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Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|July 1, 1993
A novel genetic thrombocytopenia (Paris-Trousseau) associated with platelet inclusions, dysmegakaryopoiesis and chromosome deletion AT 11q23R Favier, L Douay, B Esteva, et al.
Thrombosis Research|November 5, 2002
Markers of activated coagulation in patients with factor V Leiden and/or G20210A prothrombin gene mutationI Gouin-Thibault, R Arkam, S Nassiri, et al.
Thrombosis Research. Supplement|January 1, 1991
Anti Xa activity and prothrombinase inhibition in patients treated with two different doses of enoxaparin in gynecologic surgeryM M Samama, S Combe, M H Horellou, et al.
American Journal of Hematology|June 1, 1992
Acquired von Willebrand disease: correction of hemostatic defect by high-dose intravenous immunoglobulinsA Delmer, M H Horellou, J M Bréchot, et al.
Annales De Dermatologie Et De Venereologie|March 10, 2012
[Skin necrosis during long-term fluindione treatment revealing protein C deficiency]C Merklen-Djafri, I Mazurier, M-M Samama, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|January 1, 1987
[A specific marker of thrombolysis: DDE complex]J Soria, C Soria, M Mirshahi, et al.
Annales De Biologie Clinique|July 11, 2006
[A case of de novo acute basophilic leukaemia: diagnostic criteria and review of the literature]A Staal-Viliare, V Latger-Cannard, J P Rault, et al.
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