Optimal treatment regimens for patients with bleeding disorders
Author:
Publisher
Wiley
Subject
Genetics(clinical),Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2516.2001.00525.x/fullpdf
Reference33 articles.
1. Åhlberg A Haemophilia in Sweden. VII. Incidence, treatment and prophylaxis of arthropathy and other musculoskeletal manifestations of haemophilia A and B Acta Orthopaedica Scand 1965 77
2. Twenty-five years’ experience of prophylactic treatment in severe haemophilia A and B;Nilsson;J Int Med,1992
3. A longitudinal study of orthopaedic outcomes for severe factor VIII-deficient haemophiliacs;Aledort;J Int Med,1994
4. Treatment of children with haemophilia in Europe: a survey of 20 centres in 16 countries;Ljung;Haemophilia,2000
5. The impact of prophylactic treatment on children with severe haemophilia;Leisner;Br J Haematol,1996
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