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Microstructural alterations of sputum in cystic fibrosis lung disease
The stasis of mucus secretions in the lungs of cystic fibrosis (CF) patients leads to recurrent infections and pulmonary exacerbations, resulting in decreased survival. Prior studies have assessed the biochemical and biophysical features of airway mucus in individuals with CF. However, these measure...
Guardat en:
| Publicat a: | JCI Insight |
|---|---|
| Autors principals: | , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
American Society for Clinical Investigation
2016
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5085601/ https://ncbi.nlm.nih.gov/pubmed/27812540 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/jci.insight.88198 |
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