International collaboration is needed to reduce the risk for inhibitors in PUPs with severe haemophilia A
Author:
Affiliation:
1. World Federation of Hemophilia; Montréal QC Canada
Publisher
Wiley
Subject
Genetics(clinical),Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/hae.13512/fullpdf
Reference11 articles.
1. Use of recombinant antihemophilic factor in the treatment of two patients with classic hemophilia;White;N Engl J Med,1989
2. A sudden increase in factor VIII inhibitor development in multitransfused hemophilia A patients in The Netherlands. Dutch Hemophilia Study Group;Rosendaal;Blood,1993
3. Factor VIII inhibitors in previously treated haemophilia A patients with a double virus-inactivated plasma derived factor VIII concentrate;Peerlinck;Thromb Haemost,1997
4. Increased inhibitor incidence in severe haemophilia A since 1990 attributable to more low titre inhibitors;Berg;Thromb Haemost,2016
5. Rate of inhibitor development in previously untreated hemophilia A patients treated with plasma-derived or recombinant factor VIII concentrates: a systematic review;Iorio;J Thromb Haemost,2010
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1. How I approach: Previously untreated patients with severe congenital hemophilia A;Pediatric Blood & Cancer;2018-09-24
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