Monitoring joint health in haemophilia: Factors associated with deterioration

Author:

Kuijlaars I. A. R.12ORCID,Timmer M. A.123ORCID,de Kleijn P.13,Pisters M. F.234,Fischer K.1ORCID

Affiliation:

1. Van Creveldkliniek; University Medical Center Utrecht; Utrecht The Netherlands

2. Physical Therapy Sciences; Program in Clinical Health Sciences; University Medical Center Utrecht; Utrecht The Netherlands

3. Physical Therapy Research; Department of Rehabilitation, Physiotherapy Science & Sport; Brain Center Rudolf Magnus; University Medical Center Utrecht; Utrecht The Netherlands

4. Center for Physical Therapy Research and Innovation in Primary Care; Leidsche Rijn Julius Health Care Centers; Utrecht The Netherlands

Publisher

Wiley

Subject

Genetics(clinical),Hematology,General Medicine

Reference27 articles.

1. Guidelines for the management of hemophilia;Srivastava;Haemophilia,2013

2. Understanding haemophilic arthropathy: an exploration of current open issues;Jansen;Br J Haematol,2008

3. Clotting factor concentrates given to prevent bleeding and bleeding-related complications in people with hemophilia A or B;Iorio;Cochrane Database Syst Rev,2011

4. Prophylaxis of joint hemorrhages in hemophilia;Creveld;Acta Haematol,1971

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