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Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|July 28, 2023
Traits, trends and hits of orphan drug designations in cystic fibrosisEnrico Costa, Silvia Girotti, Hendrika A van den Ham, et al.
Pediatric Pulmonology|April 6, 2026
Patient-Derived Intestinal Organoids in the Global Cystic Fibrosis LandscapeSuzanne Kroes, Jennifer L Taylor-Cousar, Marco Zampoli, et al.
Annals of the American Thoracic Society|January 31, 2014
Azithromycin may antagonize inhaled tobramycin when targeting Pseudomonas aeruginosa in cystic fibrosisJerry A Nick, Samuel M Moskowitz, James F Chmiel, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|June 26, 2007
Pharmacological modulation of cGMP levels by phosphodiesterase 5 inhibitors as a therapeutic strategy for treatment of respiratory pathology in cystic fibrosisJens F Poschet, Graham S Timmins, Jennifer L Taylor-Cousar, et al.
The Annals of Otology, Rhinology, and Laryngology|November 13, 2023
Decreases in Rhinology Care Utilization by People with Cystic Fibrosis on Highly Effective Modulator TherapyEthan J Han, Daniel M Beswick, Patricia H Eshaghian, et al.
International Forum of Allergy & Rhinology|December 26, 2023
Chronic rhinosinusitis and olfaction after highly effective modulator therapy: The role of individual sinus inflammationJessa E Miller, Jennifer L Taylor-Cousar, Stephen M Humphries, et al.
Antimicrobial Agents and Chemotherapy|September 4, 2014
Enhanced in vitro formation and antibiotic resistance of nonattached Pseudomonas aeruginosa aggregates through incorporation of neutrophil productsSilvia M Caceres, Kenneth C Malcolm, Jennifer L Taylor-Cousar, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|July 25, 2022
Clinician attitudes and practices on pregnancy planning and care in cystic fibrosisKristina Montemayor, Traci M Kazmerski, Kristin A Riekert, et al.
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