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Scientists present current evidence for a new gene therapy for Duchenne muscular dystrophy called delandistrogene moxeparvovec.
The Associated Press on MSN16d
Chilean woman with muscular dystrophy becomes face of euthanasia debate as bill stalls in SenateWhile right-wing populism surges in some of the world’s leading democracies, Chile’s leftist government is rushing in the opposite direction, taking on sensitive, liberal social issues in its waning ...
The PhD student, who is studying behavioural science at Warwick University, will start the Bidwells Oxford 10k. The race is ...
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 ...
The approval allows the DMD gene therapy to be sold in Japan for up to seven years, but more trials will be needed for full ...
Researchers confirm and explore the role of estrogen-related receptors in regulating energy production in muscle cells during exercise. The findings indicate that developing a drug to boost ...
When she was 8 years old, Moreira was diagnosed with shoulder-girdle muscular dystrophy, a progressive genetic disease that affects all her muscles and causes difficulty breathing, swallowing and ...
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