Cystic fibrosis (CF) is a genetic disease characterized by dehydration of airway surface liquid
and impaired mucociliary clearance. As a result, there is difficulty clearing pathogens from …

Rationale: Cystic fibrosis is a recessive genetic disease characterized by dehydration of the
airway surface liquid and impaired mucociliary clearance. As a result, individuals with the …

Background Patients with cystic fibrosis have altered levels of plasma fatty acids. We
previously demonstrated that arachidonic acid levels are increased and docosahexaenoic acid …

… O'Sullivan and coworkers (47) showed that washed platelets … O'Sullivan and coworkers
(47) also observed a decreased … As discussed above, O'Sullivan and coworkers (47) …

Background Reducing treatment burden is a priority for people with cystic fibrosis, whose
health has benefited from using new modulators that substantially increase CFTR protein …

… O'Sullivan and Jessica Snowden: lead conception and drafting of the work; final approval
of the version published. Laura James and Joseph M. Majure: substantial contribution to the …

Objectives. Newborn screening for cystic fibrosis (CF) provides a model to investigate the
implications of applying multiple-mutation DNA testing in screening for any disorder in a …

Newborn screening for cystic fibrosis offers the opportunity for early intervention and improved
outcomes. This summary, resulting from a workshop sponsored by the Cystic Fibrosis …

Tracheal bronchus is a common anomaly that occurs in approximately 2% of people. Two
children with multiple medical problems which led to endotracheal intubation are described. …

Patients with cystic fibrosis (CF) exhibit an excessive host inflammatory response. The aim
of this study was to determine (i) whether interleukin 8 (IL-8) secretion is increased from …