Comparison of Nutrition and Lung Function Outcomes in Patients with Cystic Fibrosis Living in Canada and the United States
Differences in clinical outcomes of paediatric cystic fibrosis patients with and without meconium ileus.
Randomized Controlled Study of Aerosolized Hypertonic Xylitol Versus Hypertonic Saline in Hospitalized Patients with Pulmonary Exacerbation of Cystic Fibrosis
Correspondence between Lung Function and Symptom Measures from the Cystic Fibrosis Respiratory Symptom Diary–Chronic Respiratory Infection Symptom Score (CFRSD-CRISS)
Variation in lung function and nutritional decline in cystic fibrosis by genotype: An analysis of the Canadian Cystic Fibrosis Registry
Impact of a program ensuring consistent response to acute drops in lung function in children with cystic fibrosis.
Characteristics and outcomes of oral antibiotic treated pulmonary exacerbations in children with cystic fibrosis.