These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

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.
    ; . PubMed ID:
    [No 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.
    ; . PubMed ID:
    [No 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]

    Page: [Next] [New Search]
    of 11.