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Pediatric Pulmonology|April 13, 2012
Clearance of initial mucoid Pseudomonas aeruginosa in patients with cystic fibrosisRobert Bradley Troxler, Wynton C Hoover, LaCrecia J Britton, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|August 13, 2013
Cigarette smoke and CFTR: implications in the pathogenesis of COPDAndras Rab, Steven M Rowe, S Vamsee Raju, et al.
Annals of Epidemiology|October 10, 2013
A semiparametric approach to estimate rapid lung function decline in cystic fibrosisRhonda D Szczesniak, Gary L McPhail, Leo L Duan, et al.
International Journal of Molecular Sciences|January 21, 2023
Phenotypic Alteration of an Established Human Airway Cell Line by Media SelectionGalit Livnat, Jessica D Meeker, Alicia J Ostmann, et al.
Respiratory Care|December 13, 2018
Objective Versus Self-Reported Adherence to Airway Clearance Therapy in Cystic FibrosisGabriela R Oates, Irena Stepanikova, Steven M Rowe, et al.
Nature Reviews. Disease Primers|May 19, 2016
Cystic fibrosisFelix Ratjen, Scott C Bell, Steven M Rowe, et al.
Respiratory Research|February 27, 2014
Acquired defects in CFTR-dependent β-adrenergic sweat secretion in chronic obstructive pulmonary diseaseClifford A Courville, Sherry Tidwell, Bo Liu, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|August 2, 2016
Hyperpolarized 129Xe for investigation of mild cystic fibrosis lung disease in pediatric patientsRobert P Thomen, Laura L Walkup, David J Roach, et al.
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