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.

Michelle C. Werner agonized over whether the gene therapy treatment Elevidys was right for her teenage son. But to him, the ...

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

Duchenne Muscular Dystrophy is a rare progressive disorder. People with DMD are missing muscle-protecting protein, due to a fault in the gene producing dystrophin. Muscles become weaker over time ...

We hypothesize that Duchenne muscular dystrophy and autism spectrum disorder/pervasive developmental disorder co-occur with a greater than random frequency. In this study, we set out to reject the ...

A pilot study using a new screening tool shows promise for assessing neurobehavioral difficulties in children with Duchenne muscular dystrophy (DMD) and improving quality of life for patients and ...

The Neu-REFIX Beta 1,3-1,6 glucan, is an exo-polysaccharide produced by N-163 strain of Aureobasidium Pullulans, available as ...

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 ...

When George Stalley was just 18-months-old, his mum and dad Kathy and Glenn were given news no parent wants to hear, told to ...

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 ...

KUWAIT, Sept 11: Dr. Laila Bastaki, Head of the Genetic Diseases Center at the Ministry of Health, emphasized the importance of incorporating genetic testing for Duchenne muscular dystrophy (DMD) into ...

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/ ...