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Journal Abstract Search

147 related items for PubMed ID: 7925830

  • 1. 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]

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

  • 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
    [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. Evidence for a mechanism predisposing to intergenerational CAG repeat instability in spinocerebellar ataxia type I.
    Chung MY, Ranum LP, Duvick LA, Servadio A, Zoghbi HY, Orr HT.
    Nat Genet; 1993 Nov; 5(3):254-8. PubMed ID: 8275090
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  • 7. [Clinical study of two families with late-onset autosomal dominant spinal-cerebellar ataxia linked with HLA. Preliminary results].
    Giunti P, Spadaro M, Frontali M, Bianco F, Morocutti C.
    Riv Neurol; 1990 Nov; 60(5):176-9. PubMed ID: 2100035
    [Abstract] [Full Text] [Related]

  • 8. The gene for spinal cerebellar ataxia 1 (SCA1) is flanked by two closely linked highly polymorphic microsatellite loci.
    Jodice C, Frontali M, Persichetti F, Novelletto A, Pandolfo M, Spadaro M, Giunti P, Schinaia G, Lulli P, Malaspina P.
    Hum Mol Genet; 1993 Sep; 2(9):1383-7. PubMed ID: 8242061
    [Abstract] [Full Text] [Related]

  • 9. Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1.
    Orr HT, Chung MY, Banfi S, Kwiatkowski TJ, Servadio A, Beaudet AL, McCall AE, Duvick LA, Ranum LP, Zoghbi HY.
    Nat Genet; 1993 Jul; 4(3):221-6. PubMed ID: 8358429
    [Abstract] [Full Text] [Related]

  • 10. Regional mapping of the gene for autosomal dominant spinocerebellar ataxia (SCA1) by localizing the closely linked D6S89 locus to 6p24.2----p23.05.
    Volz A, Fonatsch C, Ziegler A.
    Cytogenet Cell Genet; 1992 Jul; 60(1):37-9. PubMed ID: 1582256
    [Abstract] [Full Text] [Related]

  • 11. 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]

  • 12. 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
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  • 14. Unstable triplet repeat and phenotypic variability of spinocerebellar ataxia type 1.
    Goldfarb LG, Vasconcelos O, Platonov FA, Lunkes A, Kipnis V, Kononova S, Chabrashvili T, Vladimirtsev VA, Alexeev VP, Gajdusek DC.
    Ann Neurol; 1996 Apr 01; 39(4):500-6. PubMed ID: 8619528
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  • 16. 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]

  • 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 01; 32(8):590-2. PubMed ID: 7473647
    [Abstract] [Full Text] [Related]

  • 18. Recent results in ataxia research.
    Giunti P, Spadaro M, Colazza GB, Morocutti C.
    Riv Neurol; 1991 Aug 01; 61(4):154-7. PubMed ID: 1815314
    [Abstract] [Full Text] [Related]

  • 19. [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 01; 32(1):17-22. PubMed ID: 1628432
    [Abstract] [Full Text] [Related]

  • 20. Molecular heterogeneity of autosomal dominant cerebellar ataxia: analysis of flanking microsatellites of the spinocerebellar ataxia 1 locus in a northern European family unequivocally demonstrates non-linkage.
    Lunkes A, Gispert S, Enczmann J, Auburger G.
    Hum Genet; 1993 May 01; 91(4):362-6. PubMed ID: 8099059
    [Abstract] [Full Text] [Related]

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