Inhibitors in haemophilia A: a perspective on clotting factor products as a potential contributing factor
Author:
Affiliation:
1. Bayer HealthCare Pharmaceuticals Inc. Whippany NJ USA
2. Bayer Pharma AG Leverkusen Germany
3. Michigan State University East Lansing MI USA
Funder
Bayer HealthCare
Publisher
Wiley
Subject
Genetics(clinical),Hematology,General Medicine
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/hae.12888
Reference56 articles.
1. Overview of Inhibitors
2. Why do inhibitors develop? Principles of and factors influencing the risk for inhibitor development in haemophilia
3. Inhibitor development: patient-determined risk factors
4. Incidence of development of factor VIII and factor IX inhibitors in haemophiliacs
5. Recombinant factor VIII products and inhibitor development in previously untreated boys with severe hemophilia A
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1. Hemophilia A and Hemophilia B;Consultative Hemostasis and Thrombosis;2019
2. The inhibitors – a challenge for the management of patients with hereditary haemophilia A;Romanian Journal of Internal Medicine;2018-08-29
3. Safety and Efficacy of B-domain Deleted Third Generation Recombinant Factor VIII (GreenGene F™) in Korean Patients with Hemophilia A: Data from a Post-marketing Surveillance Study;Journal of Korean Medical Science;2018
4. Analyses of the FranceCoag cohort support differences in immunogenicity among one plasma-derived and two recombinant factor VIII brands in boys with severe hemophilia A;Haematologica;2017-10-12
5. Baby hamster kidney cell–derived recombinant factor VIII: a quarter century of learning and clinical experience;Expert Review of Hematology;2016-11-28
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