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 claims-based study revealed high adherence to phosphorodiamidate morpholino oligomer (PMO) treatments for Duchenne muscular dystrophy (DMD), but highlights limitations in interpreting real-world ...

DMD is a genetic disorder, predominantly affecting males, entailing irreversible muscle degeneration. Maldonado underwent ...

Clinical development and trial testing of vesleteplirsen (SRP-5051) for Duchenne muscular dystrophy (DMD) was stopped, with ...

In-shoe sensors, AI and biomarkers will monitor muscular dystrophy and atrophy in children, adolescents and adults — with ...

Scientists have been searching for ways to cure DMD for as long as they have known about the disease. Today, based on the wealth of knowledge about the underlying genetic and molecular mechanisms ...

Duchenne Muscular Dystrophy is a genetically inherited disorder that causes muscles to progressively weaken and waste. It is X-linked, where sons inherit it from their mothers, or in rare ...

Duchenne Muscular Dystrophy is a genetically inherited disorder that causes muscles to progressively weaken and waste. It is X-linked, where sons inherit it from their mothers, or in rare ...

Roche-partnered SRP-9001 (delandistrogene moxeparvovec) has been submitted for approval to treat ambulatory (walking) patients with DMD, a genetic disorder characterised by progressive muscle ...