Patterns of tertiary prophylaxis in Canadian adults with severe and moderately severe haemophilia B

Author:

Jackson S. C.1,Yang M.2,Minuk L.3,St-Louis J.4,Sholzberg M.5,Card R.6,Iorio A.7,Poon M.-C.8

Affiliation:

1. Division of Hematology; Department of Medicine; University of British Columbia; Vancouver BC Canada

2. British Columbia Provincial Bleeding Disorders Program - Adult Division; Vancouver BC Canada

3. Schulich School of Medicine and Dentistry; University of Western Ontario; London ON Canada

4. CHU-Sainte-Justine and Department of Medicine; University of Montreal; Montreal QC Canada

5. St Michael's Hospital; Toronto ON Canada

6. Division of Hematology; Department of Medicine; University of Saskatchewan; Saskatoon SK Canada

7. Clinical Epidemiology & Biostatistics and Medicine; McMaster University; Hamilton ON Canada

8. Division of Hematology and Hematologic Malignancies; Department of Medicine; University of Calgary; Calgary AB Canada

Publisher

Wiley

Subject

Genetics(clinical),Hematology,General Medicine

Reference22 articles.

1. Christmas Disease: a condition previously mistaken for haemophilia;Biggs;Br Med J,1952

2. On the epidemiology of hemophilia and Christmas Disease;Ratnoff;N Engl J Med,1957

3. Evaluation of prophylactic replacement therapy in haemophilia B;Morfini;Scand J Haematol,1976

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

5. Prophylactic factor replacement in hemophilia;Carcao;Blood Rev,2004

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