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Journal Abstract Search

147 related items for PubMed ID: 7925830

  • 21. [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; 127(5-6):157-62. PubMed ID: 10500422
    [Abstract] [Full Text] [Related]

  • 22. [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; 45(11):1045-9. PubMed ID: 8297664
    [Abstract] [Full Text] [Related]

  • 23. [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]

  • 24. Analysis of spinocerebellar ataxia type 2 gene and haplotype analysis: (CCG)1-2 polymorphism and contribution to founder effect.
    Mizushima K, Watanabe M, Kondo I, Okamoto K, Shizuka M, Abe K, Aoki M, Shoji M.
    J Med Genet; 1999 Feb; 36(2):112-4. PubMed ID: 10051008
    [Abstract] [Full Text] [Related]

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

  • 26. 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
    [Abstract] [Full Text] [Related]

  • 27. A 17th-century founder gives rise to a large north American pedigree of autosomal dominant spinocerebellar ataxia not linked to the SCA1 locus on chromosome 6.
    Lazzarini A, Zimmerman TR, Johnson WG, Duvoisin RC.
    Neurology; 1992 Nov; 42(11):2118-24. PubMed ID: 1436521
    [Abstract] [Full Text] [Related]

  • 28. [Spinocerebellar ataxia: advances in genetic research and its clinical implication].
    Sasaki H.
    Hokkaido Igaku Zasshi; 1997 Jan; 72(1):13-20. PubMed ID: 9086358
    [Abstract] [Full Text] [Related]

  • 29. 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; 93(3):335-8. PubMed ID: 8125487
    [Abstract] [Full Text] [Related]

  • 30. Presymptomatic analysis of spinocerebellar ataxia type 1 (SCA1) via the expansion of the SCA1 CAG-repeat in a large pedigree displaying anticipation and parental male bias.
    Matilla T, Volpini V, Genís D, Rosell J, Corral J, Dávalos A, Molins A, Estivill X.
    Hum Mol Genet; 1993 Dec; 2(12):2123-8. PubMed ID: 8111382
    [Abstract] [Full Text] [Related]

  • 31. 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; 42(2):344-7. PubMed ID: 1736163
    [Abstract] [Full Text] [Related]

  • 32. Spinocerebellar ataxia: localization of an autosomal dominant locus between two markers on human chromosome 6.
    Rich SS, Wilkie P, Schut L, Vance G, Orr HT.
    Am J Hum Genet; 1987 Oct; 41(4):524-31. PubMed ID: 3477955
    [Abstract] [Full Text] [Related]

  • 33. [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]

  • 34. Mapping and cloning of the critical region for the spinocerebellar ataxia type 1 gene (SCA1) in a yeast artificial chromosome contig spanning 1.2 Mb.
    Banfi S, Chung MY, Kwiatkowski TJ, Ranum LP, McCall AE, Chinault AC, Orr HT, Zoghbi HY.
    Genomics; 1993 Dec; 18(3):627-35. PubMed ID: 8307572
    [Abstract] [Full Text] [Related]

  • 35. Tight linkage of the gene for spinocerebellar ataxia to D6S89 on the short arm of chromosome 6 in a kindred for which close linkage to both HLA and F13A1 is excluded.
    Keats BJ, Pollack MS, McCall A, Wilensky MA, Ward LJ, Lu M, Zoghbi HY.
    Am J Hum Genet; 1991 Nov; 49(5):972-7. PubMed ID: 1928103
    [Abstract] [Full Text] [Related]

  • 36. Assignment of autosomal dominant spinocerebellar ataxia (SCA1) centromeric to the HLA region on the short arm of chromosome 6, using multilocus linkage analysis.
    Zoghbi HY, Sandkuyl LA, Ott J, Daiger SP, Pollack M, O'Brien WE, Beaudet AL.
    Am J Hum Genet; 1989 Feb; 44(2):255-63. PubMed ID: 2563195
    [Abstract] [Full Text] [Related]

  • 37. 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]

  • 38. A gene for autosomal dominant paroxysmal choreoathetosis/spasticity (CSE) maps to the vicinity of a potassium channel gene cluster on chromosome 1p, probably within 2 cM between D1S443 and D1S197.
    Auburger G, Ratzlaff T, Lunkes A, Nelles HW, Leube B, Binkofski F, Kugel H, Heindel W, Seitz R, Benecke R, Witte OW, Voit T.
    Genomics; 1996 Jan 01; 31(1):90-4. PubMed ID: 8808284
    [Abstract] [Full Text] [Related]

  • 39. Spinocerebellar ataxia: multipoint linkage analysis of genes associated with the disease locus.
    Wilkie PJ, Schut LJ, Rich SS.
    Hum Genet; 1991 Aug 01; 87(4):405-8. PubMed ID: 1879827
    [Abstract] [Full Text] [Related]

  • 40. Autosomal dominant cerebellar ataxia with dementia: evidence for a fourth disease locus.
    Twells R, Yenchitsomanus PT, Sirinavin C, Allotey R, Poungvarin N, Viriyavejakul A, Cemal C, Weber J, Farrall M, Rodprasert P.
    Hum Mol Genet; 1994 Jan 01; 3(1):177-80. PubMed ID: 8162021
    [Abstract] [Full Text] [Related]

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