People living with cystic fibrosis (CF) will benefit from improved treatment as international experts produce clinical practice guidance for exercise assessments.
Aug 9, 2023
0
7
New research by the Pragmatic Health Ethics Research Unit of the Montreal Clinical Research Institute (IRCM), affiliated with University of Montreal, highlights the colossal challenges faced by people living with one or more ...
Aug 8, 2023
0
7
Newborn screening for cystic fibrosis (CF) was fully implemented in all 50 states in the U.S. by 2010, but delays in timeliness of evaluation for infants with positive newborn screen tests persist. Through evaluation of national ...
Jul 31, 2023
0
1
A scorpionfish protein could prove a powerful tool for treating multidrug-resistant bacterial infections in people with cystic fibrosis, according to a preliminary study published today in eLife.
Jul 18, 2023
0
18
The mucus in the airways is not as sticky, and inflammation in the lungs is significantly reduced: Triple combination therapy can achieve these positive, lasting effects in patients with cystic fibrosis (CF). Researchers ...
Jul 7, 2023
0
10
Cystic fibrosis (CF) is one of the most common genetic disorders in the world. The disease infects nearly 70,000 people worldwide and approximately one in 30 Americans is a carrier. CF is caused by mutations in the human ...
May 22, 2023
0
8
Patients with cystic fibrosis (CF) face difficulty breathing and a decline in lung function and are at risk of early death. CF is an inherited condition that results in thick mucus build-up, persistent infection and inflammation ...
Mar 15, 2023
0
11
Barely a month goes by without headlines announcing yet another advancement in cancer vaccines.
Mar 7, 2023
0
2
Southampton clinical researchers, working as part of a UK team, have shed new light on causes of bronchiectasis, a long-term lung condition currently effecting more than 200,000 people in the UK.
Dec 20, 2022
0
31
UK health authorities on Tuesday announced a pioneering research programme using the genomes of 100,000 new-born babies, to detect rare genetic illnesses and speed up treatment.
Dec 13, 2022
0
3
