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Movement Disorders : Official Journal of the Movement Disorder Society|November 1, 1996
Intrafamilial variability in Machado-Joseph diseaseS H Subramony, R D CurrierNeurology|September 1, 1986
"Orthostatic tremor' in familial-essential tremorA S Wee, S H Subramony, R D CurrierJournal 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.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.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.Journal of the Neurological Sciences|June 1, 1994
Decreased insulin-like growth factor I-mediated protein tyrosine phosphorylation in human olivopontocerebellar atrophy and lurcher mutant mouseP J Vig, D Desaiah, P Joshi, et al.Zhong Nan Da Xue Xue Bao. Yi Xue Ban = Journal of Central South University. Medical Sciences|July 12, 2011
Clinical challenges in the ataxiasS H SubramonyPageof 16