[HTML][HTML] An ex vivo rat trachea model reveals abnormal airway physiology and a gland secretion defect in cystic fibrosis
E Harris, M Easter, J Ren, S Krick, J Barnes, SM Rowe - Plos one, 2023 - journals.plos.org
Cystic fibrosis (CF) is a genetic disease hallmarked by aberrant ion transport that results in
delayed mucus clearance, chronic infection, and progressive lung function decline. Several …
delayed mucus clearance, chronic infection, and progressive lung function decline. Several …
[PDF][PDF] The use of miramistin in the treatment of chronic gingivitis in children with cystic fibrosis
M Tkachenko, Y Fomenko… - …, 2021 - pharmacologyonline.silae.it
The study involved an assessment of the time course of hygienic, periodontal indices and
criteria of local immunity of the oral cavity in children with cystic fibrosis, secondary to …
criteria of local immunity of the oral cavity in children with cystic fibrosis, secondary to …
[引用][C] 176 Cystic fibrosis airway inflammation enhances the efficacy of CFTR modulators
C Ribeiro, J Minges, N Quinney, S Boyles… - Journal of Cystic …, 2023 - Elsevier