Latest Becker's muscular dystrophy Stories
Recent scientific development represents progress in FSHD research. Lexington, Mass.
A preclinical study led by researchers at Children’s National Medical Center has found that a new oral drug shows early promise for the treatment of Duchenne muscular dystrophy (DMD).
Children with Duchenne muscular dystrophy often die as young adults from heart and breathing complications.
Using a novel genetic 'editing' technique, Duke University biomedical engineers have been able to repair a defect responsible for one of the most common inherited disorders, Duchenne muscular dystrophy, in cell samples from Duchenne patients.
- a slit in a tire to drain away surface water and improve traction.