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Haemophilia : the Official Journal of the World Federation of Hemophilia|June 12, 2010
Factor VIII-specific B cell responses in haemophilia A patients with inhibitorsP M W van Helden, S D Van Haren, K Fijnvandraat, et al.
Lupus|August 1, 1996
Factor V Arg506-->Gln mutation in patients with antiphospholipid antibodiesB Montaruli, A Borchiellini, G Tamponi, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 13, 2009
Discordant antibody response in monozygotic twins with severe haemophilia A caused by intensive treatmentS C Gouw, P C ter Avest, P M van Helden, et al.
European Journal of Haematology|July 1, 1996
Arterial and venous thrombosis in two Italian families with the factor V Arg506-->Gln mutationB Montaruli, J Voorberg, G Tamponi, et al.
Journal of Thrombosis and Haemostasis : JTH|August 14, 2015
Angiogenic characteristics of blood outgrowth endothelial cells from patients with von Willebrand diseaseD J Groeneveld, T van Bekkum, R J Dirven, et al.
Journal of Thrombosis and Haemostasis : JTH|April 25, 2008
Covalent regulation of ULVWF string formation and elongation on endothelial cells under flow conditionsY Li, H Choi, Z Zhou, et al.
Blood|February 13, 2001
Multiple VH genes are used to assemble human antibodies directed toward the A3-C1 domains of factor VIIIE N van den Brink, E A Turenhout, N Bovenschen, et al.
Journal of Thrombosis and Haemostasis : JTH|August 22, 2012
Formation of platelet-binding von Willebrand factor strings on non-endothelial cellsJ W Wang, J A Valentijn, K M Valentijn, et al.
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