Alpha-1 Antitrypsin Deficiency: Principles of Care

Alpha-1 antitrypsin deficiency is an autosomal co-dominant inherited disorder that results in decreased circulating levels of alpha-1 antitrypsin (also known as alpha-1 proteinase inhibitor) and predisposes affected individuals to early onset lung and liver disease. There is currently no cure for al...

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Detalhes bibliográficos
Autor principal: Rodrigues, Joana F (author)
Outros Autores: Mineiro, Alexandra (author), Reis, António (author), Ventura, David G (author), Fernandez-Llimos, Fernando (author), Costa, Filipa (author), Gomes, Joana (author), Silva, José Manuel (author), Lopes, Paulo (author), Cordeiro, Carlos Robalo (author)
Formato: article
Idioma:eng
Publicado em: 2021
Assuntos:
Health Care Quality
Access, and Evaluation
Professional Practice
Standard of Care
alpha 1-Antitrypsin Deficiency/therapy
Texto completo:http://hdl.handle.net/10400.16/2471
País:Portugal
Oai:oai:repositorio.chporto.pt:10400.16/2471

Texto Completo

http://hdl.handle.net/10400.16/2471

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