Muscular Dystrophy UK is the leading charity for more than 110,000 children and adults in the UK living with one of over 60 ...

The FDA has granted Orphan Drug and Rare Pediatric Disease Designations to Somite’s cell replacement therapy for the ...

The Billings Livestock Commission hosted the sixth annual Calves to Cure to help raise money and awareness for Duchenne ...

ABOUT PARENT PROJECT MUSCULAR DYSTROPHY Duchenne is a genetic disorder that slowly robs people of their muscle strength. Parent Project Muscular Dystrophy (PPMD) fights every single battle ...

To provide hope for families grappling with Duchenne muscular dystrophy across Upstate New York, Buffalo-based Suneel’s Light Foundation has launched a new community grant program, Brighter Days Commu ...

Somite Therapeutics, a fully integrated TechBio company leveraging big data and AI to introduce novel cell replacement therapies, today announced that the U.S. Food and Drug Administration (FDA) has ...

The embryos were female, and Jenssen remembers the doctors assuring her that, because the Duchenne mutation is linked to the ...

Avidity supports World Duchenne Awareness Day, International Myotonic Dystrophy Awareness Day, FSHD Society Walk & Roll to Cure FSHD and Global Genes Week in RARE SAN DIEGO, Sept. 5, 2024 /PRNewswire/ ...

World Duchenne Awareness Day is celebrated on September 7th every year Here’s Why Soda Cans Are Beveled on the Bottom See the ...

A Northern Ireland man, 31, with Duchenne Muscular Dystrophy – a progressive muscle wasting disease that affects skeletal ...

AI-driven biotech Somite.ai scores dual FDA designations for its novel treatment, potentially fast-tracking hope for families ...

Progress in health and social care in European countries is helping many boys with Duchenne muscular dystrophy (DMD ... views on how to improve lives of people with the condition across Europe.