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Neurology. Genetics|November 22, 2019
A family with spinocerebellar ataxia and retinitis pigmentosa attributed to an <i>ELOVL4</i> mutationChangrui Xiao, Elaine M Binkley, Jessica Rexach, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 24, 2010
Neurochemical alterations in spinocerebellar ataxia type 1 and their correlations with clinical statusGülin Oz, Diane Hutter, Ivan Tkác, et al.
Biological Psychiatry Global Open Science|November 3, 2022
Sensory Over-responsivity and Aberrant Plasticity in Cerebellar Cortex in a Mouse Model of Syndromic AutismDana H Simmons, Silas E Busch, Heather K Titley, et al.
Cerebellum (London, England)|July 10, 2023
Intermuscular Coherence in Spinocerebellar Ataxias 3 and 6: a Preliminary StudyNaoum P Issa, Serdar Aydin, Shail Bhatnagar, et al.
Annals of Neurology|March 26, 2018
Neurochemical abnormalities in premanifest and early spinocerebellar ataxiasJames M Joers, Dinesh K Deelchand, Tianmeng Lyu, et al.
IEEE Transactions on Bio-Medical Engineering|November 12, 2020
Inertial Sensor Algorithms to Characterize Turning in Neurological Patients With Turn HesitationsVrutangkumar V Shah, Carolin Curtze, Martina Mancini, et al.
Biorxiv : the Preprint Server for Biology|December 31, 2025
An Interactive Brain Atlas of KnowledgeLeon Stefanovski, Konstantin Bülau, Leon Martin, et al.
Cerebellum (London, England)|January 13, 2024
Early-Life Social Determinants of SCA6 Age at Onset, Severity, and ProgressionTiffany X Chen, Hannah L Casey, Chi-Ying R Lin, et al.
Movement Disorders Clinical Practice|January 29, 2025
Longitudinal Changes in Patient- and Clinical-Reported Outcomes in Early Spinocerebellar Ataxia Types 1, 2, 3, and 6 from the IDEA StudyAndreea M Rawlings, Rosalind S Chuang, Jeremy D Schmahmann, et al.
The Journal of Clinical Investigation|September 15, 2007
Calpain activation impairs neuromuscular transmission in a mouse model of the slow-channel myasthenic syndromeJason S Groshong, Melissa J Spencer, Bula J Bhattacharyya, et al.
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