Molecular characterization of gene regulatory networks in primary human tracheal and bronchial epithelial cells.
Development and electronic validation of the revised Cystic Fibrosis Questionnaire (CFQ-R Teen/Adult): New tool for monitoring psychosocial health in CF.
The relationship between sweat chloride levels and mortality in cystic fibrosis varies by individual genotype.
Implementing the International Committee on Mental Health in Cystic Fibrosis (ICMH) Guidelines: Screening accuracy and referral-treatment pathways
Early detection using qPCR of Pseudomonas aeruginosa infection in children with cystic fibrosis undergoing eradication treatment
