It wasn’t that long ago that Ben Prince-Saxon was struggling to keep up with his mates on the football pitch. He’s now completed 12 marathons in 12 months to raise funds for Cystic Fibrosis New ...

In patients with cystic fibrosis (CF), the occurrence of pulmonary exacerbations requiring intensive therapy (PERITs) was associated with marked decline in lung function that was not always reversed ...

Not long ago, Fred Armisen was reminiscing about the sound-effect LPs he used to stock at the Chicago record store where he worked in the Nineties. These vinyl platters contained all kinds of sounds, ...

Cystic fibrosis was once a dire, likely deadly diagnosis, destroying a patient's ability to breathe and digest food—but a revolutionary new treatment offers reason for hope. And on Thursday the three ...

One of this year's coveted Lasker Awards went to three scientists who helped invent a life-saving treatment for cystic fibrosis, a genetic disease. When you purchase through links on our site, we may ...

Brinsupri (brensocatib) is a new oral medicine approved to treat a long-term lung disease known as non-cystic fibrosis bronchiectasis (NCFB) in adults and children ages 12 or older. It works by ...

July 1 (Reuters) - Vertex Pharmaceuticals (VRTX.O), opens new tab said on Tuesday its next-generation cystic fibrosis treatment has won European Union approval for a rare and progressive genetic ...

Cystic fibrosis (CF) is a genetic disorder that causes thick, sticky mucus to build up in the lungs, digestive system and other organs Morgan Barrett; Brittyn Elizabeth Studios From a very young age, ...

Cystic fibrosis (CF) is a rare autosomal recessive disorder that affects numerous systems of the body. It is a complicated disease that differs from person to person. An autosomal recessive disorder ...

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 ...

Cystic fibrosis is a genetic disorder that affects roughly 40,000 Americans. The condition is caused by a mutation in the patient's cystic fibrosis transmembrane conductance regulator (CFTR) gene, ...

The United States Cystic Fibrosis Foundation released the first guideline on newborn screening for cystic fibrosis (CF), in order to improve timely detection of CF in infants from all racial and ...