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Journal Abstract Search

213 related items for PubMed ID: 8297664

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. [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]

  • 3. [Linkage study of hereditary spinocerebellar ataxia, and probable correlation for the loci to the disease phenotypes].
    Sasaki H.
    Rinsho Shinkeigaku; 1993 Dec; 33(12):1285-7. PubMed ID: 8174326
    [Abstract] [Full Text] [Related]

  • 4. [Spinocerebellar ataxia 1--clinical study of 17 patients in a large pedigree].
    Sasaki H, Wakisaka A, Koyama T, Hamada T, Shima K, Tashiro K, Hashimoto K, Miyagishi T.
    No To Shinkei; 1993 Jun; 45(6):502-8. PubMed ID: 8363844
    [Abstract] [Full Text] [Related]

  • 5. Machado-Joseph disease: an autosomal dominant motor system degeneration.
    Rosenberg RN.
    Mov Disord; 1992 Jun; 7(3):193-203. PubMed ID: 1620135
    [Abstract] [Full Text] [Related]

  • 6. [A clinical study of a family affected with HLA-linked hereditary spinocerebellar ataxia].
    Sasaki H, Hamada T, Wakisaka A, Tashiro K.
    No To Shinkei; 1990 Nov; 42(11):1103-11. PubMed ID: 2076357
    [Abstract] [Full Text] [Related]

  • 7. Structural and immunocytochemical features of olivopontocerebellar atrophy caused by the spinocerebellar ataxia type 1 (SCA-1) mutation define a unique phenotype.
    Robitaille Y, Schut L, Kish SJ.
    Acta Neuropathol; 1995 Nov; 90(6):572-81. PubMed ID: 8615077
    [Abstract] [Full Text] [Related]

  • 8. [Siblings with spinocerebellar ataxia type 1 (SCA 1)--diagnosis by detecting the expansion of CAG repeat on chromosome 6p].
    Hanihara T, Takahashi T, Inoue K, Yamada Y, Iwabuchi K.
    Rinsho Shinkeigaku; 1994 May; 34(5):508-10. PubMed ID: 7924069
    [Abstract] [Full Text] [Related]

  • 9. [Clinical study of gene locus heterogeneity in hereditary olivopontocerebellar atrophy (OPCA)--report of 2 pedigrees affected with non SCA1 type OPCA].
    Sasaki H, Wakisaka A, Tashiro K, Hamada T, Shima K.
    Rinsho Shinkeigaku; 1991 Nov; 31(11):1170-6. PubMed ID: 1813183
    [Abstract] [Full Text] [Related]

  • 10. [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 Nov; 92(3):161-83. PubMed ID: 2353076
    [Abstract] [Full Text] [Related]

  • 11. Brain acetylcholinesterase activity is markedly reduced in dominantly-inherited olivopontocerebellar atrophy.
    Kish SJ, Schut L, Simmons J, Gilbert J, Chang LJ, Rebbetoy M.
    J Neurol Neurosurg Psychiatry; 1988 Apr; 51(4):544-8. PubMed ID: 3164041
    [Abstract] [Full Text] [Related]

  • 12. Hereditary ataxia.
    Rosenberg RN, Grossman A.
    Neurol Clin; 1989 Feb; 7(1):25-36. PubMed ID: 2564162
    [Abstract] [Full Text] [Related]

  • 13. [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]

  • 14. [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]

  • 15. [Two siblings of familial amyotrophic lateral sclerosis with multisystemic degeneration characterized by mild involvement of the middle root zone of the posterior column, Clarke's nuclei and spinocerebellar tract].
    Yoshida M, Okuda S, Murakami N, Hashizume Y, Sobue G.
    Rinsho Shinkeigaku; 1995 Jun; 35(6):589-99. PubMed ID: 8521632
    [Abstract] [Full Text] [Related]

  • 16. [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]

  • 17. Autosomal dominant spinocerebellar ataxia (SCA) in a Siberian founder population: assignment to the SCA1 locus.
    Lunkes A, Goldfarb LG, Platonov FA, Alexeev VP, Duenas-Barajas E, Gajdusek DC, Auburger G.
    Exp Neurol; 1994 Apr; 126(2):310-2. PubMed ID: 7925830
    [Abstract] [Full Text] [Related]

  • 18. Multiple system atrophy with retinal degeneration in a young child.
    Nishimura M, Mito T, Takashima S, Kawahara H, Tanaka J, Nakamura H, Kisa T.
    Neuropediatrics; 1987 May; 18(2):91-5. PubMed ID: 3474543
    [Abstract] [Full Text] [Related]

  • 19. [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]

  • 20. 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
    [Abstract] [Full Text] [Related]

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