Portuguese consensus document for the management of alpha-1-antitrypsin deficiency

Alpha-1-antitrypsin deficiency (AATD) is a genetic autosomal codominant disorder caused by mutations in SERPINA1 gene. It is one of the most prevalent genetic disorders, although it remains underdiagnosed. Whereas at international level there are several areas of consensus on this disorder, in Portu...

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Detalhes bibliográficos
Autor principal: Lopes, A. (author)
Outros Autores: Mineiro, M. (author), Costa, F. (author), Gomes, J. (author), Santos, C. (author), Antunes, C. (author), Maia, D. (author), Melo, R. (author), Canotilho, M. (author), Magalhães, E. (author), Vicente, I. (author), Valente, C. (author), Gonçalves, B. (author), Conde, B. (author), Guimarães, C. (author), Sousa, C. (author), Amado, J. (author), Brandão, M. (author), Sucena, M. (author), Oliveira, M. (author), Seixas, S. (author), Teixeira, V. (author), Telo, L. (author)
Formato: article
Idioma:eng
Publicado em: 2020
Assuntos:
Consensus
Diagnosis
Pulmonary Emphysema
Therapeutics
alpha 1-Antitrypsin Deficiency
Texto completo:http://hdl.handle.net/10400.16/2320
País:Portugal
Oai:oai:repositorio.chporto.pt:10400.16/2320

Texto Completo

http://hdl.handle.net/10400.16/2320

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