CT evaluation of hyperattenuating mucus to diagnose allergic bronchopulmonary aspergillosis in the special condition of cystic fibrosis
Assessment of stability and fluctuations of cultured lower airway bacterial communities in people with cystic fibrosis
The Cystic Fibrosis Foundation Patient Registry. Design and Methods of a National Observational Disease Registry
Genome-wide association meta-analysis identifies five modifier loci of lung disease severity in cystic fibrosis
Assessment of safety and efficacy of long-term treatment with combination lumacaftor and ivacaftor therapy in patients with cystic fibrosis homozygous for the F508del-CFTR mutation (PROGRESS): a phase 3, extension study.
