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Journal Abstract Search

168 related items for PubMed ID: 1585797

  • 1. HLA-linked spinocerebellar ataxia: a clinical and genetic study of large Italian kindreds.
    Spadaro M, Giunti P, Lulli P, Frontali M, Jodice C, Cappellacci S, Morellini M, Persichetti F, Trabace S, Anastasi R.
    Acta Neurol Scand; 1992 Apr; 85(4):257-65. PubMed ID: 1585797
    [Abstract] [Full Text] [Related]

  • 2. Clinical study of large kindreds with autosomal dominant HLA-linked spinocerebellar ataxia (SCA1) of late onset.
    Spadaro M, Giunti P, Colazza GB, Naso F, Bianco F, Morocutti C.
    Ital J Neurol Sci; 1993 Jan; 14(1):17-21. PubMed ID: 8473149
    [Abstract] [Full Text] [Related]

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

  • 4. Localization of the autosomal dominant HLA-linked spinocerebellar ataxia (SCA1) locus, in two kindreds, within an 8-cM subregion of chromosome 6p.
    Ranum LP, Duvick LA, Rich SS, Schut LJ, Litt M, Orr HT.
    Am J Hum Genet; 1991 Jul; 49(1):31-41. PubMed ID: 1676561
    [Abstract] [Full Text] [Related]

  • 5. 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]

  • 6. A gene on SCA4 locus causes dominantly inherited pure cerebellar ataxia.
    Nagaoka U, Takashima M, Ishikawa K, Yoshizawa K, Yoshizawa T, Ishikawa M, Yamawaki T, Shoji S, Mizusawa H.
    Neurology; 2000 May 23; 54(10):1971-5. PubMed ID: 10822439
    [Abstract] [Full Text] [Related]

  • 7. Multipoint linkage analysis of spinocerebellar ataxia and markers on chromosome 6.
    Haines JL, Trofatter JA.
    Genet Epidemiol; 1986 May 23; 3(6):399-405. PubMed ID: 3468044
    [Abstract] [Full Text] [Related]

  • 8. Linkage analysis between familial myoclonus epilepsy and short arm of chromosome 6 using HLA phenotype as genetic marker.
    Hashimoto O, Honda M, Niwa S, Kameyama T, Kumagai N, Nagakubo S, Shirayama Y, Hata A, Fukuda M, Anzai N.
    Jpn J Psychiatry Neurol; 1993 Jun 23; 47(2):275-7. PubMed ID: 8271562
    [No Abstract] [Full Text] [Related]

  • 9. 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 23; 42(2):344-7. PubMed ID: 1736163
    [Abstract] [Full Text] [Related]

  • 10. 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 23; 44(2):255-63. PubMed ID: 2563195
    [Abstract] [Full Text] [Related]

  • 11. Autosomal dominant ataxia: genetic evidence for locus heterogeneity from a Cuban founder-effect population.
    Auburger G, Diaz GO, Capote RF, Sanchez SG, Perez MP, del Cueto ME, Meneses MG, Farrall M, Williamson R, Chamberlain S.
    Am J Hum Genet; 1990 Jun 23; 46(6):1163-77. PubMed ID: 1971152
    [Abstract] [Full Text] [Related]

  • 12. Adult-onset autosomal recessive ataxia with thalamic lesions in a Finnish family.
    Rantamäki M, Krahe R, Paetau A, Cormand B, Mononen I, Udd B.
    Neurology; 2001 Sep 25; 57(6):1043-9. PubMed ID: 11571332
    [Abstract] [Full Text] [Related]

  • 13. Spinocerebellar ataxia (SCA1) in two large Italian kindreds: evidence in favour of a locus position distal to GLO1 and the HLA cluster.
    Frontali M, Iodice C, Lulli P, Spadaro M, Cappellacci S, Giunti P, Malaspina P, Morellini M, Morocutti C, Novelletto A.
    Ann Hum Genet; 1991 Jan 25; 55(1):7-15. PubMed ID: 1675045
    [Abstract] [Full Text] [Related]

  • 14. [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 Jan 25; 60(5):176-9. PubMed ID: 2100035
    [Abstract] [Full Text] [Related]

  • 15. 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 Jan 25; 60(1):37-9. PubMed ID: 1582256
    [Abstract] [Full Text] [Related]

  • 16. Presymptomatic testing for autosomal dominant spinocerebellar ataxia type 1.
    Shrimpton AE, Davidson R, MacDonald N, Brock DJ.
    J Med Genet; 1993 Jul 25; 30(7):616-7. PubMed ID: 8411042
    [Abstract] [Full Text] [Related]

  • 17. Adult onset spinocerebellar ataxia linked to HLA in a South African kindred of mixed ancestry.
    Bryer A, Martell RW, du Toit ED, Beighton P.
    Tissue Antigens; 1992 Sep 25; 40(3):111-5. PubMed ID: 1440565
    [Abstract] [Full Text] [Related]

  • 18. 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 25; 49(1):23-30. PubMed ID: 2063871
    [Abstract] [Full Text] [Related]

  • 19. Late onset autosomal dominant cerebellar ataxia. A family description and linkage analysis with the HLA system.
    Arruda WO, Petzl-Erler ML, Cardoso MA, Lehner T, Ott J.
    Arq Neuropsiquiatr; 1991 Sep 25; 49(3):285-91. PubMed ID: 1807228
    [Abstract] [Full Text] [Related]

  • 20. Machado-Joseph disease: an autosomal dominant motor system degeneration.
    Rosenberg RN.
    Mov Disord; 1992 Sep 25; 7(3):193-203. PubMed ID: 1620135
    [Abstract] [Full Text] [Related]

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