Screening for hereditary angioedema (HAE) at 13 emergency centers in Osaka, Japan: A prospective observational study

Hereditary angioedema (HAE) with deficiency of C1 inhibitor (C1-INH) is an autosomal-dominant disease characterized by recurrent episodes of potentially life-threatening angioedema. The objective is to study the incidence of HAE among patients who visit the emergency department. This was a 3-year pr...

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Detalhes bibliográficos
Publicado no:Medicine (Baltimore)
Main Authors: Hirose, Tomoya, Kimbara, Futoshi, Shinozaki, Masahiro, Mizushima, Yasuaki, Yamamoto, Hidehiko, Kishi, Masashi, Kiguchi, Takeyuki, Shiono, Shigeru, Noborio, Mitsuhiro, Fuke, Akihiro, Akimoto, Hiroshi, Kimura, Takaaki, Kaga, Shinichiro, Horiuchi, Takahiko, Shimazu, Takeshi
Formato: Artigo
Idioma:Inglês
Publicado em: Wolters Kluwer Health 2017
Assuntos:
3900
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5313030/
https://ncbi.nlm.nih.gov/pubmed/28178173
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MD.0000000000006109
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