Showing results (291-300 of 500) with videos related to

Sort By:
Pageof 50
Movement Disorders : Official Journal of the Movement Disorder Society|February 3, 2011
Quantitative assessment of the evolution of cerebellar signs in spinocerebellar ataxiasEllis Chan, Perrine Charles, Pascale Ribai, et al.
Nature Structural & Molecular Biology|October 13, 2014
Cross-talking noncoding RNAs contribute to cell-specific neurodegeneration in SCA7Jennifer Y Tan, Keith W Vance, Miguel A Varela, et al.
Cell Reports|June 21, 2016
Defects in the CAPN1 Gene Result in Alterations in Cerebellar Development and Cerebellar Ataxia in Mice and HumansYubin Wang, Joshua Hersheson, Dulce Lopez, et al.
Tremor and Other Hyperkinetic Movements (New York, N.Y.)|December 12, 2019
Association of Rare Genetic Variants in Opioid Receptors with Tourette SyndromeChristel Depienne, Sorana Ciura, Oriane Trouillard, et al.
Neuro-Degenerative Diseases|May 31, 2017
SLC25A46 Mutations Associated with Autosomal Recessive Cerebellar Ataxia in North African FamiliesMonia B Hammer, Jinhui Ding, Fanny Mochel, et al.
Neurobiology of Aging|September 21, 2019
A unique common ancestor introduced P301L mutation in MAPT gene in frontotemporal dementia patients from Barcelona (Baix Llobregat, Spain)Leire Palencia-Madrid, Raquel Sánchez-Valle, Ierai Fernández de Retana, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 7, 2007
Construction and validation of a Parkinson's disease mutation genotyping array for the Parkin geneLorraine N Clark, Eneli Haamer, Helen Mejia-Santana, et al.
Brain : a Journal of Neurology|April 2, 2008
Composite cerebellar functional severity score: validation of a quantitative score of cerebellar impairmentSophie Tezenas du Montcel, Perrine Charles, Pascale Ribai, et al.
Tremor and Other Hyperkinetic Movements (New York, N.Y.)|July 17, 2023
Correction: Association of Rare Genetic Variants in Opioid Receptors with Tourette SyndromeChristel Depienne, Sorana Ciura, Oriane Trouillard, et al.
Plos Biology|July 9, 2010
A genome-scale DNA repair RNAi screen identifies SPG48 as a novel gene associated with hereditary spastic paraplegiaMikołaj Słabicki, Mirko Theis, Dragomir B Krastev, et al.
Pageof 50