Airway inflammation and infection are present from early in life, often before children are symptomatic.
The presence of Pseudomonas aeruginosa biofilms in lower airway specimens from cystic fibrosis (CF) patients is well established.
Biomarkers in cystic fibrosis are used for the measurement of cystic fibrosis transmembrane regulator function in order to diagnose cystic fibrosis,.…
No evidence to demonstrate relationships with symptoms and viruses, prolonged symptoms, prolonged shedding or patterns of virus infections in CF
A new Australian study that looked at the long term impacts of early lung infections in young kids with cystic fibrosis has recommended changes to mo…
Need for research into family-centred caring as a way of caring for children and families where one or more of the children have cystic fibrosis
Determinants of culture success through retrospective analysis of a program of routinely brushing children with Cystic Fibrosis airway disease
Despite our current treatment, many cystic fibrosis (CF) patients still show progressive bronchiectasis and small airways disease.
This paper is a review of lung function tests best suited to use for early detection of lung disease in Cystic Fibrosis.
This paper is about lung disease in patients with cyctic Fibrosis and prevention strategies to slow the onset of lung disease.