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Blood|February 24, 2006
Prothrombin 20210G>A is an ancestral prothrombotic mutation that occurred in whites approximately 24,000 years agoAriella Zivelin, Ronit Mor-Cohen, Victoria Kovalsky, et al.
Internal and Emergency Medicine|May 18, 2024
Bleeding and thrombotic events and intensity of heparin therapy in the two first waves of COVID-19Raffaella Rossio, Mauro Tettamanti, Alessia Antonella Galbussera, et al.
Thrombosis and Haemostasis|October 6, 2023
Clinical and Laboratory Presentation and Underlying Mechanism in Patients with Low VWFOmid Seidizadeh, Alessandro Ciavarella, Luciano Baronciani, et al.
Blood Advances|July 28, 2023
Residual burden of liver disease after HCV clearance in hemophilia: a word of caution in the era of gene therapyVincenzo La Mura, Niccolò Bitto, Cecilia Capelli, et al.
American Journal of Hematology|June 11, 2026
Clinical and Laboratory Characterization of Acquired Von Willebrand SyndromeAlessandro Ciavarella, Luciano Baronciani, Omid Seidizadeh, et al.
Thrombosis and Haemostasis|March 1, 2005
Clinical phenotypes and factor VII genotype in congenital factor VII deficiencyGuglielmo Mariani, Falko H Herrmann, Alberto Dolce, et al.
Journal of Thrombosis and Haemostasis : JTH|August 22, 2024
Gene therapy for people with hemophilia B: a proposed care delivery model in ItalyGiancarlo Castaman, Giovanni Di Minno, Paolo Simioni, et al.
Research and Practice in Thrombosis and Haemostasis|June 3, 2026
Real-world provider experiences with hemophilia A gene therapy: administration of valoctocogene roxaparvovecFlora Peyvandi, Robert Klamroth, Johannes Oldenburg, et al.
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