Reduced Lung Function in Cystic Fibrosis
Author:
Publisher
American Thoracic Society
Subject
Critical Care and Intensive Care Medicine,Pulmonary and Respiratory Medicine
Reference15 articles.
1. Endpoints for Clinical Trials in Young Children with Cystic Fibrosis
2. The lung in cystic fibrosis
3. The Evolution of Airway Function in Early Childhood Following Clinical Diagnosis of Cystic Fibrosis
4. Airway function in infants newly diagnosed with cystic fibrosis
5. Gas trapping in normal infants and in infants with cystic fibrosis
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1. Synergy between Readthrough and Nonsense Mediated Decay Inhibition in a Murine Model of Cystic Fibrosis Nonsense Mutations;International Journal of Molecular Sciences;2020-12-31
2. Linaclotide improves gastrointestinal transit in cystic fibrosis mice by inhibiting sodium/hydrogen exchanger 3;American Journal of Physiology-Gastrointestinal and Liver Physiology;2018-11-01
3. Decline in Forced Expiratory Volume in 1 Second in Cystic Fibrosis—Watch the Pendulum Swing;The Journal of Pediatrics;2016-02
4. Clinical Significance of Microbial Infection and Adaptation in Cystic Fibrosis;Clinical Microbiology Reviews;2011-01
5. Potential misinterpretation of infant lung function unless prospective healthy controls are studied;Pediatric Pulmonology;2010-07-20
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