She was diagnosed with cystic fibrosis – an inherited condition that causes mucus buildup in the lungs, and often leads to ...

lung transplant candidates with cystic fibrosis had maintained or increased their rehabilitation measures, according to study data. “The present study highlights the importance of physiological ...

Ms Pierce's lung function improved dramatically - from 55% to 71% - her condition is now much more stable and her visits to hospital less frequent. Cystic fibrosis is the most common inherited ...

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

Cahir O'Hagan was 25 when he died from cystic fibrosis while waiting for a lung transplant. A man whose brother died waiting on a double lung transplant says more work is needed to make Cystic ...

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 ...

Announcing a new article publication for BIO Integration journal. Pulmonary fibrosis (PF) is a progressive interstitial lung disease characterized by excessive extracellular matrix deposition and ...

FRESNO, Calif. (KFSN) -- Cystic Fibrosis is a genetic disorder that affects the lungs, digestive system and other organs. Babies are screened for it when they are born. Now, those living with the ...

Cystic fibrosis is a multi-organ disease that primarily affects the lungs and digestive system. In recent years, advances in treatment have meant people are living longer with the condition.