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93 related items for PubMed ID: 1628432

  • 1. [Linkage study of hereditary olivopontocerebellar atrophy: genetic evidence for locus heterogeneity in Japanese cases].
    Sasaki H, Wakisaka A, Tashiro K, Hamada T, Shima K.
    Rinsho Shinkeigaku; 1992 Jan; 32(1):17-22. PubMed ID: 1628432
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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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  • 3. [Linkage study of Machado-Joseph disease: genetic evidence for the locus different from SCA1].
    Sasaki H, Wakisaka A, Tashiro K, Hamada T, Katoh T.
    Rinsho Shinkeigaku; 1992 Jan; 32(1):13-6. PubMed ID: 1628431
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  • 4. 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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  • 5. [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
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  • 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
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  • 7. [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
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  • 9. The gene for autosomal dominant spinocerebellar ataxia (SCA1) maps telomeric to the HLA complex and is closely linked to the D6S89 locus in three large kindreds.
    Zoghbi HY, Jodice C, Sandkuijl LA, Kwiatkowski TJ, McCall AE, Huntoon SA, Lulli P, Spadaro M, Litt M, Cann HM.
    Am J Hum Genet; 1991 Jul; 49(1):23-30. PubMed ID: 2063871
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  • 10. Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to chromosome 12q23-24.1.
    Gispert S, Twells R, Orozco G, Brice A, Weber J, Heredero L, Scheufler K, Riley B, Allotey R, Nothers C.
    Nat Genet; 1993 Jul; 4(3):295-9. PubMed ID: 8358438
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  • 11. [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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  • 12. The gene for autosomal dominant spinocerebellar ataxia (SCA1) maps centromeric to D6S89 and shows no recombination, in nine large kindreds, with a dinucleotide repeat at the AM10 locus.
    Kwiatkowski TJ, Orr HT, Banfi S, McCall AE, Jodice C, Persichetti F, Novelletto A, LeBorgne-DeMarquoy F, Duvick LA, Frontali M.
    Am J Hum Genet; 1993 Aug; 53(2):391-400. PubMed ID: 8101039
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  • 16. Genetic linkage mapping for a susceptibility locus to bipolar illness: chromosomes 2, 3, 4, 7, 9, 10p, 11p, 22, and Xpter.
    Detera-Wadleigh SD, Hsieh WT, Berrettini WH, Goldin LR, Rollins DY, Muniec D, Grewal R, Guroff JJ, Turner G, Coffman D.
    Am J Med Genet; 1994 Sep 15; 54(3):206-18. PubMed ID: 7810578
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  • 17. Spinocerebellar ataxia 1 (SCA1) in the Japanese in Hokkaido may derive from a single common ancestry.
    Wakisaka A, Sasaki H, Takada A, Fukazawa T, Suzuki Y, Hamada T, Iwabuchi K, Tashiro K, Yoshiki T.
    J Med Genet; 1995 Aug 15; 32(8):590-2. PubMed ID: 7473647
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  • 18. Autosomal dominant spinocerebellar ataxia: locus heterogeneity in a Nebraska kindred.
    Ranum LP, Rich SS, Nance MA, Duvick LA, Aita JF, Orr HT, Anton-Johnson S, Schut LJ.
    Neurology; 1992 Feb 15; 42(2):344-7. PubMed ID: 1736163
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  • 19. Machado-Joseph disease: an autosomal dominant motor system degeneration.
    Rosenberg RN.
    Mov Disord; 1992 Feb 15; 7(3):193-203. PubMed ID: 1620135
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  • 20. [Neuropathological study of autosomal dominant ataxia linked to loci on chromosome 6p (SCA 1)].
    Hamada K, Fukazawa T, Yanagihara T, Hamada T, Yoshida K, Sasaki H, Tashiro K.
    No To Shinkei; 1993 Nov 15; 45(11):1045-9. PubMed ID: 8297664
    [Abstract] [Full Text] [Related]

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