The Lancet Respiratory Medicine · 2013 · 224 citations · 22 references
MedicineClinical SciencesPharmacotherapyPulmonary Function TestingPulmonologyCystic FibrosisCystic Fibrosis PharmacotherapyMucociliary ClearancePulmonary AssessmentPulmonary Function AssessmentRespiratory MonitoringCftr Gene MutationsCftr Protein FunctionClearance In The LungCystic Fibrosis GeneticsCystic Fibrosis Lung DiseaseDurable Clinical ResponseIvacaftor TherapyPharmacodynamics In Cystic Fibrosis
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Changes in the normal maximal expiratory flow-volume curve with growth and aging.
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