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Annals of Neurology|February 26, 2005
Spinocerebellar ataxia type 26 maps to chromosome 19p13.3 adjacent to SCA6Guo-Yun Yu, Michael J Howell, Matthew J Roller, et al.
Biology Open|December 17, 2016
Polyglutamine length-dependent toxicity from α1ACT in Drosophila models of spinocerebellar ataxia type 6Wei-Ling Tsou, Sultan H Qiblawi, Ryan R Hosking, et al.
Alzheimer'S & Dementia (New York, N. Y.)|May 23, 2022
Brain simulation augments machine-learning-based classification of dementiaPaul Triebkorn, Leon Stefanovski, Kiret Dhindsa, et al.
Neurobiology of Disease|July 4, 2006
Activation of apoptotic pathways at muscle fiber synapses is circumscribed and reversible in a slow-channel syndrome modelBhupinder P S Vohra, Jason S Groshong, Roberto Zayas, et al.
Frontiers in Neuroinformatics|December 5, 2015
TVB-EduPack-An Interactive Learning and Scripting Platform for The Virtual BrainHenrik Matzke, Michael Schirner, Daniel Vollbrecht, et al.
Neuro-Ophthalmology (Aeolus Press)|August 26, 2011
Retinal Nerve Fibre Layer and Macular Thinning in Spinocerebellar Ataxia and Cerebellar Multisystem AtrophyJohn H Pula, Vernon L Towle, Victoria M Staszak, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|August 2, 2002
Active calcium accumulation underlies severe weakness in a panel of mice with slow-channel syndromeChristopher M Gomez, Ricardo A Maselli, Jason Groshong, et al.
Archives of Neurology|December 10, 2002
Spinocerebellar ataxia in monozygotic twinsJohn H Anderson, Peka S Christova, Ting-dong Xie, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|April 19, 2013
WDR81 is necessary for purkinje and photoreceptor cell survivalMaria Traka, Kathleen J Millen, Devon Collins, et al.
Neurology|February 16, 2026
Pearls & Oy-sters: SCA27B as an Elusive Genetic Cause of Episodic Neurologic Symptoms in Later AdulthoodJacob Yomtoob, Lucy Morse, Ignacio Juan Keller Sarmiento, et al.
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