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British Journal of Haematology|September 1, 1992
Type IIB von Willebrand's disease: gene mutations and clinical presentation in nine families from Denmark, Germany and SwedenM Donnér, A C Kristoffersson, H Lenk, et al.
Journal of Pediatric Hematology/Oncology|February 24, 2001
Temporary response of localized intracranial mast cell sarcoma to combination chemotherapyP P Guenther, A Huebner, S B Sobottka, et al.
Archiv Fur Geschwulstforschung|January 1, 1989
[Mitoguazone (methylglyoxal bis(guanylhydrazone))--its status and prospects]H Hoffmann, W Gutsche, R Amlacher, et al.
Seminars in Thrombosis and Hemostasis|December 2, 1998
Molecular markers of the endothelium, the coagulation and the fibrinolytic systems in healthy newbornsR Knöfler, S Hofmann, G Weissbach, et al.
Annals of the New York Academy of Sciences|August 30, 2005
Inhibitor development in patients with hemophilia A after continuous infusion of FVIII concentratesCh von Auer, J Oldenburg, M von Depka, et al.
Seminars in Thrombosis and Hemostasis|May 25, 2001
Thrombolytic therapy in children--clinical experiences with recombinant tissue-plasminogen activatorR Knöfler, J Dinger, M Kabus, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|September 11, 2004
Treatment patterns and cost-of-illness of severe haemophilia in patients with inhibitors in GermanyG Auerswald, M von Depka Prondzinski, B Ehlken, et al.
Annals of Internal Medicine|July 1, 1990
Low risk for hepatitis C in hemophiliacs given a high-purity, pasteurized factor VIII concentrate. International Study GroupP M Mannucci, K Schimpf, D B Brettler, et al.
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