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Journal of Thrombosis and Haemostasis : JTH|November 21, 2020
Factor VIII pharmacokinetics associates with genetic modifiers of VWF and FVIII clearance in an adult hemophilia A populationKenichi Ogiwara, Laura L Swystun, A Simonne Paine, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|October 23, 2020
The challenge of genetically unresolved haemophilia A patients: Interest of the combination of whole F8 gene sequencing and functional assaysFanny Lassalle, Yohann Jourdy, Loubna Jouan, et al.
Nucleic Acids Research|June 22, 2026
Leukemia risk factor ARID5B coordinates HDAC-mediated transcriptional repressionAna P Kutschat, Fabian Frommelt, Brianda L Santini, et al.
Thrombosis and Haemostasis|June 12, 2015
Diagnostic accuracy study of a factor VIII ELISA for detection of factor VIII antibodies in congenital and acquired haemophilia APaul Batty, Gary W Moore, Sean Platton, et al.
Blood Advances|January 12, 2022
Novel cysteine substitution p.(Cys1084Tyr) causes variable expressivity of qualitative and quantitative VWF defectsOrla Rawley, Laura L Swystun, Christine Brown, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|February 3, 2011
A microRNA-regulated and GP64-pseudotyped lentiviral vector mediates stable expression of FVIII in a murine model of Hemophilia AHideto Matsui, Carol Hegadorn, Margareth Ozelo, et al.
Journal of Thrombosis and Haemostasis : JTH|July 3, 2022
Longitudinal bleeding assessment in von Willebrand disease utilizing an interim bleeding scoreMichelle Lavin, Pamela Christopherson, Julie Grabell, et al.
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