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The Journal of Laboratory and Clinical Medicine|October 16, 1999
Antiphospholipid antibodies, proteins C and S, and coagulation changes in sickle cell diseaseM P Westerman, D Green, A Gilman-Sachs, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|October 7, 2017
Safety and dose-dependency of eptacog beta (activated) in a dose escalation study of non-bleeding congenital haemophilia A or B patients, with or without inhibitorsJ Ducore, J B Lawrence, M Simpson, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|December 9, 2017
Impact of pain and functional impairment in US adults with haemophilia: Patient-reported outcomes and musculoskeletal evaluation in the pain, functional impairment and quality of life (P-FiQ) studyC L Kempton, M Recht, A Neff, et al.Journal of Thrombosis and Haemostasis : JTH|August 29, 2018
Phase 1, single-dose escalating study of marzeptacog alfa (activated), a recombinant factor VIIa variant, in patients with severe hemophiliaR A Gruppo, D Malan, J Kapocsi, et al.Cancer Research|November 1, 1996
Human prostate carcinoma cells express enzymatic activity that converts human plasminogen to the angiogenesis inhibitor, angiostatinS Gately, P Twardowski, M S Stack, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|April 19, 2017
Self-reported prevalence, description and management of pain in adults with haemophilia: methods, demographics and results from the Pain, Functional Impairment, and Quality of life (P-FiQ) studyM Witkop, A Neff, T W Buckner, et al.Pageof 2