An 8-year-old northern Minnesota boy is one of the first in the country to receive a specific type of gene therapy treatment.

Amid readouts from the Muscular Dystrophy Association’s annual meeting, the Clinical Trials Arena evaluates five DMD trials ...

The beginning to the year has been eventful in the Duchenne muscular dystrophy (DMD ... attending physician at the Children's Hospital of Philadelphia, John Brandsema commented that stem-cell ...

The Cambridge-based biotech's experimental treatment for Duchenne muscular dystrophy hit the mark in a mid-stage study, ...

Wave Life Sciences’ experimental treatment for Duchenne muscular dystrophy hit the mark in a mid-stage study, setting the ...

The 11-year-old's strength and bravery in living with the impact of the serious muscle-wasting condition was hailed by her ...

Several companies will head to the FDA seeking approval of new Duchenne muscular dystrophy treatments next year but the death ...

Convener of Stirling Council’s Children and Young People Committee, Cllr Danny Gibson said: “Somhairle’s bravery, inner ...

There were six awards presented, celebrating success in volunteering, fundraising, caring, community engagement and research, ...

WVE-N531, an oligonucleotide, elicited significant functional benefit and reversal of muscle damage in the Phase II ...

When William's 10th birthday approached, Conde reached out to Little Treasures, the pediatric program for Treasure Coast ...