Improving the Lives of Patients with Alpha-1 Antitrypsin Deficiency

Alpha-1 Antitrypsin Deficiency (AATD) is a rare genetic condition that predisposes patients to lung and liver disease and is often underdiagnosed due to incomplete diagnosis of chronic obstructive pulmonary disease (COPD) and asthma. Improvements in physician awareness have been made, but better str...

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Detalles Bibliográficos
Autores principales: Sandhaus, Robert A, Strange, Charlie, Zanichelli, Andrea, Skålvoll, Karen, Koczulla, Andreas Rembert, Stockley, Robert A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2020
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7735792/
https://www.ncbi.nlm.nih.gov/pubmed/33328731
http://dx.doi.org/10.2147/COPD.S276773

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7735792/
https://www.ncbi.nlm.nih.gov/pubmed/33328731
http://dx.doi.org/10.2147/COPD.S276773

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