For people with paralysis caused by neurologic injury or disease—such as ALS (also known as Lou Gehrig's disease), stroke, or spinal cord injury—brain-computer interfaces (BCIs) have the potential to restore communication, ...
Jan 13, 2023
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A perplexing range of neurodegenerative diseases are known to attack distinct regions of the brain, causing severe cognitive and motor deficit. The combined impact of these (generally fatal) diseases has inflicted a devastating ...
Dec 21, 2022
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Researchers have made early progress toward a new approach to treating the deadly brain disease amyotrophic lateral sclerosis (ALS): using patients' own immune system T cells.
Oct 21, 2022
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Researchers at the USF Health Morsani College of Medicine, located at the University of South Florida, successfully tested a protein that has the potential to aid in the development of a protein-based therapy for patients ...
Oct 4, 2022
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Neurodegenerative diseases—like amyotrophic lateral sclerosis (ALS, or Lou Gehrig's disease), Alzheimer's, and Parkinson's—are complicated, chronic ailments that can present with a variety of symptoms, worsen at different ...
Sep 27, 2022
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Amyotrophic lateral sclerosis (ALS), also known as Lou Gehrig's disease, is the most common form of motor neuron disease. People with ALS progressively lose the ability to initiate and control muscle movements, including ...
May 27, 2022
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Advocacy groups are pressing U.S. federal regulators to fast-track approval of an experimental drug treatment for the deadly neurological disease ALS (amyotrophic lateral sclerosis), with a decision expected this week.
Mar 28, 2022
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Unable to move a single muscle, even to open your eyes. Completely locked into your own body, yet fully conscious and aware.
Mar 22, 2022
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Researchers at the University of Illinois Chicago are looking at the possibility that gastroenterological changes could be an early warning sign for Lou Gehrig's disease. Their research in animal models also shows a promising ...
Mar 18, 2022
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Using an experimental drug, researchers have been able to suppress a mutated amyotrophic lateral sclerosis (ALS) gene. Studies in mice demonstrate that the therapy could show promise in treating rare, aggressive forms of ...
Jan 24, 2022
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