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Journal of Paediatrics and Child Health|July 15, 2005
Pubertal development and its influences on bone mineral density in Australian children and adolescents with cystic fibrosisHelen M Buntain, Ristan M Greer, Joseph C H Wong, et al.
The Lancet. Respiratory Medicine|June 11, 2018
Ivacaftor treatment of cystic fibrosis in children aged 12 to <24 months and with a CFTR gating mutation (ARRIVAL): a phase 3 single-arm studyMargaret Rosenfeld, Claire E Wainwright, Mark Higgins, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|August 21, 2025
Validation of an artificial intelligence-based automated PRAGMA and mucus plugging algorithm in pediatric cystic fibrosisPranali Raut, Yuxin Chen, Ahmad Taleb, et al.
Respirology (Carlton, Vic.)|December 30, 2015
Pseudomonas aeruginosa antibiotic resistance in Australian cystic fibrosis centresDaniel J Smith, Kay A Ramsay, Stephanie T Yerkovich, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|April 22, 2017
CFTR-dependent defect in alternatively-activated macrophages in cystic fibrosisAbdullah A Tarique, Peter D Sly, Patrick G Holt, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|August 13, 2016
The changing prevalence of pulmonary infection in adults with cystic fibrosis: A longitudinal analysisKay A Ramsay, Harpreet Sandhu, James B Geake, et al.
Respirology (Carlton, Vic.)|September 11, 2009
Multi-centre research in Australia: analysis of a recent National Health and Medical Research Council-funded projectTimothy J Kidd, Guy B Marks, Peter T P Bye, et al.
American Journal of Respiratory and Critical Care Medicine|October 7, 2020
Ivacaftor in Infants Aged 4 to <12 Months with Cystic Fibrosis and a Gating Mutation. Results of a Two-Part Phase 3 Clinical TrialJane C Davies, Claire E Wainwright, Gregory S Sawicki, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|January 30, 2025
Tolerability and effectiveness of face-masks in reducing cough aerosols for children with cystic fibrosisGeorge T P Tay, Kim Smith, Congrong He, et al.
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