Hereditary angioedema with C1 inhibitor deficiency: delay in diagnosis in Europe

BACKGROUND: Hereditary angioedema (HAE) is a rare, debilitating, and potentially life-threatening disease characterized by recurrent edema attacks. Important advances in HAE treatment have been made, including the development of new therapies for treating or preventing attacks. Nevertheless, the dis...

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Detalles Bibliográficos
Autores principales: Zanichelli, Andrea, Magerl, Markus, Longhurst, Hilary, Fabien, Vincent, Maurer, Marcus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3751114/
https://www.ncbi.nlm.nih.gov/pubmed/23937903
http://dx.doi.org/10.1186/1710-1492-9-29

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3751114/
https://www.ncbi.nlm.nih.gov/pubmed/23937903
http://dx.doi.org/10.1186/1710-1492-9-29

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