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Neurobiology of Disease|February 7, 2026
Cognitive impairment in SCA3: A multi-center cohort study with demographic, imaging, and biomarker correlatesRoderick P P W M Maas, Hector Garcia-Moreno, Jennifer Faber, et al.Parkinsonism & Related Disorders|November 2, 2017
Dystonia and ataxia progression in spinocerebellar ataxiasPei-Hsin Kuo, Shi-Rui Gan, Jie Wang, et al.Journal of the Neurological Sciences|May 27, 2020
Dysphagia in spinocerebellar ataxias type 1, 2, 3 and 6Chen-Ya Yang, Ruo-Yah Lai, Nadia Amokrane, et al.Journal of Neurosurgery|June 17, 2023
Responsive neurostimulation as a treatment for super-refractory focal status epilepticus: a systematic review and case seriesLia D Ernst, Ahmed M Raslan, Angela Wabulya, et al.Movement Disorders : Official Journal of the Movement Disorder Society|October 29, 2021
Characterization of Lifestyle in Spinocerebellar Ataxia Type 3 and Association with Disease SeverityHolger Hengel, Peter Martus, Jennifer Faber, et al.Movement Disorders : Official Journal of the Movement Disorder Society|July 9, 2022
Differential Temporal Dynamics of Axial and Appendicular Ataxia in SCA3Roderick P P W M Maas, Steven Teerenstra, Manuela Lima, et al.Journal of Neurology|November 3, 2022
The frequency of non-motor symptoms in SCA3 and their association with disease severity and lifestyle factorsHolger Hengel, Peter Martus, Jennifer Faber, 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.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.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.Pageof 5