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Haemophilia : the Official Journal of the World Federation of Hemophilia|November 25, 2006
The epidemiology of factor VIII inhibitorsCharles R M HayBlood|November 22, 2011
The principal results of the International Immune Tolerance Study: a randomized dose comparisonCharles R M Hay, Donna M DiMichele, Journal of Thrombosis and Haemostasis : JTH|December 17, 2020
Mortality in congenital hemophilia A - a systematic literature reviewCharles R M Hay, Francis Nissen, Steven W PipeBritish Journal of Haematology|October 6, 2004
Acquired Glanzmann's thrombasthenia without thrombocytopenia: a severe acquired autoimmune bleeding disorderEleni Tholouli, Charles R M Hay, Peter O'Gorman, et al.Acute Medicine|January 15, 2016
Acquired haemophilia: an easy diagnosis to miss in a patient taking warfarinAvraneel Talapatra, Michael J Nash, Charles R M Hay, et al.British Journal of Haematology|May 18, 2006
The diagnosis and management of factor VIII and IX inhibitors: a guideline from the United Kingdom Haemophilia Centre Doctors OrganisationCharles R M Hay, S Brown, P W Collins, et al.Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 10, 2019
Perioperative laboratory monitoring in congenital haemophilia patients with inhibitors: a systematic literature reviewDaniel P Hart, Charles R M Hay, Ri Liesner, et al.Blood|April 26, 2015
Sample conditions determine the ability of thrombin generation parameters to identify bleeding phenotype in FXI deficiencyGillian N Pike, Anthony M Cumming, Charles R M Hay, et al.World Journal of Surgery|September 29, 2011
General surgery in patients with a bleeding diathesis: how we do itKamal R Aryal, D Wiseman, Ajith K Siriwardena, et al.Blood|April 8, 2011
Incidence of factor VIII inhibitors throughout life in severe hemophilia A in the United KingdomCharles R M Hay, Ben Palmer, Elizabeth Chalmers, et al.Pageof 3