Decline in Forced Expiratory Volume in 1 Second in Cystic Fibrosis—Watch the Pendulum Swing
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology, and Child Health
Reference18 articles.
1. Endpoints for clinical trials in young children with cystic fibrosis;Davis;Proc Am Thorac Soc,2007
2. Reduced lung function in cystic fibrosis: a primary or secondary phenotype?;Davis;Am J Respir Crit Care Med,2008
3. Pseudomonas aeruginosa and other predictors of mortality and morbidity in young children with cystic fibrosis;Emerson;Pediatr Pulmonol,2002
4. Genetic modifiers of lung disease in cystic fibrosis;Drumm;N Engl J Med,2005
5. Chronic Stenotrophomonas maltophilia infection and exacerbation outcomes in cystic fibrosis;Waters;J Cyst Fibros,2012
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. An 8 week open-label interventional multicenter study to explore the lung clearance index as endpoint for clinical trials in cystic fibrosis patients ≥8 years of age, chronically infected with Pseudomonas aeruginosa;BMC Pulmonary Medicine;2020-06-12
2. Forced expiratory volume in 1 second variability in cystic fibrosis—has the clinical utility been lost in statistical translation?;The Journal of Pediatrics;2016-05
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