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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.
EMBO Molecular Medicine|October 11, 2021
CCG•CGG interruptions in high-penetrance SCA8 families increase RAN translation and protein toxicityBarbara A Perez, Hannah K Shorrock, Monica Banez-Coronel, 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.
Parkinsonism & Related Disorders|November 2, 2017
Dystonia and ataxia progression in spinocerebellar ataxiasPei-Hsin Kuo, Shi-Rui Gan, Jie Wang, et al.
Orphanet Journal of Rare Diseases|November 15, 2013
Clinical characteristics of patients with spinocerebellar ataxias 1, 2, 3 and 6 in the US; a prospective observational studyTetsuo Ashizawa, Karla P Figueroa, Susan L Perlman, 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.
Annals of Neurology|April 24, 2012
FXN methylation predicts expression and clinical outcome in Friedreich ataxiaMarguerite V Evans-Galea, Nissa Carrodus, Simone M Rowley, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 4, 2025
Spinocerebellar Ataxia Progression Measured with the Patient-Reported Outcome Measure of AtaxiaAnna L Burt, Gilbert L'Italien, Susan L Perlman, et al.
Cerebellum (London, England)|January 2, 2024
The Cerebellar Cognitive Affective/Schmahmann Syndrome Scale in Spinocerebellar AtaxiasLouisa P Selvadurai, Susan L Perlman, Tetsuo Ashizawa, et al.
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