Researchers at Kumamoto University have demonstrated that iron supplementation can significantly alleviate muscle pathology and functional decline in a mouse model of facioscapulohumeral muscular ...
According to new research from the University of Delaware, nearly 40% of American adults ages 18 to 64 with arthritis—almost ...
With a progressive disease like FSHD, the loss of abilities and independence has an unpredictable timeline, says columnist.
Assistive Technology Development, or ATDev, is working with people with disabilities to develop systems for rehab and daily ...
Indiana residents with muscular dystrophy can apply for a free accessible van through the Muscular Dystrophy Family Foundation's annual giveaway program. The foundation awards accessible vans to one ...
NEW YORK – The US Food and Drug Administration has granted GenEditBio permission to launch a Phase I/II trial to evaluate GEB-101, a gene-editing therapy for TGFBI-associated corneal dystrophy, the ...
Waking up, hopping out of the bed, and stumbling to the kitchen for a cup of coffee: It’s an everyday routine most people don’t think twice about. But for children with spinal muscular atrophy, simply ...
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Abu Dhabi leads world in breakthrough gene replacement therapy 'ITVISMA' for spinal muscular atrophy
ABU DHABI, 28th December, 2025 (WAM) -- Abu Dhabi marks landmark achievement in becoming the first in the world to deliver ITVISMA (onasemnogene abeparvovec) for the treatment of spinal muscular ...
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