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Thorax|November 22, 2019
One-year outcomes in a multicentre cohort study of incident rare diffuse parenchymal lung disease in children (ChILD)Steve Cunningham, Catriona Graham, Morag MacLean, et al.
ERJ Open Research|July 22, 2021
Clinical and research priorities for children and young people with bronchiectasis: an international roadmapAnne B Chang, Jeanette Boyd, Leanne Bell, et al.
Lancet (London, England)|March 15, 2024
Lung-function trajectories: relevance and implementation in clinical practiceErik Melén, Rosa Faner, James P Allinson, et al.
Science Immunology|September 9, 2018
Inception of early-life allergen-induced airway hyperresponsiveness is reliant on IL-13+CD4+ T cellsSejal Saglani, Lisa G Gregory, Avneet K Manghera, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|June 10, 2019
Abnormal pro-gly-pro pathway and airway neutrophilia in pediatric cystic fibrosisAndrew R Turnbull, Chloe J Pyle, Dhiren F Patel, et al.
ERJ Open Research|September 23, 2020
Access to medicines for rare diseases: beating the drum for primary ciliary dyskinesiaSuzanne Crowley, Inês Azevedo, Mieke Boon, et al.
The Lancet. Respiratory Medicine|December 9, 2023
A core outcome set for bronchiectasis in children and adolescents for use in clinical research: an international consensus studyAnne B Chang, Jeanette Boyd, Andrew Bush, et al.
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