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British Journal of Haematology|June 3, 1999
Gly319 --> arg substitution in the dysfunctional prothrombin SegoviaS Akhavan, E Rocha, S Zeinali, et al.
Thrombosis and Haemostasis|August 1, 1995
Inhibitors to factor VIII in a family with mild hemophilia: molecular characterization and response to factor VIII and desmopressinE Santagostino, A Gringeri, L Tagliavacca, et al.
British Journal of Haematology|January 1, 1995
Factor VIII:C increases after desmopressin in a subgroup of patients with autosomal recessive severe von Willebrand diseaseG Castaman, A Lattuada, P M Mannucci, et al.
Haemostasis|January 1, 1982
Coagulation and platelet activation after retinal vein occlusionsD Mari, M Santori, G Bertoni, et al.
Acta Diabetologica Latina|July 1, 1981
Relationships between metabolic and hemostatic variables in uncomplicated diabetesC Vergani, G Bettale, D Mari, et al.
The Journal of Clinical Investigation|October 1, 1986
Binding of fibrinogen to human monocytesD C Altieri, P M Mannucci, A M Capitanio
British Journal of Haematology|March 1, 1992
Intramuscular anti-D immunoglobulins for home treatment of chronic immune thrombocytopenic purpuraA Gringeri, M Cattaneo, E Santagostino, et al.
Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontics|May 8, 2007
Oral surgery in patients on oral anticoagulant therapy: a randomized comparison of different intensity targetsR Sacco, M Sacco, M Carpenedo, et al.
British Journal of Haematology|August 1, 1986
von Willebrand factor contaminating porcine factor VIII concentrate (Hyate:C) causes platelet aggregationD C Altieri, A M Capitanio, P M Mannucci
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