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Pediatric Nephrology (Berlin, Germany)|April 28, 2015
Risk factors for acute kidney injury during aminoglycoside therapy in patients with cystic fibrosisKevin J Downes, Neha R Patil, Marepalli B Rao, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|April 20, 2022
Effects of ivacaftor on systemic inflammation and the plasma proteome in people with CF and G551DJordana E Hoppe, Brandie D Wagner, J Kirk Harris, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|September 15, 2023
SNSP113 (PAAG) improves mucociliary transport and lung pathology in the Scnn1b-Tg murine model of CF lung diseaseElex S Harris, Lea Novak, Courtney M Fernandez-Petty, et al.
The European Respiratory Journal|April 1, 2023
Cystic fibrosis transmembrane conductance regulator in COPD: a role in respiratory epithelium and beyondMarcus A Mall, Gerard J Criner, Marc Miravitlles, et al.
The Lancet. Respiratory Medicine|June 15, 2016
Pulmonary artery enlargement and cystic fibrosis pulmonary exacerbations: a cohort studyJ Michael Wells, Roopan F Farris, Taylor A Gosdin, et al.
The European Respiratory Journal|February 4, 2022
Static mucus impairs bacterial clearance and allows chronic infection with Pseudomonas aeruginosa in the cystic fibrosis ratAlexander G Henderson, Joy M Davis, Johnathan D Keith, et al.
Pediatric Pulmonology|August 4, 2022
Plasma and cellular ivacaftor concentrations in patients with cystic fibrosisJennifer S Guimbellot, Kevin J Ryan, Justin D Anderson, et al.
American Journal of Audiology|January 19, 2021
Functional Impacts of Aminoglycoside Treatment on Speech Perception and Extended High-Frequency Hearing Loss in a Pediatric Cystic Fibrosis CohortChelsea M Blankenship, Lisa L Hunter, M Patrick Feeney, et al.
Plos One|October 1, 2014
Tgf-beta downregulation of distinct chloride channels in cystic fibrosis-affected epitheliaHongtao Sun, William T Harris, Stephanie Kortyka, et al.
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