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Clinical Interventions in Aging|March 13, 2020
Rapidly Progressing Neurocognitive Disorder in a Male with FXTAS and Alzheimer's DiseaseElber Yuksel Aydin, Andrea Schneider, Dragana Protic, et al.Journal of the Neurological Sciences|July 4, 2025
The clinical burden of Friedreich ataxia in the United States: A retrospective claims database analysisSusan Perlman, Su Zhang, Juliana Setyawan, et al.Neurochemical Research|May 8, 2007
Myelin breakdown and iron changes in Huntington's disease: pathogenesis and treatment implicationsGeorge Bartzokis, Po H Lu, Todd A Tishler, et al.Nature Communications|May 9, 2013
SMRT compounds abrogate cellular phenotypes of ataxia telangiectasia in neural derivatives of patient-specific hiPSCsPeiyee Lee, Nathan T Martin, Kotoka Nakamura, et al.Orphanet Journal of Rare Diseases|July 31, 2016
Nosological delineation of congenital ocular motor apraxia type Cogan: an observational studySarah Wente, Simone Schröder, Johannes Buckard, et al.Plos Genetics|April 29, 2017
Homozygous ARHGEF2 mutation causes intellectual disability and midbrain-hindbrain malformationEthiraj Ravindran, Hao Hu, Scott A Yuzwa, et al.Neurodegenerative Disease Management|July 28, 2018
Double-blind, randomized and controlled trial of EPI-743 in Friedreich's ataxiaTheresa Zesiewicz, Jason L Salemi, Susan Perlman, et al.Neurology and Therapy|May 30, 2024
Video-Based Kinematic Analysis of Movement Quality in a Phase 3 Clinical Trial of Troriluzole in Adults with Spinocerebellar Ataxia: A Post Hoc AnalysisGilbert J L'Italien, Evangelos K Oikonomou, Rohan Khera, et al.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.Pageof 26