The Global Registry for Hereditary Angioedema due to C1-Inhibitor Deficiency

Hereditary angioedema (HAE) is a rare condition, mostly due to genetic deficiency of complement C1 inhibitor (C1-INH). The rarity of HAE impedes extensive data collection and assessment of the impact of certain factors known to affect the course of this disabling and life-threatening disease. Establ...

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Detalles Bibliográficos
Autores principales: Zanichelli, Andrea, Farkas, Henriette, Bouillet, Laurance, Bara, Noemi, Germenis, Anastasios E., Psarros, Fotis, Varga, Lilian, Andrási, Noemi, Boccon-Gibod, Isabelle, Castiglioni Roffia, Marco, Rutkowski, Michal, Cancian, Mauro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8282542/
https://www.ncbi.nlm.nih.gov/pubmed/33791951
http://dx.doi.org/10.1007/s12016-021-08855-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8282542/
https://www.ncbi.nlm.nih.gov/pubmed/33791951
http://dx.doi.org/10.1007/s12016-021-08855-4

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