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Journal Abstract Search

129 related items for PubMed ID: 2076357

  • 1. [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
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  • 2. [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
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  • 9. [Extrapyramidal manifestations in hereditary olivopontocerebellar atrophy--clinical study of 10 cases in three affected pedigrees].
    Sasaki H, Wakisaka A, Doi S, Hamada K, Hamada T, Shima K, Tashiro K.
    Hokkaido Igaku Zasshi; 1992 Jan; 67(1):55-66. PubMed ID: 1559661
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  • 10. Spinocerebellar ataxia: variable age of onset and linkage to human leukocyte antigen in a large kindred.
    Zoghbi HY, Pollack MS, Lyons LA, Ferrell RE, Daiger SP, Beaudet AL.
    Ann Neurol; 1988 Jun; 23(6):580-4. PubMed ID: 3165612
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  • 11. Linkage study of dominantly inherited olivo-ponto-cerebellar atrophy (OPCA) and Holmes' ataxia.
    Sasaki H, Wakisaka A, Katoh T, Yoshida MC, Hamada T, Shima K, Matsuura T, Tashiro K.
    Jinrui Idengaku Zasshi; 1988 Dec; 33(4):423-38. PubMed ID: 3251076
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  • 12. Linkage studies in spinocerebellar ataxia (SCA).
    Morton NE, Lalouel JM, Jackson JF, Currier RD, Yee S.
    Am J Med Genet; 1980 Dec; 6(3):251-7. PubMed ID: 7424977
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  • 13. Genetic heterogeneity of dominantly inherited olivopontocerebellar atrophy (OPCA) in the Japanese: linkage study of two pedigrees and evidence for the disease locus on chromosome 12q (SCA2).
    Ihara T, Sasaki H, Wakisaka A, Takada A, Yoshiki T, Matsuura T, Hamada T, Suzuki Y, Tashiro K.
    Jpn J Hum Genet; 1994 Sep; 39(3):305-13. PubMed ID: 7841441
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  • 15. [Clinico-genetic study of type I spinocerebelllar ataxia].
    Svetel M, Culjković B, Sternić N, Dragasević B, Stojković I, Romac S, Kostić VS.
    Srp Arh Celok Lek; 1999 Sep; 127(5-6):157-62. PubMed ID: 10500422
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  • 16. [Multivariate analysis of the clinical signs in late cortical cerebellar atrophy (LCCA) in Japan--compared with olivo-ponto-cerebellar atrophy (OPCA) and hereditary cortical cerebellar atrophy (HCCA)].
    Yanagimoto S, Takayanagi T, Hirayama K, Nakamura R, Yanagisawa N.
    Rinsho Shinkeigaku; 1992 Sep; 32(9):951-5. PubMed ID: 1300266
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