Showing results (11-20 of 68) with videos related to
Sort By:
Pageof 7
The Journal of General Physiology|April 26, 2006
Soluble mediators, not cilia, determine airway surface liquid volume in normal and cystic fibrosis superficial airway epitheliaRobert Tarran, Laura Trout, Scott H Donaldson, et al.Journal of Aerosol Medicine and Pulmonary Drug Delivery|February 21, 2013
Comparison of 133 xenon ventilation equilibrium scan (XV) and 99m technetium transmission (TT) scan for use in regional lung analysis by 2D gamma scintigraphy in healthy and cystic fibrosis lungsKirby L Zeman, Jihong Wu, Scott H Donaldson, et al.Pediatric Pulmonology|October 2, 2008
Safety and tolerability of inhaled hypertonic saline in young children with cystic fibrosisElisabeth P Dellon, Scott H Donaldson, Robin Johnson, et al.Therapeutic Advances in Respiratory Disease|February 1, 2025
New era, new GOALs: cardiovascular screening and lipid management in cystic fibrosisKatherine A Despotes, Agathe S Ceppe, Jennifer L Goralski, et al.Respiratory Research|October 8, 2016
Effects of inhaled high-molecular weight hyaluronan in inflammatory airway diseaseAdelaida Lamas, Jamie Marshburn, Vandy P Stober, et al.Proceedings of the American Thoracic Society|July 27, 2007
Mucociliary clearance as an outcome measure for cystic fibrosis clinical researchScott H Donaldson, Timothy E Corcoran, Beth L Laube, et al.Pediatric Pulmonology|January 19, 2010
Cystic fibrosis lung disease starts in the small airways: can we treat it more effectively?Harm A W M Tiddens, Scott H Donaldson, Margaret Rosenfeld, et al.The Clinical Respiratory Journal|August 30, 2024
Analysis of Depression and Anxiety Scores Following Initiation of Elexacaftor/Tezacaftor/Ivacaftor in Adults With Cystic FibrosisHarish Pudukodu, Margret Z Powell, Agathe Ceppe, et al.European Respiratory Review : an Official Journal of the European Respiratory Society|September 18, 2024
Neutrophil serine proteases in cystic fibrosis: role in disease pathogenesis and rationale as a therapeutic targetMarcus A Mall, Jane C Davies, Scott H Donaldson, et al.The New England Journal of Medicine|January 20, 2006
Mucus clearance and lung function in cystic fibrosis with hypertonic salineScott H Donaldson, William D Bennett, Kirby L Zeman, et al.Pageof 7