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Movement Disorders : Official Journal of the Movement Disorder Society|September 2, 2008
Early symptoms in spinocerebellar ataxia type 1, 2, 3, and 6Christoph Globas, Sophie Tezenas du Montcel, Laslo Baliko, et al.Movement Disorders Clinical Practice|October 27, 2018
Standardized Assessment of Hereditary Ataxia Patients in Clinical StudiesBrigitte K Paap, Sandra Roeske, Alexandra Durr, 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.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.Brain : a Journal of Neurology|February 27, 2018
Mechanistic basis of an epistatic interaction reducing age at onset in hereditary spastic paraplegiaTimothy Newton, Rachel Allison, James R Edgar, 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.Journal of Neurology|June 16, 2026
Cerebellar cognitive-affective syndrome in Friedreich AtaxiaEmilien Petit, Sabrina Sayah, Elisabetta Indelicato, 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.Brain : a Journal of Neurology|January 4, 2022
Clinical and genetic spectra of 1550 index patients with hereditary spastic paraplegiaJean-Loup Méreaux, Guillaume Banneau, Mélanie Papin, et al.Pageof 33