Children | European Cystic Fibrosis Society (ECFS)

Lung function and imaging outcomes in children with cystic fibrosis diagnosed after newborn screening

Markers of inflammation in lung fluid can predict lung damage in young children with Cystic Fibrosis (CF)?

Improvement of Pulmonary Function After Implementation of a Standardized Cystic Fibrosis Care Algorithm

Airway infection increases Pseudomonas aeruginosa acquisition

Advanced but not mild liver disease is a predictor of decreased survival in children with cystic fibrosis, with far greater impact in females: A 27-year real-life cohort study

Neutrophils do not produce more oxidants when stimulated to fight infections in cystic fibrosis

A simple blood test to detect how severe liver disease is in children with CF

Evaluating the sodium status in relation to your age will be possible with a single spot urine.

Lung infection by Pseudomonas aeruginosa in children with cystic fibrosis: risk factors and impact on lung function

Experience of COVID-19 during the first wave in children with cystic fibrosis worldwide.

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