gstt.sthames.nhs.uk Although bladder function is thought to be unaffected in Duchenne muscular dystrophy, 46/88 boys interviewed had urinary problems. Nine underwent video urodynamics, showing in ...

An infant named KJ has made history as the first patient to be treated with an in vivo CRISPR gene editing therapy designed ...

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

Earlier this year, Una Ennis took to social media with a heartfelt plea for funds so she could access specialist treatment abroad, following her seven-year-old son Archie’s muscular dystrophy ...

Health Secretary Neil Gray has been furiously condemned for failing to ensure access to a new muscular dystrophy drug for desperate children. About 30 boys with a rare form of the killer disease ...

When the 90 minutes was up, Messi's goal could not save his team from the lopsided 4-1 defeat that went down as the worst scoreline of any game he has played since joining the club in July 2023.

Already riding their worst start in club history ... but has never been in worse form than he is with the LA Galaxy in 2025 / Bailey Holiver-Imagn Images Vanney and Galaxy General Manager Will ...

Duchenne muscular dystrophy (DMD), recognised by the World Health Organization (WHO) as a rare disease, is the most common form of childhood muscular dystrophy. It is a progressive genetic ...

Even the most optimistic Dragons fan must have feared the worst. But reaching for the record books proved premature as they held out until just four minutes before half-time. They had Stormers ...

It’s Trump’s “worst idea since tariffs,” the Rupert Murdoch-owned newspaper warned with its headline. Trump’s market-spooking trade policies have been relentlessly attacked by the paper, leading to ...

For more than 25 years, Victor has studied DMD and a less aggressive but debilitating variant called Becker muscular dystrophy. This form of muscular dystrophy, usually diagnosed in early adulthood, ...

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 ...