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Movement Disorders : Official Journal of the Movement Disorder Society|April 9, 2026
Early and Progressive Spinal Cord Atrophy in Spinocerebellar Ataxia Type 1Colette J M Reniers, Teije H van Prooije, Kirsten C J Kapteijns, et al.The Lancet. Neurology|November 15, 2016
Progression characteristics of the European Friedreich's Ataxia Consortium for Translational Studies (EFACTS): a 2 year cohort studyKathrin Reetz, Imis Dogan, Ralf-Dieter Hilgers, et al.Movement Disorders : Official Journal of the Movement Disorder Society|September 15, 2017
Design optimization for clinical trials in early-stage manifest Huntington's diseaseChris Frost, Amy Mulick, Rachael I Scahill, et al.Neuroimage. Clinical|March 13, 2018
Cross-sectional and longitudinal voxel-based grey matter asymmetries in Huntington's diseaseLora Minkova, Sarah Gregory, Rachael I Scahill, et al.Movement Disorders : Official Journal of the Movement Disorder Society|April 16, 2016
Nomenclature of genetic movement disorders: Recommendations of the international Parkinson and movement disorder society task forceConnie Marras, Anthony Lang, Bart P van de Warrenburg, et al.Orphanet Journal of Rare Diseases|August 5, 2020
Onset features and time to diagnosis in Friedreich's AtaxiaElisabetta Indelicato, Wolfgang Nachbauer, Andreas Eigentler, et al.Brain : a Journal of Neurology|November 27, 2018
Spastic paraplegia due to SPAST mutations is modified by the underlying mutation and sexLivia Parodi, Silvia Fenu, Mathieu Barbier, et al.Neuroimage. Clinical|November 2, 2013
Evaluation of multi-modal, multi-site neuroimaging measures in Huntington's disease: Baseline results from the PADDINGTON studyNicola Z Hobbs, James H Cole, Ruth E Farmer, et al.Neuropsychologia|November 1, 2015
The impact of occipital lobe cortical thickness on cognitive task performance: An investigation in Huntington's DiseaseEileanoir B Johnson, Elin M Rees, Izelle Labuschagne, et al.Journal of Neurology|October 27, 2020
PolyQ-expanded ataxin-3 protein levels in peripheral blood mononuclear cells correlate with clinical parameters in SCA3: a pilot studyKathrin Gonsior, Gabriele Anna Kaucher, Patrik Pelz, et al.Pageof 33