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Nouvelle Revue Francaise D'Hematologie|March 1, 1975
[Hereditary hypogranular thrombocytopathic thrombocytopenia. Ultrastructural study of a megakaryocytopathy (author's transl)]J Libánská, L Falcão, A Gautier, et al.
Presse Medicale (Paris, France : 1983)|January 15, 1983
[Molecular abnormalities in recurrent thromboembolic disease]E Dupuy, G Tobelem, C Soria, et al.
International Archives of Allergy and Applied Immunology|January 1, 1985
New functions for platelets and their pathological implicationsA Capron, J C Ameisen, M Joseph, et al.
The American Journal of Pathology|June 1, 1983
Evidence that abnormal platelet functions in human Chédiak-Higashi syndrome are the result of a lack of dense bodiesF Rendu, J Breton-Gorius, M Lebret, et al.
Journal of Thrombosis and Haemostasis : JTH|January 14, 2004
Fibrin polymerization is crucial for thrombin generation in platelet-rich plasma in a VWF-GPIb-dependent process, defective in Bernard-Soulier syndromeS Béguin, I Keularts, R Al Dieri, et al.
Blood|May 1, 1987
Heparin binding defect in a new antithrombin III variant: Rouen, 47 Arg to HisM C Owen, J Y Borg, C Soria, et al.
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