A new study supports the clinical utility of human nasal epithelial cultures as predictive biomarkers for cystic fibrosis ...

Purpose. The successful use of inhaled morphine to relieve dyspnea in a patient with end-stage cystic fibrosis (CF) lung disease is described. Dyspnea, the sensation of breathlessness or labored ...

MONDAY, April 14, 2025 (HealthDay News) -- Current newborn screening for cystic fibrosis favors white children over those ...

While many of the patients that come through the UCSF Fresno Cystic Fibrosis Center are still young, they have transitioned ...

With this approval, the indication has been expanded to include all patients ages 2 years and older who have at least one non-class I mutation in the cystic fibrosis conductance regulator (CFTR ...

CF is caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. Although recent advancements in CFTR modulator therapies have improved outcomes for many people ...