A number of strategies can help to ensure adequate joint care to best manage joint pain and stiffness in Duchenne muscular dystrophy (DMD).

Gene therapy could be the newest breakthrough for Duchenne muscular dystrophy. While it may not be a cure, it can give independence to boys diagnosed with DMD.

Windsor musicians are set to join forces at a charity open mic night, raising funds to help young people living with a rare muscular disorder.

To help neurologists, clinicians and families understand the current evidence for a new gene therapy for Duchenne muscular ...

Scientists present current evidence for a new gene therapy for Duchenne muscular dystrophy called delandistrogene moxeparvovec.

To help neurologists, clinicians and families understand the current evidence for a new gene therapy for Duchenne muscular ...

To help neurologists, clinicians and families understand the current evidence for a new gene therapy for Duchenne muscular dystrophy ...

The CEO at Nottingham-headquartered Blinds 2go is cycling 300km in 24-hours in a bid to raise an impressive £10,000 for ...

The 17-year-old girl was diagnosed with a neuro attack, which landed her on a wheelchair, but her grit and confidence to ...

The National Institute of Allergy and Infectious Diseases (NIAID) plans to initiate phase 1 clinical trial of Capricor's ...

Cas12Max-based gene editing therapy for Duchenne muscular dystrophy, one of the most severe forms of the inherited muscular dystrophies that affects primarily boys. Huidagene Therapeutics and its ...