Musculoskeletal problems in persons with inhibitors: How do we treat?
Author:
Publisher
Wiley
Subject
Genetics (clinical),Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2516.2012.02874.x/fullpdf
Reference40 articles.
1. Inhibitors: resolving diagnostic and therapeutic dilemmas;Dimichele;Haemophilia,2002
2. Careri D Personal Communication 2007
3. The incidence of factor VIII and factor IX inhibitors in the hemophilia population of the UK and their effect on subsequent mortality, 1977-99;Darby;J Thromb Haemost,2004
4. Comparitive thrombotic event incidence after infusion of recombinant factor VIIa versus factor VIII inhibitor bypass activity;Aledort;J Thromb Haemost,2004
5. Safety update on the use of recombinant activated factor VII and the treatment of congenital and acquired deficiency of factor VIII or IX and inhibitors;Abshire;Haemophilia,2008
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1. 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
2. Recommendations on multidisciplinary management of elective surgery in people with haemophilia;Haemophilia;2018-06-26
3. Manual therapy in the treatment of patients with hemophilia B and inhibitor;BMC Musculoskeletal Disorders;2018-01-22
4. Comprehensive care of the patient with haemophilia and inhibitors undergoing surgery: practical aspects;Haemophilia;2012-08-27
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