Ecallantide for the Treatment of Hereditary Angiodema in Adults

Hereditary angioedema (HAE) is a clinical disorder characterized by a deficiency of C1 esterase inhibitor (C1-INH). HAE has traditionally been divided into two subtypes. Unique among the inherited deficiencies of the complement system, HAE Types I and II are inherited as an autosomal dominant disord...

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Detalles Bibliográficos
Autores principales: Lunn, Michael, Banta, Erin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Libertas Academica 2011
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3115639/
https://www.ncbi.nlm.nih.gov/pubmed/21695090
http://dx.doi.org/10.4137/CMC.S4434

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3115639/
https://www.ncbi.nlm.nih.gov/pubmed/21695090
http://dx.doi.org/10.4137/CMC.S4434

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