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Journal Abstract Search

370 related items for PubMed ID: 14673899

  • 1. Pure cerebello-olivary degeneration of Marie, Foix, and Alajouanine presenting with progressive cerebellar ataxia, cognitive decline, and chorea.
    Fox SH, Nieves A, Bergeron C, Lang AE.
    Mov Disord; 2003 Dec; 18(12):1550-4. PubMed ID: 14673899
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  • 2. [Olivopontocerebellar atrophy as an important differential diagnosis in atactic gait disorders in elderly patients].
    Waespe W, Hayek J, Wichmann W, Bader JP.
    Schweiz Med Wochenschr; 1988 Jul 12; 118(27-28):1032-8. PubMed ID: 3166204
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  • 4. 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 12; 11(2):174-80. PubMed ID: 8684388
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  • 5. [Clinical types of spinocerebellar degeneration and evaluation with MR imaging].
    Kojima S.
    Rinsho Shinkeigaku; 1993 Dec 12; 33(12):1294-6. PubMed ID: 8174328
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  • 6. [The tardive cerebellar cortical atrophy of Pierre Marie, Foix and Alajouanine. A clinical case report].
    Trebini F, Appiotti A, Scarzella G.
    Minerva Med; 1990 Apr 12; 81(4):315-7. PubMed ID: 2342656
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  • 8. [Comparison between MRI and 3D-SSP in olivopontocerebellar atrophy and cortical cerebellar atrophy].
    Hamaguchi H, Kanda F, Hosaka K, Fujii M, Chihara K.
    Rinsho Shinkeigaku; 2004 Apr 12; 44(4-5):263-7. PubMed ID: 15287507
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  • 12. Patterns of fractional anisotropy changes in white matter of cerebellar peduncles distinguish spinocerebellar ataxia-1 from multiple system atrophy and other ataxia syndromes.
    Prakash N, Hageman N, Hua X, Toga AW, Perlman SL, Salamon N.
    Neuroimage; 2009 Aug 12; 47 Suppl 2():T72-81. PubMed ID: 19446636
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  • 14. [Man aged 49 years suffering from progressive clinical picture with palatal tremor, segmental myoclonus, ataxia, parkinsonism, amyotrophy, pyramidal signs, supranuclear ophthalmoplegia and cognitive decline].
    Berciano J, Montón FI, Maeso MC, Ferrer I.
    Neurologia; 2002 May 12; 17(5):237-43. PubMed ID: 12031213
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  • 15. [A case of adult-onset Huntington disease presenting with spasticity and cerebellar ataxia, mimicking spinocerebellar degeneration].
    Kageyama Y, Yamamoto S, Ueno M, Ichikawa K.
    Rinsho Shinkeigaku; 2003 May 12; 43(1-2):16-9. PubMed ID: 12820545
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  • 18. Idiopathic very late-onset cerebellar ataxia: a Brazilian case series.
    Teive HA, Moscovich M, Moro A, Farah M, Arruda WO, Munhoz RP.
    Arq Neuropsiquiatr; 2015 Nov 12; 73(11):903-5. PubMed ID: 26517211
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  • 20. [Autosomal recessive hereditary cortical cerebellar atrophy with striatal degeneration--two siblings showing choreoathetoid movement, ataxia, dementia, and amenorrhea].
    Iwabuchi K, Nakazawa Y, Akai J, Yagishita S, Amano N.
    No To Shinkei; 1994 Jun 12; 46(6):563-71. PubMed ID: 8068439
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