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Improving Screening for Alpha-1 Antitrypsin Deficiency with Direct Testing in the Pulmonary Function Testing Laboratory
Alpha-1 antitrypsin deficiency (AATD) is a common but highly underdiagnosed genetic disorder that may lead to chronic obstructive pulmonary disease (COPD), bronchiectasis, and liver disease. Early diagnosis is key to altering the course of disease as well as informing family members of potential ris...
Guardat en:
| Publicat a: | Chronic Obstr Pulm Dis |
|---|---|
| Autors principals: | , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
COPD Foundation Inc
2021
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8237974/ https://ncbi.nlm.nih.gov/pubmed/33290644 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.15326/jcopdf.2020.0179 |
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