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Journal Abstract Search

475 related items for PubMed ID: 8068439

  • 1. [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; 46(6):563-71. PubMed ID: 8068439
    [Abstract] [Full Text] [Related]

  • 2. An autopsy case of spinocerebellar ataxia type 6 with mental symptoms of schizophrenia and dementia.
    Tashiro H, Suzuki SO, Hitotsumatsu T, Iwaki T.
    Clin Neuropathol; 1999 Jun; 18(4):198-204. PubMed ID: 10442462
    [Abstract] [Full Text] [Related]

  • 3. [(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
    [Abstract] [Full Text] [Related]

  • 4. [A family with Menzel's disease showing dementia and various extrapyramidal symptoms].
    Iwabuchi K, Nagatomo H, Tanabe T, Oda T, Itoh H, Hanihara T, Yagishita S.
    No To Shinkei; 1993 Sep; 45(9):841-9. PubMed ID: 8217410
    [Abstract] [Full Text] [Related]

  • 5. [An autopsied case of idiopathic late cortical cerebellar atrophy--comparison with other cortical cerebellar atrophy].
    Iwabuchi K, Yagishita S.
    Rinsho Shinkeigaku; 1990 Nov; 30(11):1190-6. PubMed ID: 2085923
    [Abstract] [Full Text] [Related]

  • 6. [Hereditary dentatorubropallidoluysian atrophy--clinical variants in a family and degeneration of cerebral white matter in a proband].
    Miyashita K, Inuzuka T, Ishikawa A, Kondo H, Kawakami A, Takeda S, Ikuta F, Yuasa T.
    No To Shinkei; 1992 Mar; 44(3):279-84. PubMed ID: 1591106
    [Abstract] [Full Text] [Related]

  • 7. [Some problems on the clinical phenotype of Machado-Joseph disease in relation between their ages at onset].
    Iwabuchi K, Kogure T, Oda T, Kato Y, Ohtani K, Endo K, Kosaka K, Amano N, Yagishita S.
    No To Shinkei; 1993 Mar; 45(3):246-54. PubMed ID: 8323819
    [Abstract] [Full Text] [Related]

  • 8. [An autopsy case of hereditary cerebellar atrophy (Holmes-type) with mental symptoms and rhythmic skeletal myoclonus].
    Ohta S, Mizutani Y, Anno M.
    No To Shinkei; 1994 Jul; 46(7):663-70. PubMed ID: 7946622
    [Abstract] [Full Text] [Related]

  • 9. [An autopsied case of type 2 Machado-Joseph's disease or spino-pontine degeneration].
    Iwabuchi K, Nagatomo H, Tanabe T, Sakai H, Yagishita S.
    No To Shinkei; 1993 Aug; 45(8):733-40. PubMed ID: 8217397
    [Abstract] [Full Text] [Related]

  • 10. [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
    [Abstract] [Full Text] [Related]

  • 11. [Autopsy cases of hereditary ataxia pathologically diagnosed as the Japanese type of Joseph disease--cliniconeuropathological findings].
    Kogure T, Oda T, Katoh Y.
    Seishin Shinkeigaku Zasshi; 1990 Oct; 92(3):161-83. PubMed ID: 2353076
    [Abstract] [Full Text] [Related]

  • 12. Primary degeneration of the granular layer of the cerebellum. A study of 14 patients and review of the literature.
    Pascual-Castroviejo I, Gutierrez M, Morales C, Gonzalez-Mediero I, Martínez-Bermejo A, Pascual-Pascual SI.
    Neuropediatrics; 1994 Aug; 25(4):183-90. PubMed ID: 7824090
    [Abstract] [Full Text] [Related]

  • 13. 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
    [Abstract] [Full Text] [Related]

  • 14. [An autopsied case of manifesting chorea, serum antibody to brain proteins, neuronal degeneration in striatum and grumose degeneration in dentate nucleus].
    Ishikawa A, Miyatani N, Yuasa T, Tanaka K, Oyanagi K.
    Rinsho Shinkeigaku; 1990 May; 30(5):510-5. PubMed ID: 2144802
    [Abstract] [Full Text] [Related]

  • 15. [An autopsy case of dentatorubropallidoluysian atrophy showing marked atrophy of the brain stem].
    Morioka E, Nakatsu T, Kuroda S, Yamamoto M, Hosokawa K, Otsuki S.
    No To Shinkei; 1987 Aug; 39(8):769-73. PubMed ID: 2962593
    [Abstract] [Full Text] [Related]

  • 16. [An autopsy case of multiple system atrophy with many Lewy bodies--striatonigral degeneration, olivo-ponto-cerebellar atrophy and autonomic nerve nucleus involvement in the spinal cord].
    Morioka E, Kuroda S, Kuyama K, Otsuki S, Hosokawa K, Namba R.
    No To Shinkei; 1987 Apr; 39(4):361-6. PubMed ID: 3036191
    [Abstract] [Full Text] [Related]

  • 17. [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 Apr; 43(1-2):16-9. PubMed ID: 12820545
    [Abstract] [Full Text] [Related]

  • 18. [Study on argyrophilic inclusions of multisystem atrophy (Oppenheimer)].
    Iwabuchi K, Kosaka K, Haga C, Tuchiya K, Amano N, Itoh K, Yagishita S, Mizutani Y.
    No To Shinkei; 1991 Jun; 43(6):561-8. PubMed ID: 1654964
    [Abstract] [Full Text] [Related]

  • 19. Autosomal-dominant dentatorubropallidoluysian atrophy in the United Kingdom.
    Warner TT, Lennox GG, Janota I, Harding AE.
    Mov Disord; 1994 May; 9(3):289-96. PubMed ID: 8041369
    [Abstract] [Full Text] [Related]

  • 20. [An autopsy case of dentatorubropallidoluysian atrophy (DRPLA) clinically diagnosed as Huntington's chorea].
    Nakano T, Iwabuchi K, Yagishita S, Amano N, Akagi M, Yamamoto Y.
    No To Shinkei; 1985 Aug; 37(8):767-74. PubMed ID: 2934081
    [Abstract] [Full Text] [Related]

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