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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...
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| Publicado no: | Chronic Obstr Pulm Dis |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
COPD Foundation Inc
2021
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| Assuntos: | |
| Acesso em linha: | 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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