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Annals of the American Thoracic Society|September 30, 2016
Constrictive Bronchiolitis in Cystic Fibrosis Adolescents with Refractory Pulmonary DeclineWilliam T Harris, J Todd Boyd, Gary L McPhail, et al.The Lancet. Respiratory Medicine|June 14, 2015
Efficacy and safety of ivacaftor in patients with cystic fibrosis who have an Arg117His-CFTR mutation: a double-blind, randomised controlled trialRichard B Moss, Patrick A Flume, J Stuart Elborn, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|February 12, 2020
Variable cellular ivacaftor concentrations in people with cystic fibrosis on modulator therapyJennifer S Guimbellot, Kevin J Ryan, Justin D Anderson, et al.World Journal of Otorhinolaryngology - Head and Neck Surgery|December 6, 2017
Protective and antifungal properties of Nanodisk-Amphotericin B over commercially available Amphotericin BDo-Yeon Cho, Kyle J Hoffman, Gobind S Gill, et al.The Pediatric Infectious Disease Journal|October 1, 2019
Area Deprivation as a Risk Factor for Methicillin-resistant Staphylococcus aureus Infection in Pediatric Cystic FibrosisGabriela R Oates, William T Harris, Steven M Rowe, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|May 29, 2016
Continuous alternating inhaled antibiotics for chronic pseudomonal infection in cystic fibrosisPatrick A Flume, John P Clancy, George Z Retsch-Bogart, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|June 29, 2020
Fibrocyte accumulation in the lungs of cystic fibrosis patientsRajesh K Kasam, Prathibha R Gajjala, Anil G Jegga, et al.JCI Insight|February 23, 2018
Chronic β2AR stimulation limits CFTR activation in human airway epitheliaJohn J Brewington, Jessica Backstrom, Amanda Feldman, et al.American Journal of Respiratory and Critical Care Medicine|November 16, 2021
Clinical Effectiveness of Elexacaftor/Tezacaftor/Ivacaftor in People with Cystic Fibrosis: A Clinical TrialDavid P Nichols, Alex C Paynter, Sonya L Heltshe, et al.Annals of the American Thoracic Society|August 24, 2016
Ultrashort Echo-Time Magnetic Resonance Imaging Is a Sensitive Method for the Evaluation of Early Cystic Fibrosis Lung DiseaseDavid J Roach, Yannick Crémillieux, Robert J Fleck, et al.Pageof 34