Cirrhosis associated with decreased survival and a 10-year lower median age at death of cystic fibrosis patients in the Netherlands
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
