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Journal Abstract Search


99 related items for PubMed ID: 1424332

  • 21. [(Neurological CPC.55). A 60-year-old woman with progressive cerebellar ataxia, myoclonus, and dementia].
    Morikawa N, Mori H, Sumino S, Kodera M, Shirai T, Kondo T, Mizuno Y.
    No To Shinkei; 1997 Jul; 49(7):663-71. PubMed ID: 9234257
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  • 22. [A family of spino-cerebellar degeneration with disturbance of ocular movement, choreoathetosis, amyotrophy and dementia--a consideration in clinical features].
    Usui S, Beppu H, Hirose K, Tanabe H, Tsubaki T.
    No To Shinkei; 1988 Oct; 40(10):953-61. PubMed ID: 3196499
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  • 23. Distribution of cerebello-olivary degeneration in idiopathic late cortical cerebellar atrophy: clinicopathological study of four autopsy cases.
    Ota S, Tsuchiya K, Anno M, Niizato K, Akiyama H.
    Neuropathology; 2008 Feb; 28(1):43-50. PubMed ID: 18181834
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  • 24. Cerebellar degeneration in hereditary dentatorubral-pallidoluysian atrophy and Machado-Joseph disease.
    Kumada S, Hayashi M, Mizuguchi M, Nakano I, Morimatsu Y, Oda M.
    Acta Neuropathol; 2000 Jan; 99(1):48-54. PubMed ID: 10651027
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  • 25. Vestibular evoked myogenic potentials in patients with spinocerebellar degeneration.
    Takegoshi H, Murofushi T.
    Acta Otolaryngol; 2000 Oct; 120(7):821-4. PubMed ID: 11132714
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  • 26. Human eye fields in the frontal lobe as studied by epicortical recording of movement-related cortical potentials.
    Yamamoto J, Ikeda A, Satow T, Matsuhashi M, Baba K, Yamane F, Miyamoto S, Mihara T, Hori T, Taki W, Hashimoto N, Shibasaki H.
    Brain; 2004 Apr; 127(Pt 4):873-87. PubMed ID: 14960503
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  • 27. [A family with dentato-rubro-pallido-luysian atrophy (DRPLA): an intergenerational contraction of the CAG repeat].
    Murata K, Matsumura R, Nakamuro T, Ichikawa S, Takayanagi T.
    Rinsho Shinkeigaku; 1997 Feb; 37(2):127-30. PubMed ID: 9164145
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  • 32. [Clinical features of "multiple system atrophies"--olivo-ponto-cerebellar atrophy, striato-nigral degeneration and Shy-Drager syndrome].
    Hirayama K, Kita K.
    Rinsho Shinkeigaku; 1985 Oct; 25(10):1196-203. PubMed ID: 4092395
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  • 34. Impaired P50 sensory gating in Machado-Joseph disease.
    Ghisolfi ES, Maegawa GH, Becker J, Zanardo AP, Strimitzer IM, Prokopiuk AS, Pereira ML, Carvalho T, Jardim LB, Lara DR.
    Clin Neurophysiol; 2004 Oct; 115(10):2231-5. PubMed ID: 15351363
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  • 40. 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 locus.
    Subramony SH, Fratkin JD, Manyam BV, Currier RD.
    Mov Disord; 1996 Mar; 11(2):174-80. PubMed ID: 8684388
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