Inhibitors in the Swedish population with severe haemophilia A and B: a 20-year survey
Author:
Publisher
Wiley
Subject
General Medicine,Pediatrics, Perinatology and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1651-2227.2002.tb02854.x/fullpdf
Reference28 articles.
1. Incidence of development of factor VIII and factor IX inhibitors in haemophiliacs [see comments];Ehrenforth;Lancet,1992
2. Frequency of inhibitor development in haemophiliacs treated with low-purity factor VIII [see comments];Addiego;Lancet,1993
3. Recombinant factor VIII for the treatment of previously untreated patients with hemophilia A. Safety, efficacy, and development of inhibitors. Kogenate Previously Untreated Patient Study Group;Lusher;N Engl J Med,1993
4. A multicenter study of recombinant factor VIII (recombinate): safety, efficacy, and inhibitor risk in previously untreated patients with hemophilia A. The Recombinate Study Group;Bray;Blood,1994
5. Prevalence of inhibitors in a population of 3435 hemophilia patients in France. French Hemophilia Study Group;Sultan;Thromb Haemost,1992
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