Inhibitors: our greatest challenge. Can we minimize the incidence?
Author:
Affiliation:
1. School of Medicine Section of Hematology/Oncology; Tulane University; New Orleans; LA; USA
Publisher
Wiley
Subject
Genetics(clinical),Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/hae.12049/fullpdf
Reference17 articles.
1. The changing prognosis of classic hemophilia (factor VIII “deficiency”);Jones;Ann Intern Med,1991
2. Incidence of factor VIII inhibitors in severe haemophilia: the importance of patient age;Lorenzo;Br J Haematol,2001
3. Age at first treatment and immune tolerance to factor VIII in severe hemophilia;van der Bom;Thromb Haemost,2003
4. Early factor VIII exposure and subsequent inhibitor development in children with severe haemophilia A;Chalmers;Haemophilia,2007
5. Environmental risk factors for inhibitor development in children with haemophilia A: a case-control study;Santagostino;Br J Haematol,2005
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