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Haemophilia : the Official Journal of the World Federation of Hemophilia|June 16, 2010
Persistent validity of a classification of congenital factor X defects based on clotting, chromogenic and immunological assays even in the molecular biology eraA Girolami, S Vettore, P Scarparo, et al.
Folia Haematologica (Leipzig, Germany : 1928)|January 1, 1985
Contact phase of coagulation in diabetes mellitus after aspirin administrationG M Patrassi, S Martinelli, A Picchinenna, et al.
Folia Haematologica (Leipzig, Germany : 1928)|January 1, 1988
Low incidence of familial occurrence of thrombocythaemia and/or thrombocytosisM L Randi, F Fabris, I Visentin, et al.
British Journal of Clinical Pharmacology|January 1, 1984
Effect of atenolol and metoprolol on the anticoagulant activity of acenocoumarinF Mantero, M Procidano, M A Vicariotto, et al.
Blut|July 1, 1983
A new family with classical factor X deficiency as demonstrated by electroimmunoassayA Girolami, G Luzzatto, N Scattolo, et al.
Clinical and Laboratory Haematology|January 1, 1982
Potentiation of anticoagulant response to warfarin by sulphinpyrazone: a double-blind study in patients with prosthetic heart valvesA Girolami, F Fabris, A Casonato, et al.
Haematologia|January 1, 1993
Bleeding as a cause of death in HIV-seropositive patients with congenital clotting disordersM Mares, M T Sartori, D Stocco, et al.
La Ricerca in Clinica E in Laboratorio|January 1, 1984
Are platelet factor 4 and beta-thromboglobulin markers of cardiovascular disorders?G Cella, N Scattolo, A Girolami, et al.
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