Inhibitors in haemophilia: clinical aspects
暂无分享,去创建一个
[1] Mary E. Martin. Management of the , 2005 .
[2] S. Darby,et al. The incidence of factor VIII and factor IX inhibitors in the hemophilia population of the UK and their effect on subsequent mortality, 1977–99 , 2004, Journal of thrombosis and haemostasis : JTH.
[3] P. Mannucci. Hemophilia: treatment options in the twenty‐first century , 2003, Journal of thrombosis and haemostasis : JTH.
[4] D. DiMichele. Immune tolerance therapy dose as an outcome predictor , 2003, Haemophilia : the official journal of the World Federation of Hemophilia.
[5] V. Blanchette,et al. Intensive exposure to factor VIII is a risk factor for inhibitor development in mild hemophilia A , 2003, Journal of thrombosis and haemostasis : JTH.
[6] A. Mäkipernaa,et al. Long‐term FEIBA prophylaxis does not prevent progression of existing joint disease , 2003, Haemophilia : the official journal of the World Federation of Hemophilia.
[7] K. Fischer,et al. Age at first treatment and immune tolerance to factor VIII in severe hemophilia , 2003, Thrombosis and Haemostasis.
[8] S. M. Carvalho,et al. Hemophilia care in the state of Rio de Janeiro, Brazil. , 2003, Revista panamericana de salud publica = Pan American journal of public health.
[9] G. Auerswald,et al. Epidemiology of inhibitors and current treatment strategies. , 2003, Haematologica.
[10] R. Ljung,et al. Breastfeeding does not influence the development of inhibitors in haemophilia , 2002, Haemophilia : the official journal of the World Federation of Hemophilia.
[11] R. Ljung,et al. Inhibitors in the Swedish population with severe haemophilia A and B: a 20‐year survey , 2002, Acta paediatrica.
[12] S. Antunes. Haemophilia in the developing world: the Brazilian experience , 2002, Haemophilia : the official journal of the World Federation of Hemophilia.
[13] J. Katz,et al. The North American Immune Tolerance Registry: Practices, Outcomes, Outcome Predictors , 2002, Thrombosis and Haemostasis.
[14] C. Altisent,et al. Incidence of factor VIII inhibitors in severe haemophilia: the importance of patient age , 2001, British journal of haematology.
[15] J. Astermark,et al. The Malmö International Brother Study (MIBS): further support for genetic predisposition to inhibitor development , 2001, Haemophilia : the official journal of the World Federation of Hemophilia.
[16] Lee,et al. Oral immune tolerance induction to factor VIII via breast milk, a possibility? , 2000, Haemophilia : the official journal of the World Federation of Hemophilia.
[17] J. Oldenburg,et al. NovoSeven® in immune tolerance therapy , 2000, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.
[18] B. Kroner. Comparison of the International Immune Tolerance Registry and the North American Immune Tolerance Registry , 1999, Vox Sanguinis.
[19] C. Rothschild,et al. Multicenter comparison of inhibitor (Inh) development on plasma-derived (PD) vs recombinant (rec) factor VIII(fVIII) in severe hemophilia a patients (sHA pts) , 1998 .
[20] M. Chandy,et al. Management of haemophilia in the developing world , 1998, Haemophilia : the official journal of the World Federation of Hemophilia.
[21] C. Kessler,et al. Management of haemophilia B patients with inhibitors and anaphylaxis , 1998, Haemophilia : the official journal of the World Federation of Hemophilia.
[22] J. Oldenburg,et al. Immune Tolerance for the Treatment of Factor VIII Inhibitors ‐ Twenty Years' ‘Bonn Protocol’ , 1996, Vox sanguinis.
[23] H. M. van den Berg,et al. Low-dose immune tolerance induction in hemophilia A patients with inhibitors. , 1995, Blood.
[24] G. Mariani,et al. Immune Tolerance in Hemophilia-Principal Results from the International Registry , 1994, Thrombosis and Haemostasis.
[25] F. Gill. The natural history of factor VIII inhibitors in patients with hemophilia A. , 1984, Progress in clinical and biological research.
[26] Emrys D. Jones. The Developing World , 1963, Nature.