Chloride Conductance, Nasal Potential Difference and Cystic Fibrosis Pathophysiology
Author:
Funder
Hospital de Clínicas de Porto Alegre
Publisher
Springer Science and Business Media LLC
Subject
Pulmonary and Respiratory Medicine
Link
http://link.springer.com/content/pdf/10.1007/s00408-019-00293-6.pdf
Reference29 articles.
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2. Liou TG (2019) The clinical biology of cystic fibrosis transmembrane regulator protein: its role and function in extrapulmonary disease. Chest 155(3):605–616
3. Quinton PM (2017) Both ways at once: keeping small airways clean. Physiology (Bethesda) 32(5):380–390
4. Tang XX, Ostedgaard LS, Hoegger MJ, Moninger TO, Arp PH, McMenimen JD et al (2016) Acidic pH increases airway surface liquid viscosity in cystic fibrosis. J Clin Invest 126:879–891
5. Rubin BK (2018) Unmet needs in cystic fibrosis. Expert Opin Biol Ther 8:49–52
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