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Movement Disorders : Official Journal of the Movement Disorder Society|December 19, 2001
Sequence variation in GAA repeat expansions may cause differential phenotype display in Friedreich's ataxiaD O McDaniel, B Keats, V V Vedanarayanan, et al.Journal of the Neurological Sciences|July 1, 1992
Inositol 1,4,5-trisphosphate metabolism in the cerebella of Lurcher mutant mice and patients with olivopontocerebellar atrophyP J Vig, S H Subramony, R D Currier, et al.Brain Research|June 21, 1991
Inositol 1,4,5-trisphosphate receptors and protein kinase C in olivopontocerebellar atrophyD Desaiah, P J Vig, S H Subramony, et al.Human Molecular Genetics|August 15, 2013
Selective inhibition of caspases in skeletal muscle reverses the apoptotic synaptic degeneration in slow-channel myasthenic syndromeHaipeng Zhu, Peter Pytel, Christopher M GomezPediatric Neurology|July 1, 1990
Mistaken diagnoses in continuous muscle fiber activity of peripheral nerve originS H Subramony, C C Parker, O B Evans, et al.Movement Disorders : Official Journal of the Movement Disorder Society|March 1, 1996
Dominantly inherited cerebello-olivary atrophy is not due to a mutation at the spinocerebellar ataxia-I, Machado-Joseph disease, or Dentato-Rubro-Pallido-Luysian atrophy locusS H Subramony, J D Fratkin, B V Manyam, et al.Journal of Neuroscience Research|May 26, 2007
Differential effects of polyglutamine proteins on nuclear organization and artificial reporter splicingJune Sun, Hongzhi Xu, Sandeep Negi, et al.Cerebellum (London, England)|November 29, 2017
Correction to: SPG7 and Impaired Emotional CommunicationLinwei Zhang, Karen N McFarland, S H Subramony, et al.Neurology. Genetics|February 12, 2020
Psychometric properties of the Friedreich Ataxia Rating ScaleChristian Rummey, Louise A Corben, Martin B Delatycki, et al.Neurology|January 14, 2004
Antigliadin antibodies in Huntington's diseaseKhalafalla O Bushara, Martha Nance, Christopher M GomezPageof 23