Determinants of airflow obstruction in severe alpha‐1‐antitrypsin deficiency

BACKGROUND: Severe α(1)‐antitrypsin (AAT) deficiency is an autosomal recessive genetic condition associated with an increased but variable risk for chronic obstructive pulmonary disease (COPD). A study was undertaken to assess the impact of chronic bronchitis, pneumonia, asthma and sex on the develo...

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Detalhes bibliográficos
Main Authors: DeMeo, Dawn L, Sandhaus, Robert A, Barker, Alan F, Brantly, Mark L, Eden, Edward, McElvaney, N Gerard, Rennard, Stephen, Burchard, Esteban, Stocks, James M, Stoller, James K, Strange, Charlie, Turino, Gerard M, Campbell, Edward J, Silverman, Edwin K
Formato: Artigo
Idioma:Inglês
Publicado em: BMJ Group 2007
Assuntos:
Alpha-1-Antitrypsin Deficiency
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2117297/
https://ncbi.nlm.nih.gov/pubmed/17389752
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/thx.2006.075846
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