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Human Mutation|November 7, 2019
A diagnostic ceiling for exome sequencing in cerebellar ataxia and related neurological disordersKathie J Ngo, Jessica E Rexach, Hane Lee, et al.Brain : a Journal of Neurology|October 28, 2025
Predictive models for ataxia progression and conversion in spinocerebellar ataxia type 1 and 3Emilien Petit, Giulia Coarelli, David Morgan, et al.The Journal of Neuropsychiatry and Clinical Neurosciences|May 12, 2025
Suicidal Ideation in Spinocerebellar AtaxiaLevi Peppel, Ruo-Yah Lai, Christian Rummey, et al.Annals of Neurology|September 12, 2024
Clinical, Radiological and Pathological Features of a Large American Cohort of Spinocerebellar Ataxia (SCA27B)Widad Abou Chaar, Anirudh N Eranki, Hannah A Stevens, et al.Movement Disorders Clinical Practice|February 29, 2024
Fatigue Impacts Quality of Life in People with Spinocerebellar AtaxiasRuo-Yah Lai, Christian Rummey, Christian J Amlang, et al.Cerebellum (London, England)|July 18, 2025
The Natural History Study and Biomarker Collection of the Clinical Research Consortium for the Study of Cerebellar Ataxia (CRC-SCA)Yicheng Lin, Nadia Amokrane, Sandie Worley, et al.Journal of Clinical Medicine|November 19, 2020
Safety and Tolerability of SRX246, a Vasopressin 1a Antagonist, in Irritable Huntington's Disease Patients-A Randomized Phase 2 Clinical TrialMichael J Brownstein, Neal G Simon, Jeffrey D Long, et al.JAMA Neurology|November 17, 2015
Clinical-Genetic Associations in the Prospective Huntington at Risk Observational Study (PHAROS): Implications for Clinical Trials, Kevin Michael Biglan, Ira Shoulson, et al.Pageof 10