Prevalent inhibitors in haemophilia B subjects enrolled in the Universal Data Collection database
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J. Puetz | C. Kempton | P. Monahan | J. Soucie | J. M. Soucie | J. Puetz
[1] R. Presley,et al. Increased prevalence of inhibitors in Hispanic patients with severe haemophilia A enrolled in the Universal Data Collection database , 2012, Haemophilia : the official journal of the World Federation of Hemophilia.
[2] M. Recht,et al. A retrospective study to describe the incidence of moderate to severe allergic reactions to factor IX in subjects with haemophilia B , 2011, Haemophilia : the official journal of the World Federation of Hemophilia.
[3] Meredith A Oakley,et al. The universal data collection surveillance system for rare bleeding disorders. , 2010, American journal of preventive medicine.
[4] I. Warrier,et al. Inhibitors in factor IX deficiency a report of the ISTH‐SSC international FIX inhibitor registry (1997–2006) , 2009, Haemophilia : the official journal of the World Federation of Hemophilia.
[5] E. Santagostino,et al. Risk stratification for inhibitor development at first treatment for severe hemophilia A: a tool for clinical practice , 2008, Journal of thrombosis and haemostasis : JTH.
[6] P. Mannucci,et al. Factor VIII products and inhibitor development: the SIPPET study (survey of inhibitors in plasma‐product exposed toddlers) , 2007, Haemophilia : the official journal of the World Federation of Hemophilia.
[7] D. DiMichele. Inhibitor development in haemophilia B: an orphan disease in need of attention , 2007, British journal of haematology.
[8] J. Astermark. Why do inhibitors develop? Principles of and factors influencing the risk for inhibitor development in haemophilia , 2006, Haemophilia : the official journal of the World Federation of Hemophilia.
[9] T. Lambert,et al. Influence of the type of factor VIII concentrate on the incidence of factor VIII inhibitors in previously untreated patients with severe hemophilia A. , 2006, Blood.
[10] V. Blanchette,et al. The safety and efficacy of recombinant human blood coagulation factor IX in previously untreated patients with severe or moderately severe hemophilia B. , 2005, Blood.
[11] G. Castaldo,et al. Molecular genotyping of the Italian cohort of patients with hemophilia B. , 2005, Haematologica.
[12] M. Haase. Human recombinant factor IX: safety and efficacy studies in hemophilia B patients previously treated with plasma-derived factor IX concentrates. , 2002, Blood.
[13] J. Katz,et al. The North American Immune Tolerance Registry: Practices, Outcomes, Outcome Predictors , 2002, Thrombosis and Haemostasis.
[14] F. Rosendaal,et al. Definitions in Hemophilia , 2001, Thrombosis and Haemostasis.
[15] J. Katz. Prevalence of factor IX inhibitors among patients with haemophilia B: results of a large‐scale North American survey , 1996, Haemophilia : the official journal of the World Federation of Hemophilia.
[16] J. Goedert,et al. Loss of high‐responder inhibitors in patients with severe hemophilia A and human immunodeficiency virus type 1 infection: A report from the multi‐center hemophilia cohort study , 1993, American journal of hematology.
[17] E. Briët,et al. Inhibitors in Christmas disease. , 1984, Progress in clinical and biological research.