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Neurology|July 1, 1996
Decreased parvalbumin immunoreactivity in surviving Purkinje cells of patients with spinocerebellar ataxia-1P J Vig, J D Fratkin, D Desaiah, et al.Muscle & Nerve|October 15, 1998
Lethal neonatal autosomal recessive axonal sensorimotor polyneuropathyV V Vedanarayanan, S Smith, S H Subramony, et al.Journal of Child Neurology|July 25, 2025
Disease Progression in Children With Friedreich Ataxia: Functional Performance and Other Outcome Assessments in the FACHILD StudyChristian Rummey, Susan Perlman, S H Subramony, et al.BMC Neurology|June 14, 2023
Pontine stroke in a patient with Chronic Progressive External Ophthalmoplegia (CPEO): a case reportYazan Eliyan, Kourosh Rezania, Christopher M Gomez, et al.Current Opinion in Ophthalmology|September 3, 2010
Ophthalmologic features of the common spinocerebellar ataxiasJohn H Pula, Christopher M Gomez, Jorge C KattahThe Journal of Neuroscience : the Official Journal of the Society for Neuroscience|April 26, 2013
Skeletal muscle calpain acts through nitric oxide and neural miRNAs to regulate acetylcholine release in motor nerve terminalsHaipeng Zhu, Bula Bhattacharyya, Hong Lin, et al.Neurology|May 10, 2006
Evaluation of sleep and daytime somnolence in spinocerebellar ataxia type 6 (SCA6)Michael J Howell, Mark W Mahowald, Christopher M GomezMuscle & Nerve|July 15, 2011
Confirmation of the severe phenotypic effect of serine at codon 41 of the superoxide dismutase 1 geneS H Subramony, Tetsuo Ashizawa, Leigh Langford, et al.Journal of Molecular Neuroscience : MN|December 11, 2012
Generation of human-induced pluripotent stem cells to model spinocerebellar ataxia type 2 in vitroGuangbin Xia, Katherine Santostefano, Takashi Hamazaki, et al.Journal of Neurology|June 19, 2013
Analysis of the visual system in Friedreich ataxiaLauren A Seyer, Kristin Galetta, James Wilson, et al.Pageof 23