Definitions in hemophilia: Recommendation of the scientific subcommittee on factor VIII and factor IX of the scientific and standardization committee of the International Society on Thrombosis and Hemostasis
White GC II, Rosendaal F, Aledort LM, et al. Definitions in hemophilia: recommendation of the scientific subcommittee on factor VIII and factor IX of the scientific and standardization committee of the International Society on Thrombosis and Hemostasis. Thromb Haemost. 2001;85: 560-568.
Guidelines on the selection and use of therapeutic products to treat hemophilia and other hereditary bleeding disorders
United Kingdom Haemophilia Centre Doctors' Organization. Guidelines on the selection and use of therapeutic products to treat hemophilia and other hereditary bleeding disorders. Haemophilia. 2003;9:1-23.
Human recombinant factor IX: Safety and efficacy studies in hemophilia B patients previously treated with plasma-derived factor IX concentrates
Roth DA, Kessler CM, Pasi J, et al. Human recombinant factor IX: safety and efficacy studies in hemophilia B patients previously treated with plasma-derived factor IX concentrates. Blood. 2001;98:3600-3606.
Discontinuation of prophylactic therapy in severe haemophilia: Incidence and effects on outcome
Fischer K, Van der bom JG, Prejs R. et al. Discontinuation of prophylactic therapy in severe haemophilia: incidence and effects on outcome. Haemophilia. 2001;7:544-550.
Prophylactic treatment for severe haemophilia: Comparison of an intermediate-dose to a high-dose regimen
Fischer K, Astermark J, Van der bom JG, et al. Prophylactic treatment for severe haemophilia: comparison of an intermediate-dose to a high-dose regimen. Haemophilia. 2002;8:753-760.