Angioedema and the Canadian Network of Rare Blood Disorder Organizations: extending the Canadian hemophilia care model.
作者： T. Bowen
DOI: 10.1503/CMAJ.061236
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摘要: In response to a push by Canadian patients with hereditary angioedema (HAE) who have recognized that the diagnosis and management of HAE was lagging behind many European countries (such as Italy, Hungary Germany),[1][1],[2][2] Jeanne Burnham colleagues organized
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