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Journal Abstract Search

172 related items for PubMed ID: 10072060

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

  • 2. 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]

  • 3. Mapping of a new autosomal dominant spinocerebellar ataxia to chromosome 22.
    Zu L, Figueroa KP, Grewal R, Pulst SM.
    Am J Hum Genet; 1999 Feb 23; 64(2):594-9. PubMed ID: 9973298
    [Abstract] [Full Text] [Related]

  • 4. A novel autosomal dominant spinocerebellar ataxia (SCA22) linked to chromosome 1p21-q23.
    Chung MY, Lu YC, Cheng NC, Soong BW.
    Brain; 2003 Jun 23; 126(Pt 6):1293-9. PubMed ID: 12764052
    [Abstract] [Full Text] [Related]

  • 5. Clinical and genetic analysis of a Tunisian family with autosomal dominant cerebellar ataxia type 1 linked to the SCA2 locus.
    Belal S, Cancel G, Stevanin G, Hentati F, Khati C, Ben Hamida C, Auburger G, Agid Y, Ben Hamida M, Brice A.
    Neurology; 1994 Aug 23; 44(8):1423-6. PubMed ID: 8058142
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  • 7. Multipoint linkage analysis of spinocerebellar ataxia and markers on chromosome 6.
    Haines JL, Trofatter JA.
    Genet Epidemiol; 1986 Aug 23; 3(6):399-405. PubMed ID: 3468044
    [Abstract] [Full Text] [Related]

  • 8. Genetic localization of the Ca2+ channel gene CACNG2 near SCA10 on chromosome 22q13.
    Burgess DL, Matsuura T, Ashizawa T, Noebels JL.
    Epilepsia; 2000 Jan 23; 41(1):24-7. PubMed ID: 10643919
    [Abstract] [Full Text] [Related]

  • 9. Clinical and genetic analysis of a distinct autosomal dominant spinocerebellar ataxia.
    Grewal RP, Tayag E, Figueroa KP, Zu L, Durazo A, Nunez C, Pulst SM.
    Neurology; 1998 Nov 23; 51(5):1423-6. PubMed ID: 9818872
    [Abstract] [Full Text] [Related]

  • 10. 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 23; 41(4):524-31. PubMed ID: 3477955
    [Abstract] [Full Text] [Related]

  • 11. A new dominant spinocerebellar ataxia linked to chromosome 19q13.4-qter.
    Brkanac Z, Bylenok L, Fernandez M, Matsushita M, Lipe H, Wolff J, Nochlin D, Raskind WH, Bird TD.
    Arch Neurol; 2002 Aug 23; 59(8):1291-5. PubMed ID: 12164726
    [Abstract] [Full Text] [Related]

  • 12. 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 23; 4(3):295-9. PubMed ID: 8358438
    [Abstract] [Full Text] [Related]

  • 13. Autosomal dominant cerebellar ataxia type I in Martinique (French West Indies): genetic analysis of three unrelated SCA2 families.
    Lezin A, Cancel G, Stevanin G, Smadja D, Vernant JC, Dürr A, Martial J, Buisson GG, Bellance R, Chneiweiss H, Agid Y, Brice A.
    Hum Genet; 1996 May 23; 97(5):671-6. PubMed ID: 8655151
    [Abstract] [Full Text] [Related]

  • 14. An expanded CAG repeat sequence in spinocerebellar ataxia type 7.
    Lindblad K, Savontaus ML, Stevanin G, Holmberg M, Digre K, Zander C, Ehrsson H, David G, Benomar A, Nikoskelainen E, Trottier Y, Holmgren G, Ptacek LJ, Anttinen A, Brice A, Schalling M.
    Genome Res; 1996 Oct 23; 6(10):965-71. PubMed ID: 8908515
    [Abstract] [Full Text] [Related]

  • 15. Spinocerebellar ataxia type 6: genotype and phenotype in German kindreds.
    Schöls L, Krüger R, Amoiridis G, Przuntek H, Epplen JT, Riess O.
    J Neurol Neurosurg Psychiatry; 1998 Jan 23; 64(1):67-73. PubMed ID: 9436730
    [Abstract] [Full Text] [Related]

  • 16. Confirmation of the SCA-2 locus as an alternative locus for dominantly inherited spinocerebellar ataxias and refinement of the candidate region.
    Lopes-Cendes I, Andermann E, Attig E, Cendes F, Bosch S, Wagner M, Gerstenbrand F, Andermann F, Rouleau GA.
    Am J Hum Genet; 1994 May 23; 54(5):774-81. PubMed ID: 8178818
    [Abstract] [Full Text] [Related]

  • 17. A novel locus for dominant cerebellar ataxia (SCA14) maps to a 10.2-cM interval flanked by D19S206 and D19S605 on chromosome 19q13.4-qter.
    Yamashita I, Sasaki H, Yabe I, Fukazawa T, Nogoshi S, Komeichi K, Takada A, Shiraishi K, Takiyama Y, Nishizawa M, Kaneko J, Tanaka H, Tsuji S, Tashiro K.
    Ann Neurol; 2000 Aug 23; 48(2):156-63. PubMed ID: 10939565
    [Abstract] [Full Text] [Related]

  • 18. 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 23; 3(1):177-80. PubMed ID: 8162021
    [Abstract] [Full Text] [Related]

  • 19. Autosomal dominant cerebellar ataxia type III: linkage in a large British family to a 7.6-cM region on chromosome 15q14-21.3.
    Worth PF, Giunti P, Gardner-Thorpe C, Dixon PH, Davis MB, Wood NW.
    Am J Hum Genet; 1999 Aug 23; 65(2):420-6. PubMed ID: 10417284
    [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 23; 91(4):362-6. PubMed ID: 8099059
    [Abstract] [Full Text] [Related]

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