Prevalent inhibitors in haemophilia B subjects enrolled in the Universal Data Collection database-Reference-Cited by-同舟云学术

Prevalent inhibitors in haemophilia B subjects enrolled in the Universal Data Collection database

Published:2013-07-16 Issue:1 Volume:20 Page:25-31
ISSN:1351-8216
Container-title:Haemophilia
language:en
Short-container-title:Haemophilia

Author:

Puetz J.¹,Soucie J. M.²,Kempton C. L.³,Monahan P. E.⁴⁵,

Affiliation:

1. Division of Hematology/Oncology; Department of Pediatrics; Saint Louis University; St. Louis MO USA

2. Division of Blood Disorders; National Center for Birth Defects and Developmental Disabilities; Centers for Disease Control and Prevention; Atlanta GA USA

3. Departments of Pediatrics and Hematology/Oncology; Emory University; Atlanta GA USA

4. Department of Pediatrics; University of North Carolina at Chapel Hill; Chapel Hill NC USA

5. Division of Blood Disorders; National Center for Birth Defects and Developmental Disabilities; Atlanta GA USA

Publisher

Wiley

Subject

Genetics(clinical),Hematology,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/hae.12229/fullpdf

Reference19 articles.

1. Risk stratification for inhibitor development at first treatment for severe hemophilia A: a tool for clinical practice;Avest;J Thromb Haemost,2008

2. Inhibitors in factor IX deficiency a report of the ISTH-SSC international FIX inhibitor registry (1997-2006);Chitlur;Haemophilia,2009

3. The North American Immune Tolerance Registry: practices, outcomes, outcome predictors;DiMichele;Thromb Haemost,2002

4. Inhibitor development in haemophilia B: an orphan disease in need of attention;DiMichele;Br J Haematol,2007

5. Inhibitors in Christmas disease;Briet;Prog Clin Biol Res,1984

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