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Neuron|December 11, 2012
Critical roles for anterior insula and dorsal striatum in punishment-based avoidance learningStefano Palminteri, Damian Justo, Céline Jauffret, et al.
European Journal of Human Genetics : EJHG|December 10, 2020
Informing about genetic risk in families with Huntington disease: comparison of attitudes across two decadesLucie Pierron, Juliette Hennessy, Sophie Tezenas du Montcel, et al.
Scientific Reports|November 7, 2022
Forecasting individual progression trajectories in Huntington disease enables more powered clinical trialsIgor Koval, Thomas Dighiero-Brecht, Allan J Tobin, et al.
Neurology. Genetics|January 18, 2024
<i>IRF2BPL</i> Causes Mild Intellectual Disability Followed by Late-Onset AtaxiaSolveig Heide, Claire-Sophie Davoine, Paulina Cunha, et al.
Journal of Neurology|November 17, 2015
Deep brain stimulation of the internal pallidum in Huntington's disease patients: clinical outcome and neuronal firing patternsCécile Delorme, Alister Rogers, Brian Lau, et al.
Neurology|February 27, 2015
Quantifiable evaluation of cerebellar signs in childrenAntoine Filipovic Pierucci, Caterina Mariotti, Marta Panzeri, et al.
Briefings in Bioinformatics|November 7, 2017
A strategy for multimodal data integration: application to biomarkers identification in spinocerebellar ataxiaImene Garali, Isaac M Adanyeguh, Farid Ichou, et al.
Annals of Clinical and Translational Neurology|March 10, 2015
Survival and severity in dominant cerebellar ataxiasMarie-Lorraine Monin, Sophie Tezenas du Montcel, Cecilia Marelli, et al.
European Journal of Neurology|January 6, 2025
Substantia nigra degeneration in spinocerebellar ataxia 2 and 7 using neuromelanin-sensitive imagingLydia Chougar, Giulia Coarelli, François-Xavier Lejeune, et al.
Archives of Neurology|August 20, 2003
Prevalence of dentatorubral-pallidoluysian atrophy in a large series of white patients with cerebellar ataxiaIsabelle Le Ber, Agnès Camuzat, Giovanni Castelnovo, et al.
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