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Journal of Thrombosis and Haemostasis : JTH|June 18, 2010
Inactivation of ADAMTS13 by plasmin as a potential cause of thrombotic thrombocytopenic purpuraH B Feys, N Vandeputte, R Palla, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|October 10, 2013
Pregnancy complications and obstetric care in women with inherited bleeding disordersR A Kadir, J Davies, R Winikoff, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|June 9, 2017
Involvement of the IgE-basophil system and mild complement activation in haemophilia B with anti-factor IX neutralizing antibodies and anaphylaxisM Cugno, M E Mancuso, A Tedeschi, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|December 16, 2014
Research in haemophilia B--approaching the request for high evidence levels in a rare diseaseK Berger, D Schopohl, A Hilger, et al.
Vox Sanguinis|September 16, 2010
The effect of prion reduction in solvent/detergent-treated plasma on haemostatic variablesA S Lawrie, L Green, M T Canciani, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|February 19, 2014
Integrated postural analysis in children with haemophiliaE Boccalandro, G Pasta, P M Mannucci, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|April 13, 2017
Kreuth IV: European consensus proposals for treatment of haemophilia with coagulation factor concentratesP L F Giangrande, F Peyvandi, B O'Mahony, et al.
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