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Journal Abstract Search

75 related items for PubMed ID: 8242075

  • 1. Endothelin 1 is not a candidate gene for spinal cerebellar ataxia 1.
    Cancel G, Khati C, Stevanin G, Pages JC, Agid Y, Brice A, Cann HM.
    Hum Mol Genet; 1993 Sep; 2(9):1477-9. PubMed ID: 8242075
    [No Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. 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; 3(1):177-80. PubMed ID: 8162021
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  • 5. Mapping of the gene for a novel spinocerebellar ataxia with pure cerebellar signs and epilepsy.
    Matsuura T, Achari M, Khajavi M, Bachinski LL, Zoghbi HY, Ashizawa T.
    Ann Neurol; 1999 Mar; 45(3):407-11. PubMed ID: 10072060
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  • 7. 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; 32(8):590-2. PubMed ID: 7473647
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  • 8. Multipoint linkage analysis of spinocerebellar ataxia and markers on chromosome 6.
    Haines JL, Trofatter JA.
    Genet Epidemiol; 1986 Aug; 3(6):399-405. PubMed ID: 3468044
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  • 9. Presymptomatic testing for autosomal dominant spinocerebellar ataxia type 1.
    Shrimpton AE, Davidson R, MacDonald N, Brock DJ.
    J Med Genet; 1993 Jul; 30(7):616-7. PubMed ID: 8411042
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  • 12. Spinocerebellar ataxia type 5 in a family descended from the grandparents of President Lincoln maps to chromosome 11.
    Ranum LP, Schut LJ, Lundgren JK, Orr HT, Livingston DM.
    Nat Genet; 1994 Nov; 8(3):280-4. PubMed ID: 7874171
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  • 13. 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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  • 14. Ataxias on the march from Quebec to Tunisia.
    Pulst SM, Filla A.
    Neurology; 2000 Apr 11; 54(7):1400-1. PubMed ID: 10751244
    [No Abstract] [Full Text] [Related]

  • 15. Anticipation in spinocerebellar ataxia type 2.
    Pulst SM, Nechiporuk A, Starkman S.
    Nat Genet; 1993 Sep 11; 5(1):8-10. PubMed ID: 8220431
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  • 16. Infantile onset spinocerebellar ataxia represents an allelic disease distinct from other hereditary ataxias.
    Nikali K, Koskinen T, Suomalainen A, Pihko H, Peltonen L.
    Pediatr Res; 1994 Nov 11; 36(5):607-12. PubMed ID: 7877879
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  • 17. 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 11; 4(3):221-6. PubMed ID: 8358429
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  • 18. Posterior column ataxia and retinitis pigmentosa: a distinct clinical and genetic disorder.
    Higgins JJ, Kluetzman K, Berciano J, Combarros O, Loveless JM.
    Mov Disord; 2000 May 11; 15(3):575-8. PubMed ID: 10830426
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  • 19. [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 11; 32(1):13-6. PubMed ID: 1628431
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  • 20. 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 11; 2(12):2123-8. PubMed ID: 8111382
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