Walk into 13-year-old Seton James' room, and you'll see priceless sports memorabilia, proof that dreams really do come true.

The study, titled “Structural and Functional Pulmonary MRI to Predict Pulmonary Exacerbations in Cystic Fibrosis,” analyzed imaging and clinical data from 106 individuals with CF who were imaged and ...

Following initiation of elexacaftor/tezacaftor/ivacaftor, Lung Clearance Index decreases in children with cystic fibrosis, ...

Cystic fibrosis causes a buildup of mucus in the lungs that can lead to infection, and often death in children and young ...

Underlying causes of recurrent pneumonia in children have changed in the last decade, indicating a need for individualized diagnostic approaches.

Confirmed wild-type CFTR delivery and expression in conducting airway cells of patients with class I mutationsKB407 transduction confirmed in all ...

Before Caleigh was even born, serious medical complications were detected on her mother’s ultrasound. “When I was born, they couldn’t tell right away what was wrong, but they realized I was in a lot ...

Peak nasal inspiratory flow (PNIF) measurement was a feasible, noninvasive method for assessing nasal airflow obstruction in children with cystic fibrosis and correlated significantly with nasal ...

1 Department of Interdisciplinary Medicine, Pediatric Unit “B. Trambusti”, Cystic Fibrosis Regional Reference Center, University of Bari “Aldo Moro”, Bari, Italy 2 Department of Biotechnological and ...

Publicly-insured and Hispanic children with cystic fibrosis were at highest risk for receiving inadequate CF liver disease screening. Most children with cystic fibrosis (CF) treated at a San Francisco ...

From a very young age, Morgan Barrett struggled to gain weight despite constantly eating. She also battled a persistent cough that never seemed to go away. Her sister Allison experienced similar ...