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Research Article

Electronystagmographic Findings in Patients with Cerebral Degenerative Disease

Pages 136-139 | Published online: 08 Jul 2009

References

  • Greenfield JG. The spino-cerebellar degenerations. Ox-ford: Blackwell Scientific, 1954: 27–97.
  • Harding A. The clinical features and classification of the late onset autosomal dominant cerebellar ataxias. A study of 11 families, including descendants of 'the Drew family of Walworth'. Brain 1982; 105: 1–28.
  • David NJ, Mackey EA, Smith JL. Further observa-tions in progressive supranuclear palsy. Neurology 1968; 18: 349–56.
  • Steele JC, Richardson JC, Olszewski J. Progressive supranuclear palsy. A heterogeneous degeneration in-volving the brain stem, basal ganglia and cerebellum with vertical gaze and pseudobulbar palsy, nuchal dys-tonia and dementia. Arch Neurol 1964; 10: 333–59.
  • White OB, Saint-Cyr JA, Sharpe JA. Ocular motor deficits in Parkinson's disease. 1. The horizontal vestibulo-ocular reflex and its regulation. Brain 1983; 106: 555–70.
  • White OB, Saint-Cyr JA, Tomlinson RD, Sharpe JA. Ocular motor deficits in Parkinson's disease. 2. Control of the saccadic and smooth pursuit systems. Brain 1983; 106: 571–87.
  • White OB, Saint-Cyr JA, Tomlinson RD, Sharpe JA. Ocular motor deficits in Parkinson's disease. 3. Coordi-nation of eye and head movements. Brain 1988; 111: 115–29.
  • Gibb WRG, Luthert PJ, Marsden CD. Corticobasal degeneration. Brain 1989; 112: 1171–92.
  • Riley DE, Lang AE, Lewis A, et al. Cortical-basal ganglionic degeneration. Neurology 1990; 40: 1203–12.
  • Stockwell CW. Vestibular function tests. In: Paparella MM, Shumrick DA, Gluckman JL, Meyerhoff WL, eds. Otolaryngology, vol. 2, 3rd edn. Philadelphia, PA: Saunders, 1991: 925–30.
  • Takemori S, Cohen B. Visual suppression of vestibular nystagmus in rhesus monkeys. Brain Res 1974; 72: 203–12.
  • Mancall EL. Late (acquired) cortical cerebellar atro-phy. In: Vinken PJ, Bruyn GW, eds. Handbook of clinical neurology, vol. 21. Amsterdam: Elsevier, 1975: 477.
  • Dejerine J, Andre-Thomas A. L'atrophie olivo-ponto-cerebelleuse. Nouv Iconogr Salpet 1900; 13: 330–70.
  • Graham JG, Oppenheimer DR. Orthostatic hypoten-sion and nicotine sensitivity in a case of multiple sys-tem atrophy. J Neurol Neurosurg Psychiatry 1969; 32: 28–34.
  • Yakura H, Wakisaka A, Fujimoto S, et al. Hereditary ataxia and HL-A genotypes. N Engl J Med 1974; 291: 154–5.
  • Zhuchenko 0, Bailey J, Bonnen P, et al. Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alphalA-voltage-dependent calcium channel. Nature Genet 1997; 15: 62–9.
  • Nakano KK, Dawson DM, Spence A. Machado dis-ease. A hereditary ataxia in Portuguese emigrants to Massachusetts. Neurology 1972; 22: 49–55.
  • Kawaguchi Y, Okamoto T, Taniwaki M, et al. CAG expansion in a novel gene from Machado-Joseph dis-ease at chromosome 14q. Nature Genet 1994; 8: 221–8.
  • Naito H, Oyanagi S. Familial myoclonus epilepsy and choreoathetosis;hereditarydentatorubral-pal-lidoluysian atrophy. Neurology 1982; 32: 798.
  • Koide R, Ikeuchi T, Onodera 0, et al. Unstable expan-sion of CAG repeat in hereditary dentatorubral-pal-lidoluysian atrophy (DRPLA). Nature Genet 1994; 6: 9.
  • Strumpell A. Beitrage zur Pathologie des Rucken-marks. Arch Psychiatr Nervenkr 1880; 10: 676.
  • Harding AE. Friedreich's ataxia: a clinical and genetic study of 90 families with an analysis of early diagnostic criteria and intrafamilial clustering of clinical features. Brain 1981; 104: 589–620.
  • Baloh RW, Konrad HR, Honrubia V. Vestibulo-ocular function in patients with cerebellar atrophy. Neurology 1975; 25: 160–8.
  • Takemori S. Visual suppression of vestibular nystag-mus after cerebellar lesions. Ann Otol 1975; 84: 318–
  • Leigh RJ, Zee DS. The neurology of eye movements, 2nd edn. Philadelphia, PA: F.A. Davis Company, 1991: 393–5.

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