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Alpha 1 “Hereditary Emphysema” Experience: A Patient–Physician Perspective
This article is co-authored by a patient living with alpha-1 antitrypsin deficiency, and her treating physician. The commentary article describes the patient’s experience of the diagnosis and treatment process. The physician then discusses alpha-1 antitrypsin deficiency diagnosis and management in t...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Springer Healthcare
2020
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7672128/ https://www.ncbi.nlm.nih.gov/pubmed/32519167 http://dx.doi.org/10.1007/s41030-020-00119-4 |