When and how to start prophylaxis in boys with severe hemophilia without inhibitors: communication from the SSC of the ISTH
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V. Blanchette | M. Ozelo | K. Fischer | G. Young | A. Srivastava | K. Fischer | P. Collins | V. Blanchette | Peter Collins
[1] R. Ljung,et al. How to achieve full prophylaxis in young boys with severe haemophilia A: different regimens and their effect on early bleeding and venous access , 2015, Haemophilia : the official journal of the World Federation of Hemophilia.
[2] R. Ljung,et al. Bleeding before prophylaxis in severe hemophilia: paradigm shift over two decades , 2015, Haematologica.
[3] R. Ljung,et al. Definitions in hemophilia: communication from the SSC of the ISTH , 2014, Journal of thrombosis and haemostasis : JTH.
[4] R. Ljung,et al. Prospective observational cohort studies for studying rare diseases: the European PedNet Haemophilia Registry , 2014, Haemophilia : the official journal of the World Federation of Hemophilia.
[5] S. Israels,et al. Musculoskeletal health of subjects with hemophilia A treated with tailored prophylaxis: Canadian Hemophilia Primary Prophylaxis (CHPS) Study , 2013, Journal of thrombosis and haemostasis : JTH.
[6] P. Babyn,et al. Magnetic resonance imaging and joint outcomes in boys with severe hemophilia A treated with tailored primary prophylaxis in Canada , 2012, Journal of Thrombosis and Haemostasis.
[7] E. Pullenayegum,et al. Age at first joint bleed and bleeding severity in boys with severe hemophilia A: Canadian Hemophilia Primary Prophylaxis Study , 2011, Journal of thrombosis and haemostasis : JTH.
[8] L. Mantovani,et al. A randomized clinical trial of prophylaxis in children with hemophilia A (the ESPRIT Study) , 2011, Journal of thrombosis and haemostasis : JTH.
[9] M. Morfini,et al. Implications of coagulation factor VIII and IX pharmacokinetics in the prophylactic treatment of haemophilia , 2011, Haemophilia : the official journal of the World Federation of Hemophilia.
[10] A. Iorio,et al. Rate of inhibitor development in previously untreated hemophilia A patients treated with plasma‐derived or recombinant factor VIII concentrates: a systematic review , 2010, Journal of thrombosis and haemostasis : JTH.
[11] G. Auerswald,et al. New early prophylaxis regimen that avoids immunological danger signals can reduce FVIII inhibitor development , 2010, Haemophilia : the official journal of the World Federation of Hemophilia.
[12] H. Chambost,et al. Prophylaxie de longue durée chez les enfants hémophiles A et B sévères en prévention de l'arthropathie hémophilique. , 2009 .
[13] S. Jönsson,et al. Pharmacokinetics and dose requirements of factor VIII over the age range 3–74 years , 2009, European Journal of Clinical Pharmacology.
[14] C. Rothschild,et al. [French guidelines. Long-term prophylaxis for severe haemophilia A and B children to prevent haemophiliac arthropathy]. , 2009, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.
[15] 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.
[16] J. G. van der Bom,et al. Treatment-related risk factors of inhibitor development in previously untreated patients with hemophilia A: the CANAL cohort study. , 2007, Blood.
[17] P. Babyn,et al. Tailored prophylaxis in severe hemophilia A: interim results from the first 5 years of the Canadian Hemophilia Primary Prophylaxis Study , 2006, Journal of thrombosis and haemostasis : JTH.
[18] K. Fischer,et al. Can long‐term prophylaxis for severe haemophilia be stopped in adulthood? Results from Denmark and the Netherlands , 2005, British journal of haematology.
[19] D. Grobbee,et al. Factor VIII half-life and clinical phenotype of severe hemophilia A. , 2005, Haematologica.
[20] P. Petrini. How to start prophylaxis , 2003, Haemophilia : the official journal of the World Federation of Hemophilia.
[21] W. Gerbino,et al. The joint. , 2003, Acta psychologica.
[22] D. Grobbee,et al. Association between joint bleeds and Pettersson scores in severe haemophilia. , 2002, Acta radiologica.
[23] D. Grobbee,et al. The effects of postponing prophylactic treatment on long-term outcome in patients with severe hemophilia. , 2002, Blood.
[24] A. Miners,et al. Experience of prophylaxis treatment in children with severe haemophilia , 2002, Haemophilia : the official journal of the World Federation of Hemophilia.
[25] F. Beek,et al. Long‐term outcome of individualized prophylactic treatment of children with severe haemophilia , 2001, British journal of haematology.
[26] A. Shapiro,et al. Pharmacokinetics of recombinant factor IX in relation to age of the patient: implications for dosing in prophylaxis , 2001, Haemophilia : the official journal of the World Federation of Hemophilia.
[27] Gilbert. Musculoskeletal complications of haemophilia: the joint , 2000, Haemophilia : the official journal of the World Federation of Hemophilia.
[28] J. Astermark,et al. Primary prophylaxis in severe haemophilia should be started at an early age but can be individualized , 1999, British journal of haematology.
[29] C. Kessler,et al. When should prophylactic treatment in patients with haemophilia A and B start?— The German experience , 1998, Haemophilia : the official journal of the World Federation of Hemophilia.
[30] K. Khair,et al. The impact of prophylactic treatment on children with severe haemophilia , 1996, British journal of haematology.
[31] H. Pettersson. Radiographic scores and implications. , 1993, Seminars in hematology.
[32] H. Pettersson,et al. Twenty‐five years' experience of prophylactic treatment in severe haemophilia A and B , 1992, Journal of internal medicine.
[33] Å. Ahlberg,et al. HAEMOPHILIA PROPHYLAXIS IN SWEDEN , 1976, Acta paediatrica Scandinavica.