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Parkinsonism & Related Disorders|December 9, 2015
Depression and clinical progression in spinocerebellar ataxiasRaymond Y Lo, Karla P Figueroa, Stefan M Pulst, et al.Cerebellum (London, England)|November 17, 2016
The Initial Symptom and Motor Progression in Spinocerebellar AtaxiasLan Luo, Jie Wang, Raymond Y Lo, et al.Tremor and Other Hyperkinetic Movements (New York, N.Y.)|October 24, 2017
Postural Tremor and Ataxia Progression in Spinocerebellar AtaxiasShi-Rui Gan, Jie Wang, Karla P Figueroa, et al.Parkinsonism & Related Disorders|February 28, 2020
The impact of ethnicity on the clinical presentations of spinocerebellar ataxia type 3Shi-Rui Gan, Karla P Figueroa, Hao-Ling Xu, et al.Frontiers in Molecular Biosciences|September 22, 2022
A non-synonymous single nucleotide polymorphism in <i>SIRT6</i> predicts neurological severity in Friedreich ataxiaLayne N Rodden, Christian Rummey, Yi Na Dong, et al.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.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.Pageof 4