Despite modern high-throughput sequencing, the genetic cause of most rare movement disorders remains unclear. A research team in Bochum and Tübingen has now solved one piece of the puzzle: The ...
A new mechanism that worsens the symptoms of cerebellar ataxia, a rare degenerative cerebellar disease, has been identified.
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Understanding ataxia from genes to daily life
Ataxia is more than just clumsiness—it’s a neurological condition that affects coordination, balance, speech, and even vision ...
CHICAGO (WLS) -- The Friedrich's Ataxia Research Alliance (FARA) invites families, cyclists, and everyone else to their 5th Annual rideATAXIA Chicago event on July 24, 2016. The multi-route cycling ...
Please provide your email address to receive an email when new articles are posted on . Areas of the brain in those with stroke were analyzed for lesion activity and functional connectivity. In 54% of ...
Solid Biosciences' SGT-212, dual-route gene therapy for Friedreich’s ataxia, receives FDA Fast Track designation for expedited development. Solid Biosciences Inc. has announced that its gene therapy ...
The reality alum, who lives with spinocerebellar ataxia, looked back proudly on the goals she accomplished in 2024 Two years ...
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