Methodologies for data collection in congenital haemophilia with inhibitors (CHwI): critical assessment of the literature and lessons learned from recombinant factor VIIa
Author:
Affiliation:
1. Georgetown University Medical Center; Washington DC USA
2. Novo Nordisk Health Care AG; Zurich Switzerland
3. Division of Emergency Medicine; McMaster University; Hamilton ON Canada
Funder
Bayer
Shire
Novo Nordisk
Genentech
Octopharma
Publisher
Wiley
Subject
Genetics(clinical),Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/hae.13482/fullpdf
Reference48 articles.
1. Factor VIII gene (F8) mutation and risk of inhibitor development in nonsevere hemophilia A;Eckhardt;Blood,2013
2. The epidemiology of inhibitors in haemophilia A: a systematic review;Wight;Haemophilia,2003
3. Inhibitor development in haemophilia B: an orphan disease in need of attention;DiMichele;Br J Haematol,2007
4. Treatment and prevention of bleeds in haemophilia patients with inhibitors to factor VIII/IX;Rocino;J Clin Med,2017
5. Guidelines for the management of hemophilia;Srivastava;Haemophilia,2013
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