The prevalence and risk factors of inhibitor development of FVIII in previously treated patients with hemophilia A
Author:
Affiliation:
1. Department of Pediatrics, Eulji University School of Medicine, Daejeon, Korea
Publisher
The Korean Society of Hematology
Subject
Hematology
Link
https://synapse.koreamed.org/pdf/10.5045/br.2019.54.3.204
Reference19 articles.
1. Genetic risk factors for inhibitors to factors VIII and IX
2. Inhibitors to Factor VIII: Immunology
3. Recombinant Factor VIII for the Treatment of Previously Untreated Patients with Hemophilia A -- Safety, Efficacy, and Development of Inhibitors
4. French Previously Untreated Patients with Severe Hemophilia A after Exposure to Recombinant Factor VIII : Incidence of Inhibitor and Evaluation of Immune Tolerance
5. Absence of Inhibitors in Previously Untreated Patients with Severe Haemophilia A after Exposure to a Single Intermediate Purity Factor VIII Product
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1. Report on the diagnosis and treatment of hemophilia in China (Version 2024);LabMed Discovery;2024-07
2. Incidence and treatment-related risk factors of inhibitor development after intensive FVIII replacement for major orthopaedic surgery in previous treated haemophilia A;Journal of Orthopaedic Surgery and Research;2024-06-16
3. Comprehensive domain-specific analysis and immunoglobulin G profiling of anti–factor VIII antibodies using a bead-based multiplex immunoassay;Journal of Thrombosis and Haemostasis;2024-06
4. Challenges in prophylactic therapy with Emicizumab in patients with hemophilia A: Focus on monitoring tests;Revista Romana de Medicina de Laborator;2024-01-01
5. Association between interleukin-2 (rs2069762) gene polymorphism and FVIII inhibitor development in Indonesian patients with severe hemophilia A;Medical Journal of Indonesia;2023-03-08
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