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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 HerzogJournal 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.Blood|March 7, 2024
Vector integration and fate in the hemophilia dog liver multiple years after AAV-FVIII gene transferPaul Batty, Sylvia Fong, Matteo Franco, et al.Journal of Thrombosis and Haemostasis : JTH|October 29, 2025
A comprehensive care pathway of gene therapy for hemophilia based on current guideline documents and summary of product characteristics: communication from the ISTH SSC working group on gene therapyCaroline M A Mussert, Wolfgang Miesbach, Pratima Chowdary, 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.Pageof 19