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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Bibliographic Details
Main Author: Lopes, A. (author)
Other Authors: 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)
Format: article
Language:eng
Published: 2020
Subjects:
Consensus
Diagnosis
Pulmonary Emphysema
Therapeutics
alpha 1-Antitrypsin Deficiency
Online Access:http://hdl.handle.net/10400.16/2320
Country:Portugal
Oai:oai:repositorio.chporto.pt:10400.16/2320

Internet

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

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