal of Laboratory and Clinical Medicine|April 1, 1976
Bernard-Soulier syndrome: a new platelet glycoprotein abnormality. Its relationship with platelet adhesion to subendothelium and with the factor VIII von Willebrand proteinJ P Caen, A T Nurden, C Jeanneau, et al.Comptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales|January 1, 1992
[Platelets and aging]S Bellucci, J P CaenHaemostasis|January 1, 1976
Binding of 14C-ADP by thrombasthenic platelet membranesC Legrand, J P CaenPageof 36