The CF Canada-Sick Kids Program in individual CF therapy: A resource for the advancement of personalized medicine in CF.
Mini-guts in a dish: Perspectives of adult Cystic Fibrosis (CF) patients and parents of young CF patients on organoid technology
Defining Research Priorities in Cystic Fibrosis. Can Existing Knowledge and Training in Biomedical Research affect the Choice?
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
