Duchenne Muscular Dystrophy: diagnosis, clinical development and global researchMuscular dystrophy refers to a group of rare, genetic, progressive diseases that primarily affect the body’s muscles, ...

Newborn screening is also cost-effective. Testing that takes just a few dollars per baby can save families and the health ...

Multidisciplinary coordination across prescribing teams, nursing, laboratory medicine, finance, and infusion centers is crucial for gene therapy delivery in Duchenne muscular dystrophy (DMD).

Two dose levels of a single-administration gene therapy were well-tolerated and led to functional improvements in ambulatory ...

A major trial of a promising gene therapy for Duchenne muscular dystrophy has fallen short, but researchers say the lessons learned could pave the way for better, more effective treatments.

A trial found magnetic resonance imaging correlated with physical function tests in patients with Duchenne muscular dystrophy ...

A Southern Oregon family is embarking on a remarkable journey to support their son, who is facing a life-threatening disease.

The remote measurement tool enables Duchenne muscular dystrophy (DMD) assessments through analysis of caregiver-recorded ...

The NHS has rolled out a new treatment for muscular degeneration at a few sites in England and Wales, while Scotland and Northern Ireland do not have access. | ITV National News ...

Health Secretary Neil Gray has been criticised for posting about football and traffic lights on social media while failing to ...

Kyle had nominated his parents, David and Kristen Cox, to be Texas A&M’s Parents of the Year.