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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.Archiv Fur Geschwulstforschung|January 1, 1989
[Mitoguazone (methylglyoxal bis(guanylhydrazone))--its status and prospects]H Hoffmann, W Gutsche, R Amlacher, 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.Thrombosis and Haemostasis|February 12, 1999
Inhibitors in German hemophilia A patients treated with a double virus inactivated factor VIII concentrate bind to the C2 domain of FVIII light chainR Laub, M Di Giambattista, P Fondu, 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.Seminars in Oncology|April 1, 1992
A phase II trial of interferon alpha-2b with folinic acid and 5-fluorouracil administered by 4-hour infusion in metastatic colorectal carcinomaE D Kreuser, R U Hilgenfeld, M Matthias, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|February 28, 2004
Health status and health-related quality of life of children with haemophilia from six West European countriesA Gringeri, S von Mackensen, G Auerswald, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|February 9, 2007
Efficacy, safety and tolerability of recombinant factor VIII (REFACTO) in patients with haemophilia A: interim data from a postmarketing surveillance study in Germany and AustriaH Pollmann, D Externest, A Ganser, et al.Seminars in Thrombosis and Hemostasis|November 25, 2000
Molecular biology and clinical manifestation of hereditary factor VII deficiencyF H Herrmann, K Wulff, K Auberger, et al.Pageof 5