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Annals of Neurology|July 1, 1995
Molecular and clinical correlations in spinocerebellar ataxia type 3 and Machado-Joseph diseaseT Matilla, A McCall, S H Subramony, et al.Movement Disorders : Official Journal of the Movement Disorder Society|January 12, 2010
Measuring the rate of progression in Friedreich ataxia: implications for clinical trial designLisa S Friedman, Jennifer M Farmer, Susan Perlman, et al.Brain Connectivity|May 25, 2021
Genotypic Differences in Networks Supporting Regional Predictors of Speech Rate in Spinocerebellar Ataxia: Preliminary ObservationsJohn J Sidtis, Christopher M GomezJournal of Neurology, Neurosurgery, and Psychiatry|August 20, 2014
The autosomal dominant spinocerebellar ataxias: emerging mechanistic themes suggest pervasive Purkinje cell vulnerabilityKatherine E Hekman, Christopher M GomezNeurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|March 31, 2007
Molecular pathogenesis of spinocerebellar ataxia type 6Holly B Kordasiewicz, Christopher M GomezPediatric Neurology|November 1, 1995
Treatment of childhood dermatomyositis with high dose intravenous immunoglobulinV Vedanarayanan, S H Subramony, L I Ray, et al.Research Communications in Molecular Pathology and Pharmacology|October 6, 1999
The effects of calbindin D-28K and parvalbumin antisense oligonucleotides on the survival of cultured Purkinje cellsP J Vig, D O McDaniel, S H Subramony, et al.The American Journal of the Medical Sciences|May 1, 1992
Case report: autonomic postganglionic denervation--sural nerve and saphenous vein biopsyM Montani, S H Subramony, H G Langford, et al.Research Communications in Molecular Pathology and Pharmacology|September 1, 1995
Developmental changes in cerebellar endothelin-1 receptors in the neurologic mouse lurcher mutantP J Vig, D Desaiah, S H Subramony, et al.European Neurology|January 1, 1986
Systemic lupus erythematosus presenting with recurrent acute demyelinating polyneuropathyT J Millette, S H Subramony, A S Wee, et al.Pageof 23