Lung clearance index: Evidence for use in clinical trials in cystic fibrosis
Open Access
- 6 December 2013
- journal article
- review article
- Published by Elsevier BV in Journal of Cystic Fibrosis
- Vol. 13 (2), 123-138
- https://doi.org/10.1016/j.jcf.2013.09.005
Abstract
No abstract availableFunding Information
- NIHR Respiratory Biomedical Research Unit
This publication has 63 references indexed in Scilit:
- Multiple Breath Nitrogen Washout: A Feasible Alternative to Mass SpectrometryPLOS ONE, 2013
- A Realistic Validation Study of a New Nitrogen Multiple-Breath Washout SystemPLOS ONE, 2012
- Long-term course of lung clearance index between infancy and school-age in cystic fibrosis subjectsJournal of Cystic Fibrosis, 2011
- Air Trapping on Chest CT Is Associated with Worse Ventilation Distribution in Infants with Cystic Fibrosis Diagnosed following Newborn ScreeningPLOS ONE, 2011
- Multicenter Evaluation of Infant Lung Function Tests as Cystic Fibrosis Clinical Trial EndpointsAmerican Journal of Respiratory and Critical Care Medicine, 2010
- Long-term gas exchange characteristics as markers of deterioration in patients with cystic fibrosisRespiratory Research, 2009
- Lung Volume, Breathing Pattern and Ventilation Inhomogeneity in Preterm and Term InfantsPLOS ONE, 2009
- Ventilation heterogeneity is a major determinant of airway hyperresponsiveness in asthma, independent of airway inflammationThorax, 2007
- Early detection of cystic fibrosis lung disease: multiple-breath washout versus raised volume testsThorax, 2007
- Biomarkers and surrogate endpoints: Preferred definitions and conceptual frameworkClinical Pharmacology & Therapeutics, 2001