Clinical trials and registries in haemophilia: Opponents or collaborators? Comparison of PUP data derived from different data sources
Author:
Affiliation:
1. Hematology and Transfusion Medicine; Paul-Ehrlich-Institut; Langen Germany
2. Medicine Evaluation Board; Utrecht The Netherlands
3. PedNet Haemophilia Research Foundation; Baarn The Netherlands
Publisher
Wiley
Subject
Genetics(clinical),Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/hae.13421/fullpdf
Reference38 articles.
1. Factor VIII safety: plasma-derived versus recombinant products;Gringeri;Blood Transfus,2011
2. Emerging and future therapies for haemophilia;Carr;J Blood Med,2015
3. FVIII inhibitors: pathogenesis and avoidance;Astermark;Blood,2015
4. How we treat a haemophilia A patient with a factor VIII inhibitor;Kempton;Blood,2009
5. Articular status of haemophilia patients with inhibitors;Morfini;Haemophilia,2008
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3. Epidemiological Challenges in Rare Bleeding Disorders: FVIII Inhibitor Incidence in Haemophilia A Patients—A Known Issue of Unknown Origin;International Journal of Environmental Research and Public Health;2020-12-30
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5. Kreuth V initiative: European consensus proposals for treatment of hemophilia using standard products, extended half-life coagulation factor concentrates and non-replacement therapies;Haematologica;2020-05-28
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