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Blood|July 6, 2022
Immune complications and their management in inherited and acquired bleeding disordersValder R Arruda, David Lillicrap, Roland W Herzog
Journal of Thrombosis and Haemostasis : JTH|May 18, 2024
Application of genetic testing for the diagnosis of von Willebrand diseaseOmid Seidizadeh, Luciano Baronciani, David Lillicrap, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|March 14, 2024
Diagnosis and treatment of von Willebrand disease in 2024 and beyondPaula James, Frank Leebeek, Caterina Casari, et al.
Research and Practice in Thrombosis and Haemostasis|February 18, 2026
Factor VIII in vitro bioequivalence of denecimig (Mim8) hemostatic effect by thrombin generation assaysJacob Lund, Mirella Ezban, Kasper Jensen, et al.
Blood|April 23, 2017
Biological considerations of plasma-derived and recombinant factor VIII immunogenicityJesse Lai, Christine Hough, Julie Tarrant, et al.
Expert Review of Hematology|March 19, 2020
Patients with hemophilia A and inhibitors: prevention and evolving treatment paradigmsDavid Lillicrap, Karin Fijnvandraat, Guy Young, et al.
Cellular Immunology|December 18, 2015
War and peace: Factor VIII and the adaptive immune responseMaria T Georgescu, Jesse D Lai, Christine Hough, et al.
Journal of Thrombosis and Haemostasis : JTH|August 11, 2022
Heterogeneity and reciprocity of FVIII and VWF expression, and the response to shear stress in cultured human endothelial cellsChristine Hough, Colleen Notley, Aomei Mo, et al.
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