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J Astermark

Showing results (61-70 of 79) with videos related to

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Journal of Thrombosis and Haemostasis : JTH|November 25, 2003
Monitoring the bioavailability of FEIBA with a thrombin generation assayK Váradi, C Negrier, E Berntorp, et al.
Journal of Thrombosis and Haemostasis : JTH|June 12, 2014
The Fc gamma receptor IIa R131H polymorphism is associated with inhibitor development in severe hemophilia AC L Eckhardt, J Astermark, S Q Nagelkerke, et al.
Journal of Thrombosis and Haemostasis : JTH|January 16, 2009
Break-through bleeding in relation to predicted factor VIII levels in patients receiving prophylactic treatment for severe hemophilia AP W Collins, V S Blanchette, K Fischer, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|December 14, 2011
Treatment of haemophilia A and B and von Willebrand's disease: summary and conclusions of a systematic review as part of a Swedish health-technology assessmentE Berntorp, J Astermark, F Baghaei, et al.
Pathophysiology of Haemostasis and Thrombosis|July 11, 2003
Factor VIII inhibitor-bypassing agents act by inducing thrombin generation and can be monitored by a thrombin generation assayP L Turecek, K Váradi, B Keil, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|November 19, 2016
Anti-factor VIII antibodies in brothers with haemophilia A share similar characteristicsJ Kahle, A Orlowski, D Stichel, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|November 4, 2008
Factor VII deficiency: clinical manifestation of 717 subjects from Europe and Latin America with mutations in the factor 7 geneF H Herrmann, K Wulff, G Auerswald, et al.
Journal of Thrombosis and Haemostasis : JTH|October 3, 2003
Thrombosis in inherited factor VII deficiencyG Mariani, F H Herrmann, S Schulman, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|July 13, 2006
Current European practice in immune tolerance induction therapy in patients with haemophilia and inhibitorsJ Astermark, M Morado, A Rocino, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|July 14, 2005
Haemophilia Inhibitor Genetics Study - evaluation of a model for studies of complex diseases using linkage and association methodsE Berntorp, J Astermark, S M Donfield, et al.
Pageof 8

Showing results (61-70 of 79) with videos related to

Sort By:
Pageof 8
Journal of Thrombosis and Haemostasis : JTH|November 25, 2003
Monitoring the bioavailability of FEIBA with a thrombin generation assayK Váradi, C Negrier, E Berntorp, et al.
Journal of Thrombosis and Haemostasis : JTH|June 12, 2014
The Fc gamma receptor IIa R131H polymorphism is associated with inhibitor development in severe hemophilia AC L Eckhardt, J Astermark, S Q Nagelkerke, et al.
Journal of Thrombosis and Haemostasis : JTH|January 16, 2009
Break-through bleeding in relation to predicted factor VIII levels in patients receiving prophylactic treatment for severe hemophilia AP W Collins, V S Blanchette, K Fischer, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|December 14, 2011
Treatment of haemophilia A and B and von Willebrand's disease: summary and conclusions of a systematic review as part of a Swedish health-technology assessmentE Berntorp, J Astermark, F Baghaei, et al.
Pathophysiology of Haemostasis and Thrombosis|July 11, 2003
Factor VIII inhibitor-bypassing agents act by inducing thrombin generation and can be monitored by a thrombin generation assayP L Turecek, K Váradi, B Keil, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|November 19, 2016
Anti-factor VIII antibodies in brothers with haemophilia A share similar characteristicsJ Kahle, A Orlowski, D Stichel, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|November 4, 2008
Factor VII deficiency: clinical manifestation of 717 subjects from Europe and Latin America with mutations in the factor 7 geneF H Herrmann, K Wulff, G Auerswald, et al.
Journal of Thrombosis and Haemostasis : JTH|October 3, 2003
Thrombosis in inherited factor VII deficiencyG Mariani, F H Herrmann, S Schulman, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|July 13, 2006
Current European practice in immune tolerance induction therapy in patients with haemophilia and inhibitorsJ Astermark, M Morado, A Rocino, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|July 14, 2005
Haemophilia Inhibitor Genetics Study - evaluation of a model for studies of complex diseases using linkage and association methodsE Berntorp, J Astermark, S M Donfield, et al.
Pageof 8