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Comment
. 2006 Oct 24;175(9):1083.
doi: 10.1503/cmaj.061236.

Angioedema and the Canadian Network of Rare Blood Disorder Organizations: extending the Canadian hemophilia care model

Tom Bowen  1
Affiliations
Comment

Angioedema and the Canadian Network of Rare Blood Disorder Organizations: extending the Canadian hemophilia care model

Tom Bowen. CMAJ. .
No abstract available

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References

    1. Bowen T (guest editor). Editorial. Transfus Apher Sci 2003;29:193-4.
    1. Agostoni A, Aygoren-Pursun E, Binkley KE, et al. Hereditary and acquired angioedema: problems and progress. Proceedings of the third C1 Esterase Inhibitor Deficiency Workshop and beyond. J Allergy Clin Immunol 2004;114:S51-131. - PMC - PubMed
    1. Bowen T, Hebert J, Ritchie B, et al. Management of hereditary angioedema: a Canadian approach. Transfus Apher Sci 2003;29:205-14. - PubMed
    1. Bowen T, Cicardi M, Farkas H, et al. Canadian 2003 international consensus algorithm for the diagnosis, therapy, and management of hereditary angioedema. J Allergy Clin Immunol 2004;114:629-37. - PubMed
    1. Page D. Network of Rare Blood Disorder Organizations: evaluation report. 2006. Available: www.hemophilia.ca/nrbdo/en/objectives.php (accessed 2006 Sept 25).