Publication | Open Access
Airways in cystic fibrosis are acidified: detection by exhaled breath condensate
249
Citations
25
References
2002
Year
These findings support the hypothesis that airway acidification occurs in CF. This acidity is in part a function of inflammation as the pH of the EBC of patients increased significantly with treatment of an exacerbation, although not to control levels. Acidic pH of the ELF may play a role in the pathophysiology of CF lung disease and requires further investigation.
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