Immunogenicity of factor VIII concentrates in patients with hemophilia: a randomized clinical trial is warranted
Author:
Publisher
American Society of Hematology
Subject
Cell Biology,Hematology,Immunology,Biochemistry
Link
http://ashpublications.org/blood/article-pdf/110/8/3084/1296582/zh802007003084.pdf
Reference5 articles.
1. Recombinant versus plasma-derived factor VIII products and the development of inhibitors in previously untreated patients with severe hemophilia A: the CANAL cohort study.;Gouw;Blood,2007
2. The epidemiology of inhibitors in haemophilia A: a systematic review.;Wight;Haemophilia,2003
3. Influence of the type of factor VIII concentrate on the incidence of factor VIII inhibitors in previously untreated patients with severe hemophilia A.;Goudemand;Blood,2006
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
Cited by 6 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Risk factors for inhibitor development in severe hemophilia A;Thrombosis Research;2018-08
2. To serve and protect: The modulatory role of von Willebrand factor on factor VIII immunogenicity;Blood Reviews;2017-09
3. Inhibitor development after switching of FVIII concentrate in multitransfused patients with severe haemophilia A;Haemophilia;2014-04-03
4. Kinetics of the interaction between anti-FVIII antibodies and FVIII from therapeutic concentrates, with and without von Willebrand factor, assessed by surface plasmon resonance;Haemophilia;2012-05-30
5. Therapeutic properties and safety of recombinant factor VIII and factor IX;Polish Archives of Internal Medicine;2009-06-01
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