In patients with CF, pre-transplant PH is associated with improved early post-transplant survival, but with poorer outcomes after 3 years.
Cystic fibrosis (CF) mucus can clog the lungs and digestive tract. Although there is no cure for CF, medications and therapies can help thin this mucus. Share on Pinterest ArtMarie/Getty Images Cystic ...
Supportive therapy, like medications to help open the airways and heal infections, can help you live a healthier life and meet many of the challenges of this inherited respiratory condition. Share on ...
Please provide your email address to receive an email when new articles are posted on . Researchers captured exercise capacity measures during the first week of pulmonary rehabilitation to the session ...
Cystic fibrosis is one of the most common genetic disorders, causing thick mucus build-up in the lungs and other parts of the body, breathing problems, and infection. A three-drug cocktail known as ...
UCLA researchers use lipid nanoparticles to insert full CFTR gene into airway cells, restoring function and opening new avenues for CF therapy.
A 26-year-old woman with cystic fibrosis successfully received her third pair of donor lungs after begging doctors to take her case and give her another shot at life. Taylor Stephenson — whose own ...
PHILADELPHIA (CBS) -- A desperate fight for life for a young woman in Montgomery County. She needs a lung transplant but has been rejected by most hospitals. Follow the tubing to 22-year-old Jen ...
The development of gene editing tools, which enable the specific targeting and correction of mutations, hold the promise of allowing us to correct those mutations that cause genetic diseases. However, ...
After NFL quarterback Boomer Esiason's son was diagnosed with cystic fibrosis, it put a face on a little-known disease and ...
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