Primary prophylaxis in severe haemophilia should be started at an early age but can be individualized

Author:

Astermark Jan,Petrini Pia,Tengborn Lilian,Schulman Sam,Ljung Rolf,Berntorp Erik

Publisher

Wiley

Subject

Hematology

Reference18 articles.

1. Haemophilia in Sweden. VII. Incidence, treatment and prophylaxis of arthropathy and other musculoskeletal manifestations of haemophilia A and B;Ahlberg;Acta Orthopaedica Scandinavica,1965

2. A longitudinal study of orthopaedic outcomes for severe factor VIII-deficient haemophiliacs. The Orthopaedic Outcome Study Group;Aledort;Journal of Internal Medicine,1994

3. Methods of hemophilia care delivery; regular prophylaxis vs. episodic treatment;Berntorp;Haemophilia,1995

4. Variation in factor VIII inhibitor reactivity with different commercial factor VIII preparations;Berntorp;Haemophilia,1996

5. Central venous access devices in children with hemophilia: an up-date;Blanchette;Blood Coagulation and Fibrinolysis,1997

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