Hereditary Clotting Factor Deficiencies (Bleeding Disorders)
暂无分享,去创建一个
[1] M. Manco‐Johnson,et al. Athletic Participation in Severe Hemophilia: Bleeding and Joint Outcomes in Children on Prophylaxis , 2009, Pediatrics.
[2] A. Iorio,et al. Comparison of the rates of joint arthroplasty in patients with severe factor VIII and IX deficiency: an index of different clinical severity of the 2 coagulation disorders. , 2009, Blood.
[3] F. Peyvandi,et al. Factor V Deficiency , 2009, Seminars in thrombosis and hemostasis.
[4] R. De Cristofaro,et al. Congenital prothrombin deficiency. , 2009, Seminars in thrombosis and hemostasis.
[5] C. Hermans,et al. Replacement therapy for invasive procedures in patients with haemophilia: literature review, European survey and recommendations , 2009, Haemophilia : the official journal of the World Federation of Hemophilia.
[6] L. Almasy,et al. Inhibitors of factor VIII in black patients with hemophilia. , 2009, The New England journal of medicine.
[7] T. Kennedy-Martin,et al. A systematic review of the cost‐effectiveness of rFVIIa and APCC in the treatment of minor/moderate bleeding episodes for haemophilia patients with inhibitors , 2009, Haemophilia : the official journal of the World Federation of Hemophilia.
[8] S. L. Carpenter,et al. α2‐Antiplasmin and its deficiency: fibrinolysis out of balance , 2008, Haemophilia : the official journal of the World Federation of Hemophilia.
[9] R. Ljung,et al. Management of carriers and babies with haemophilia , 2008, Haemophilia : the official journal of the World Federation of Hemophilia.
[10] P. Mannucci,et al. Back to the future: a recent history of haemophilia treatment , 2008, Haemophilia : the official journal of the World Federation of Hemophilia.
[11] S. Pipe. Recombinant clotting factors , 2008, Thrombosis and Haemostasis.
[12] J. Saint-Remy,et al. The use of factor VIII/von Willebrand factor concentrate for immune tolerance induction in haemophilia A patients with high‐titre inhibitors: association of clinical outcome with inhibitor epitope profile , 2008, Haemophilia : the official journal of the World Federation of Hemophilia.
[13] B. Wiman,et al. Laboratory evidence of hyperfibrinolysis in association with low plasminogen activator inhibitor type 1 activity , 2007, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.
[14] Alan R. Cohen,et al. Prophylaxis versus episodic treatment to prevent joint disease in boys with severe hemophilia. , 2007, The New England journal of medicine.
[15] C. Négrier,et al. Coagulation factor concentrates: past, present, and future , 2007, The Lancet.
[16] U. Seligsohn,et al. Factor XI in haemostasis and thrombosis: Past, present and future , 2007, Thrombosis and Haemostasis.
[17] D. DiMichele. Immune tolerance: critical issues of factor dose, purity and treatment complications , 2006, Haemophilia : the official journal of the World Federation of Hemophilia.
[18] J. Astermark,et al. Inhibitor treatment in haemophilias A and B: summary statement for the 2006 international consensus conference , 2006, Haemophilia : the official journal of the World Federation of Hemophilia.
[19] E. Berntorp,et al. The von Willebrand disease prophylaxis network: exploring a treatment concept , 2006, Journal of thrombosis and haemostasis : JTH.