Continuous glucose monitoring abnormalities in cystic fibrosis youth correlate with pulmonary function decline.
Respiratory rate in infants with cystic fibrosis throughout the first year of life and association with lung clearance index measured shortly after birth
Emergence of livestock-associated MRSA isolated from cystic fibrosis patients: result of a Belgian national survey
Impact of a program ensuring consistent response to acute drops in lung function in children with cystic fibrosis.
Interleukin-1 is associated with inflammation and structural lung disease in young children with cystic fibrosis
Electrochemical measurement of membrane cholesterol correlates with CFTR function and is HDAC6-dependent
Age-Related differences in Dental Caries and Associated Risk Factors in Individuals with Cystic Fibrosis Ages 6-20 years: A Pilot Study
A Specialized Method of Sputum Collection and Processing for Therapeutic Interventions in Cystic Fibrosis
Characteristics and outcomes of oral antibiotic treated pulmonary exacerbations in children with cystic fibrosis.
