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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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| Publicat a: | Int J Chron Obstruct Pulmon Dis |
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| Autors principals: | , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Dove
2020
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7735792/ https://ncbi.nlm.nih.gov/pubmed/33328731 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/COPD.S276773 |
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