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147 related items for PubMed ID: 1628431

  • 1. [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
    [Abstract] [Full Text] [Related]

  • 2. [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
    [Abstract] [Full Text] [Related]

  • 3. The gene for Machado-Joseph disease maps to human chromosome 14q.
    Takiyama Y, Nishizawa M, Tanaka H, Kawashima S, Sakamoto H, Karube Y, Shimazaki H, Soutome M, Endo K, Ohta S.
    Nat Genet; 1993 Jul; 4(3):300-4. PubMed ID: 8358439
    [Abstract] [Full Text] [Related]

  • 4. The Machado-Joseph disease locus is different from the spinocerebellar ataxia locus (SCA1).
    Carson WJ, Radvany J, Farrer LA, Vincent D, Rosenberg RN, MacLeod PM, Rouleau GA.
    Genomics; 1992 Jul; 13(3):852-5. PubMed ID: 1639414
    [Abstract] [Full Text] [Related]

  • 5. 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
    [Abstract] [Full Text] [Related]

  • 6. [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]

  • 7. [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]

  • 8. Evidence for the existence of a fourth dominantly inherited spinocerebellar ataxia locus.
    Lopes-Cendes I, Andermann E, Rouleau GA.
    Genomics; 1994 May 01; 21(1):270-4. PubMed ID: 8088802
    [Abstract] [Full Text] [Related]

  • 9. Linkage studies in spinocerebellar ataxia (SCA).
    Morton NE, Lalouel JM, Jackson JF, Currier RD, Yee S.
    Am J Med Genet; 1980 May 01; 6(3):251-7. PubMed ID: 7424977
    [Abstract] [Full Text] [Related]

  • 10. [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 01; 42(11):1103-11. PubMed ID: 2076357
    [Abstract] [Full Text] [Related]

  • 11. [Linkage study of hereditary spinocerebellar ataxia, and probable correlation for the loci to the disease phenotypes].
    Sasaki H.
    Rinsho Shinkeigaku; 1993 Dec 01; 33(12):1285-7. PubMed ID: 8174326
    [Abstract] [Full Text] [Related]

  • 12. [Recent progress of research on hereditary spinocerebellar degeneration].
    Wakisaka A, Sasaki H.
    Nihon Rinsho; 1993 Sep 01; 51(9):2467-73. PubMed ID: 8411730
    [Abstract] [Full Text] [Related]

  • 13. Expanded CAG repeats in spinocerebellar ataxia (SCA1) segregate with distinct haplotypes in South african families.
    Ramesar RS, Bardien S, Beighton P, Bryer A.
    Hum Genet; 1997 Jul 01; 100(1):131-7. PubMed ID: 9225982
    [Abstract] [Full Text] [Related]

  • 14. 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 01; 53(2):391-400. PubMed ID: 8101039
    [Abstract] [Full Text] [Related]

  • 15. 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 01; 126(2):310-2. PubMed ID: 7925830
    [Abstract] [Full Text] [Related]

  • 16. Molecular genetics of hereditary ataxias.
    Banfi S, Zoghbi HY.
    Baillieres Clin Neurol; 1994 Aug 01; 3(2):281-95. PubMed ID: 7952848
    [Abstract] [Full Text] [Related]

  • 17. 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 01; 49(1):23-30. PubMed ID: 2063871
    [Abstract] [Full Text] [Related]

  • 18. Molecular and clinical correlations in spinocerebellar ataxia type 3 and Machado-Joseph disease.
    Matilla T, McCall A, Subramony SH, Zoghbi HY.
    Ann Neurol; 1995 Jul 01; 38(1):68-72. PubMed ID: 7611728
    [Abstract] [Full Text] [Related]

  • 19. Machado Joseph disease is not an allele of the spinocerebellar ataxia 2 locus.
    Twist EC, Farrer LA, Macleod PM, Radvany J, Chamberlain S, Rosenberg RN, Rouleau GA.
    Hum Genet; 1994 Mar 01; 93(3):335-8. PubMed ID: 8125487
    [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 01; 11(2):174-80. PubMed ID: 8684388
    [Abstract] [Full Text] [Related]

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