Diagnosis and treatment of factor VIII and IX inhibitors in congenital haemophilia: (4th edition)-Reference-Cited by-同舟云学术

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Diagnosis and treatment of factor VIII and IX inhibitors in congenital haemophilia: (4th edition)

Published:2012-11-15 Issue:2 Volume:160 Page:153-170
ISSN:0007-1048
Container-title:British Journal of Haematology
language:en
Short-container-title:Br J Haematol

Author:

Collins Peter W.¹,Chalmers Elizabeth²,Hart Daniel P.³,Liesner Ri⁴,Rangarajan Savita⁵,Talks Kate⁶,Williams Mike⁷,Hay Charles R.⁸

Affiliation:

1. School of Medicine; Cardiff University; University Hospital of Wales; Wales; UK

2. Royal Hospital for Sick Children; Glasgow; UK

3. The London School of Medicine and Dentistry; Royal London Hospital; Barts, Queen Mary University; London; UK

4. Great Ormond Street NHS Trust; London; UK

5. Hampshire Hospital NHS Foundation Trust; Basingstoke & North Hampshire Hospital; Basingstoke; UK

6. Royal Victoria Infirmary; Newcastle upon Tyne; UK

7. Birmingham Childrens' Hospital NHS Foundation Trust; Birmingham; UK

8. Central Manchester University Hospitals; Manchester; UK

Publisher

Wiley

Subject

Hematology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/bjh.12091/fullpdf

Reference132 articles.

1. Comparative thrombotic event incidence after infusion of recombinant factor VIIa versus factor VIII inhibitor bypass activity;Aledort;Journal of Thrombosis and Haemostasis,2004

2. Can B-domain deletion alter the immunogenicity of recombinant factor VIII? A meta-analysis of prospective clinical studies;Aledort;Journal of Thrombosis and Haemostasis,2011a

3. Best evidence on B-domain deletion and the immunogenicity of recombinant factor VIII;Aledort;Journal of Thrombosis and Haemostasis,2011b

4. Rituximab and desensitization for a patient with severe factor IX deficiency, inhibitors, and history of anaphylaxis;Alexander;Journal of Pediatric Hematology/oncology,2008

5. The Malmö International Brother Study (MIBS): further support for genetic predisposition to inhibitor development in hemophilia patients;Astermark;Haemophilia,2001

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