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Neurology|October 23, 2002
Clinical findings of a myoclonus-dystonia family with two distinct mutationsD Doheny, F Danisi, C Smith, et al.Thrombosis and Haemostasis|January 12, 2001
Congenital deficiency of vitamin K dependent coagulation factors in two families presents as a genetic defect of the vitamin K-epoxide-reductase-complexJ Oldenburg, B von Brederlow, A Fregin, et al.Hamostaseologie|November 8, 2011
Inhibitor-immunology-study. Evaluation of inhibitor development in haemophilia BI Wieland, C Wermes, B Eifrig, et al.Hamostaseologie|June 7, 2014
[Diagnosis of inherited diseases of platelet function. Interdisciplinary S2K guideline of the Permanent Paediatric Committee of the Society of Thrombosis and Haemostasis Research (GTH e. V.)]R Knöfler, W Eberl, H Schulze, et al.Clinical Immunology (Orlando, Fla.)|August 27, 2013
X-linked inhibitor of apoptosis (XIAP) deficiency: the spectrum of presenting manifestations beyond hemophagocytic lymphohistiocytosisC Speckmann, K Lehmberg, M H Albert, et al.Hamostaseologie|November 6, 2014
[Therapy of inherited diseases of platelet function. Interdisciplinary S2K guideline of the Permanent Paediatric Committee of the Society of Thrombosis and Haemostasis Research (GTH e. V.)]W Streif, R Knöfler, W Eberl, et al.Pageof 6