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, J (author)
Outros Autores: Mineiro, A (author), Reis, A (author), Ventura, D (author), Fernandez-Llimos, F (author), Costa, F (author), Gomes, J (author), Silva, JM (author), Lopes, P (author), Robalo Cordeiro, C (author)
Formato: article
Idioma:eng
Publicado em: 2020
Assuntos:
HSM PNEU
Health Care Quality, Access, and Evaluation
Professional Practice
Standard of Care
alpha 1-Antitrypsin Deficiency/therapy
Texto completo:http://hdl.handle.net/10400.17/3478
País:Portugal
Oai:oai:repositorio.chlc.min-saude.pt:10400.17/3478

Texto Completo

http://hdl.handle.net/10400.17/3478

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