Last Updated: 09/26/2026
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Found 55 publications
Beyond neuronal degeneration: oligodendroglial dysfunction as a driver of spinocerebellar ataxia type 1 pathogenesis.
Journal: The Journal of clinical investigation
Published: June 15, 2026
Correction: The Natural History Study and Biomarker Collection of the Clinical Research Consortium for the Study of Cerebellar Ataxia (CRC-SCA).
Journal: Cerebellum (London, England)
Published: November 11, 2025
The Natural History Study and Biomarker Collection of the Clinical Research Consortium for the Study of Cerebellar Ataxia (CRC-SCA).
Journal: Cerebellum (London, England)
Published: July 03, 2025
Suicidal Ideation in Spinocerebellar Ataxia.
Journal: The Journal of neuropsychiatry and clinical neurosciences
Published: May 12, 2025
Mutations in the cytoplasmic iron-sulfur assembly protein CIAO1 cause neuromuscular deficits.
Journal: The Journal of clinical investigation
Published: March 06, 2025
Bridging the gap: insights into sensorimotor deficits in NMDA receptor antibody encephalitis.
Journal: The Journal of clinical investigation
Published: March 03, 2025
Spinocerebellar Ataxia Progression Measured with the Patient-Reported Outcome Measure of Ataxia.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: November 15, 2024
Gigaxonin, mutated in Giant Axonal Neuropathy, interacts with TDP-43 and other RNA binding proteins.
Gigaxonin, mutated in Giant Axonal Neuropathy, interacts with TDP-43 and other RNA binding proteins.
Journal: bioRxiv : the preprint server for biology
Published: September 16, 2024
Last Updated: 09/26/2026