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Thrombosis and Haemostasis|June 12, 1999
Longitudinal analysis of factor VIII inhibitors in a previously untreated mild haemophilia A patient with an Arg593-->Cys substitutionE N van den Brink, S M Timmermans, E A Turenhout, et al.
Lancet (London, England)|June 18, 1994
Association of idiopathic venous thromboembolism with single point-mutation at Arg506 of factor VJ Voorberg, J Roelse, R Koopman, et al.
British Journal of Haematology|October 29, 1998
Small GTP-binding proteins in human endothelial cellsH P de Leeuw, P M Koster, J Calafat, et al.
Blood|January 11, 2000
Human antibodies with specificity for the C2 domain of factor VIII are derived from VH1 germline genesE N van Den Brink, E A Turenhout, J Davies, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|December 21, 2000
Disappearance of factor VIII autoantibodies preceding autoimmune haemolytic anaemiaE N van den Brink, E A Turenhout, E C Wijn-Maas, et al.
Journal of Thrombosis and Haemostasis : JTH|November 29, 2013
Phosphatidylinositol-3,4,5-triphosphate-dependent Rac exchange factor 1 regulates epinephrine-induced exocytosis of Weibel-Palade bodiesK W E M van Hooren, D van Breevoort, M Fernandez-Borja, et al.
Molecular Biology of the Cell|November 10, 2000
Alternative splicing of the human Rab6A gene generates two close but functionally different isoformsA Echard, F J Opdam, H J de Leeuw, et al.
Journal of Thrombosis and Haemostasis : JTH|December 5, 2008
VH1-69 germline encoded antibodies directed towards ADAMTS13 in patients with acquired thrombotic thrombocytopenic purpuraW Pos, B M Luken, J A Kremer Hovinga, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 25, 2010
Domain specificity of factor VIII inhibitors during immune tolerance induction in patients with haemophilia AP M W van Helden, P H P Kaijen, E P Mauser-Bunschoten, et al.
Blood|April 18, 1998
A human alloantibody interferes with binding of factor IXa to the factor VIII light chainK Fijnvandraat, P H Celie, E A Turenhout, et al.
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