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News from NINDS


Picture of two neurons from a mouse spinal cord.

Silencing a faulty gene may uncover clues to rare forms of ALS

Monday, January 24, 2022

Using an experimental drug, researchers were 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 ALS caused by mutations in the fused in sarcoma (FUS) gene.

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National Advisory Council (NANDSC) Meeting - February 2022

Wednesday, February 2, 2022

The 215th meeting of the National Advisory Neurological Disorders and Stroke Council will be held virtually on February 2-3, 2022. For more information, visit the Advisory Council web page.

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Doctor Walter Koroshetz