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The Cystic Fibrosis Trust (stylised as Cystic Fibrosis) is a UK-based national charity founded in 1964, dealing with all aspects of cystic fibrosis (CF). It funds research to treat and cure CF and aims to ensure appropriate clinical care and support for people with cystic fibrosis.
Cystic Fibrosis Trust, [12] a UK charity providing research, information and care for people with cystic fibrosis DCFH - Deutsche CF-Hilfe - Unterstützung für Menschen mit Mukoviszidose e.V., [ 13 ] a German-based patient organization to support people with cystic fibrosis
In the video, dad Duane spoke about the Trust’s pioneering research into treating the illness. The parents of a four-year-old boy with cystic fibrosis, whose gene pairing makes him “one of 50 ...
Commenting on the announcement, David Ramsden, chief executive at the Cystic Fibrosis Trust, said: “This is great news and another important step in ensuring access to life-changing modulator ...
Cystic fibrosis (also known as CF or mucoviscidosis) is an autosomal recessive genetic disorder affecting most critically the lungs, and also the pancreas, liver, and intestine.
Crohn's and Colitis UK; Crossroads Care; Cystic Fibrosis Trust; D. David Lewis Centre; Deafblind UK; Deafness Research UK; DEBRA; Defence Medical Welfare Service;
Davies investigates cystic fibrosis. She was involved with a major UK trial of gene therapy for cystic fibrosis. [8] Davies leads the Strategic Research Centre for Pseudomonas Infection in Cystic Fibrosis at Imperial College London, one of few centres supported by the Cystic Fibrosis Trust. [9]
After leaving politics Barnes became a charity director, first for the Royal College of Obstetricians and Gynaecologists at Birthright (which she renamed WellBeing), and subsequently as Chief Executive of the Cystic Fibrosis Trust which she joined in October 1996 and from which she retired in August 2010.