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Brain and Language|November 7, 2008
Developmental dyslexia and widespread activation across the cerebellar hemispheresHanne Baillieux, Everhard J M Vandervliet, Mario Manto, et al.Scientific Reports|August 1, 2025
Temporal prediction and feedforward control in cerebellar ataxia during spontaneous, instructed, and adaptive auditory-motor coupling while walkingLousin Moumdjian, Bart Moens, Mario Manto, et al.Neurology|April 11, 2014
Autosomal recessive cerebellar ataxia of adult onset due to STUB1 mutationsChantal Depondt, Simona Donatello, Nicolas Simonis, et al.Orphanet Journal of Rare Diseases|March 19, 2021
Research priorities for rare neurological diseases: a representative view of patient representatives and healthcare professionals from the European Reference Network for Rare Neurological DiseasesAnnemarie E M Post, Thomas Klockgether, G Bernhard Landwehrmeyer, et al.Epilepsy Research|September 12, 2013
A new locus for familial temporal lobe epilepsy on chromosome 3qLyne Chahine, Bassel Abou-Khalil, Auli Siren, et al.Cerebellum (London, England)|April 25, 2020
Diagnostic Criteria for Primary Autoimmune Cerebellar Ataxia-Guidelines from an International Task Force on Immune-Mediated Cerebellar AtaxiasMarios Hadjivassiliou, Francesc Graus, Jerome Honnorat, et al.Social Cognitive and Affective Neuroscience|May 1, 2019
The role of the cerebellum in reconstructing social action sequences: a pilot studyFrank Van Overwalle, Sarah De Coninck, Elien Heleven, et al.Brain and Language|September 17, 2017
Cerebellar induced differential polyglot aphasia: A neurolinguistic and fMRI studyPeter Mariën, Kim van Dun, Johanna Van Dormael, et al.Human Molecular Genetics|June 30, 2007
Down-regulation of the dopamine receptor D2 in mice lacking ataxin 1Robert Goold, Michael Hubank, Abigail Hunt, et al.Journal of the Neurological Sciences|March 22, 2017
HLA genotype as a marker of multiple sclerosis prognosis: A pilot studyAndreas P Lysandropoulos, Nicolas Mavroudakis, Massimo Pandolfo, et al.Pageof 35