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Acta Neuropathologica|December 6, 2008
A patient with Huntington's disease and long-surviving fetal neural transplants that developed mass lesionsC Dirk Keene, Rubens C Chang, James B Leverenz, et al.Cerebellum (London, England)|May 6, 2024
Development and Validation of SCACOMS, a Composite Scale for Assessing Disease Progression and Treatment Effects in Spinocerebellar AtaxiaGilbert L'Italien, Evan Popoff, Basia Rogula, et al.Human Molecular Genetics|May 24, 2018
Peripheral blood gene expression reveals an inflammatory transcriptomic signature in Friedreich's ataxia patientsDaniel Nachun, Fuying Gao, Charles Isaacs, et al.Annals of Clinical and Translational Neurology|September 15, 2017
Impact of diabetes in the Friedreich ataxia clinical outcome measures studyAshley McCormick, Jennifer Farmer, Susan Perlman, et al.Movement Disorders : Official Journal of the Movement Disorder Society|January 31, 2012
Mutations in rare ataxia genes are uncommon causes of sporadic cerebellar ataxiaBrent L Fogel, Ji Yong Lee, Jessica Lane, et al.Neurology. Genetics|August 2, 2018
Longitudinal analysis of contrast acuity in Friedreich ataxiaAli G Hamedani, Lauren A Hauser, Susan Perlman, et al.Neurology|December 1, 2022
Efficacy and Safety of N-Acetyl-l-Leucine in Children and Adults With GM2 GangliosidosesKyriakos Martakis, Jens Claassen, Jordi Gascon-Bayari, et al.Movement Disorders : Official Journal of the Movement Disorder Society|June 3, 2026
Frequency of ZFHX3-Mediated Spinocerebellar Ataxia 4 in a US Undiagnosed Ataxia CohortAnnie Chen, Udbhav Avadhani, Kathie Ngo, et al.Journal of the Neurological Sciences|June 24, 2008
Health related quality of life measures in Friedreich AtaxiaElizabeth Epstein, Jennifer M Farmer, Amy Tsou, et al.Journal of Neurology|December 3, 2022
Double blind trial of a deuterated form of linoleic acid (RT001) in Friedreich ataxiaDavid R Lynch, Katherine D Mathews, Susan Perlman, et al.Pageof 10