Lung function and imaging outcomes in children with cystic fibrosis diagnosed after newborn screening
Markers of inflammation in lung fluid can predict lung damage in young children with Cystic Fibrosis (CF)?
Improvement of Pulmonary Function After Implementation of a Standardized Cystic Fibrosis Care Algorithm
Advanced but not mild liver disease is a predictor of decreased survival in children with cystic fibrosis, with far greater impact in females: A 27-year real-life cohort study
Lung infection by Pseudomonas aeruginosa in children with cystic fibrosis: risk factors and impact on lung function
