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American Journal of Respiratory and Critical Care Medicine|March 18, 2021
A Phase 3 Open-Label Study of Elexacaftor/Tezacaftor/Ivacaftor in Children 6 through 11 Years of Age with Cystic Fibrosis and at Least One <i>F508del</i> AlleleEdith T Zemanick, Jennifer L Taylor-Cousar, Jane Davies, et al.Pediatric Pulmonology|February 4, 2025
SHIFTing goals in cystic fibrosis-managing extrapulmonary disease in the era of CFTR modulator therapy; Proceedings of the International Shaping Initiatives and Future Trends (SHIFT) SymposiumJonathan E M O'Donnell, Lucy A Hastings, Julie N Briody, et al.American Journal of Respiratory and Critical Care Medicine|July 11, 2022
Efficacy and Safety of Elexacaftor/Tezacaftor/Ivacaftor in Children 6 Through 11 Years of Age with Cystic Fibrosis Heterozygous for <i>F508del</i> and a Minimal Function Mutation: A Phase 3b, Randomized, Placebo-controlled StudyMarcus A Mall, Rossa Brugha, Silvia Gartner, et al.Ebiomedicine|July 5, 2025
Phase 2a/b randomised placebo-controlled dose-escalation trial of triheptanoin for ataxia-telangiectasia: treating mitochondrial dysfunction with anaplerosisMatthew Lynch, Sophie Manoy, Peter D Sly, et al.Science (New York, N.Y.)|November 16, 2016
Emergence and spread of a human-transmissible multidrug-resistant nontuberculous mycobacteriumJosephine M Bryant, Dorothy M Grogono, Daniela Rodriguez-Rincon, et al.Nature Ecology & Evolution|July 23, 2021
Drivers of seedling establishment success in dryland restoration effortsNancy Shackelford, Gustavo B Paterno, Daniel E Winkler, et al.Pageof 10