Pathophysiology of inhibitors to factor VIII in patients with haemophilia A
Author:
Publisher
Wiley
Subject
Genetics(clinical),Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2516.2002.00624.x/fullpdf
Reference57 articles.
1. A more uniform measurement of factor VIII inhibitors;Kasper;Thromb Diath Haemorrh,1975
2. An introduction to FVIII inhibitors: the detection and quantitation;Kessler;Am J Med,1991
3. The Nijmegen modification of the Bethesda assay for Factor VIII:C inhibitors: improved specificity and reliability;Verbruggen;Thromb Haemost,1995
4. Haemophilia A: mutation type determines risk of inhibitor formation;Schwaab;Thromb Haemost,1995
5. Natural antibodies to factor VIII (anti-hemophilic factor) in healthy individuals;Algiman;Proc Natl Acad Sci USA,1992
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1. Comparative glycosylation mapping of plasma-derived and recombinant human factor VIII;PLOS ONE;2020-05-22
2. Population-specific design of de-immunized protein biotherapeutics;PLOS Computational Biology;2018-03-02
3. Joint bleeds increase the inhibitor response to human factor VIII in a rat model of severe haemophilia A;Haemophilia;2016-07-21
4. Antibody response to recombinant human coagulation factor VIII in a new rat model of severe hemophilia A;Journal of Thrombosis and Haemostasis;2016-03-08
5. Therapeutic outcomes, assessments, risk factors and mitigation efforts of immunogenicity of therapeutic protein products;Cellular Immunology;2015-06
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