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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2017
Materias:
3900
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5313030/
https://www.ncbi.nlm.nih.gov/pubmed/28178173
http://dx.doi.org/10.1097/MD.0000000000006109

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5313030/
https://www.ncbi.nlm.nih.gov/pubmed/28178173
http://dx.doi.org/10.1097/MD.0000000000006109

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