Seasonal fluctuation of lung function in cystic fibrosis: A national register-based study in two northern European populations
Use of telavancin in adolescent patients with cystic fibrosis and prior intolerance to vancomycin: A case series.
Combined antifungal therapy is superior to monotherapy in pulmonary scedosporiosis in cystic fibrosis
Prevalence of meconium ileus marks the severity of mutations of the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) gene
Improving performance in the detection and management of cystic fibrosis-related diabetes in the Mountain West Cystic Fibrosis Consortium.
Higher Interleukin-7 serum concentrations in patients with cystic fibrosis correlate with impaired lung function
