Isogenic cell models of cystic fibrosis-causing variants in natively expressing pulmonary epithelial cells.
Application of Multiple Event Analysis as an alternative approach to studying pulmonary exacerbations as an outcome measure
Abnormal Preschool Lung Clearance Index (LCI) reflects clinical status and predicts lower spirometry later in childhood in Cystic Fibrosis.
Antibody response against Mycobacterium avium complex in cystic fibrosis patients measured by a novel IgG ELISA test
Social Support is Associated with Fewer Reported Symptoms and Decreased Treatment Burden in Adults with Cystic Fibrosis
Visceral Adipose Tissue is Associated with Poor Diet Quality and Higher Fasting Glucose in Adults with Cystic Fibrosis
