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They combat tumor growth, but also have a number of undesirable side effects. One of these is severe muscle wasting, known as chemotherapy-induced cachexia. This chronic disease causes ...

The two brothers have Duchenne muscular dystrophy — a rare inherited muscle-wasting disorder that has no cure. "Caleb stopped walking in December of '23, so a little over a year ago. Duncy ...

Three people with spinal muscle atrophy (SMA), a muscle-destroying disease, experienced improved strength and mobility after receiving spinal cord stimulation from an implanted device. Researchers ...

People with spinal muscle atrophy (SMA), an inherited neuromuscular disease, usually experience muscle weakness that impacts movement. New research suggests that electrical spinal cord stimulation ...

Late-stage trial data for Roche’s drug against muscle-wasting Elevidys showed positive results after two years of treatment for male patients aged 4 or older with Duchenne muscular dystrophy.

Yet over the month-long pilot study, “they were getting better and better.” Spinal muscle atrophy or SMA is a genetic disease that gradually destroys motor neurons, nerve cells in the spinal ...

researchers reported what they called the first evidence that a spine-stimulating implant already being tested for paralysis might also aid neurodegenerative diseases like spinal muscle atrophy ...

According to published results, nonoperative treatment yielded similar clinical outcomes at 2 years as operative treatment ...