Optimizing the treatment of haemophilia B: laboratory and clinical perspectives
Author:
Publisher
Wiley
Subject
Genetics(clinical),Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2516.2010.02298.x/fullpdf
Reference11 articles.
1. Srivastava A Giangrande P Poon MC Chua , M McCraw A Wiedel J Guidelines for the Management of Hemophilia http://www.wfh.org/index.asp?lang=EN
2. Recombinant factor IX;White;Thromb Haemost,1997
3. Pharmacokinetic analysis of plasma-derived and recombinant F IX concentrates in previously treated patients with moderate or severe hemophilia B;Ewenstein;Transfusion,2002
4. Pharmacokinetics of factors IX, recombinant activated factor VII and factor XIII;Poon;Haemophilia,2006
5. In vivo recovery of factor VIII and factor IX: intra- and interindividual variance in a clinical setting;Bjorkman;Haemophilia,2007
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1. A novel missense mutation in F9 gene causes hemophilia B in a family with clinical variability;Blood Coagulation & Fibrinolysis;2020-03
2. Treatment trends for haemophilia A and haemophilia B in the United States: results from the 2010 practice patterns survey;Haemophilia;2012-03-12
3. Haemophilia B: impact on patients and economic burden of disease;Thrombosis and Haemostasis;2011
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