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Journal Abstract Search

279 related items for PubMed ID: 12384780

  • 1. Identification of a novel SCA locus ( SCA19) in a Dutch autosomal dominant cerebellar ataxia family on chromosome region 1p21-q21.
    Verbeek DS, Schelhaas JH, Ippel EF, Beemer FA, Pearson PL, Sinke RJ.
    Hum Genet; 2002 Oct; 111(4-5):388-93. PubMed ID: 12384780
    [Abstract] [Full Text] [Related]

  • 2. Mapping of the SCA23 locus involved in autosomal dominant cerebellar ataxia to chromosome region 20p13-12.3.
    Verbeek DS, van de Warrenburg BP, Wesseling P, Pearson PL, Kremer HP, Sinke RJ.
    Brain; 2004 Nov; 127(Pt 11):2551-7. PubMed ID: 15306549
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  • 3. An autosomal dominant ataxia maps to 19q13: Allelic heterogeneity of SCA13 or novel locus?
    Waters MF, Fee D, Figueroa KP, Nolte D, Müller U, Advincula J, Coon H, Evidente VG, Pulst SM.
    Neurology; 2005 Oct 11; 65(7):1111-3. PubMed ID: 16135769
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  • 4. Spinocerebellar ataxia with sensory neuropathy (SCA25) maps to chromosome 2p.
    Stevanin G, Bouslam N, Thobois S, Azzedine H, Ravaux L, Boland A, Schalling M, Broussolle E, Dürr A, Brice A.
    Ann Neurol; 2004 Jan 11; 55(1):97-104. PubMed ID: 14705117
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  • 5. The gene for autosomal dominant cerebellar ataxia with pigmentary macular dystrophy maps to chromosome 3p12-p21.1.
    Benomar A, Krols L, Stevanin G, Cancel G, LeGuern E, David G, Ouhabi H, Martin JJ, Dürr A, Zaim A.
    Nat Genet; 1995 May 11; 10(1):84-8. PubMed ID: 7647798
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  • 6. Physical map and haplotype analysis of 16q-linked autosomal dominant cerebellar ataxia (ADCA) type III in Japan.
    Li M, Ishikawa K, Toru S, Tomimitsu H, Takashima M, Goto J, Takiyama Y, Sasaki H, Imoto I, Inazawa J, Toda T, Kanazawa I, Mizusawa H.
    J Hum Genet; 2003 May 11; 48(3):111-8. PubMed ID: 12624721
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  • 7. Autosomal-dominant cerebellar ataxia with retinal degeneration (ADCA type II) is genetically different from ADCA type I.
    Benomar A, Le Guern E, Dürr A, Ouhabi H, Stevanin G, Yahyaoui M, Chkili T, Agid Y, Brice A.
    Ann Neurol; 1994 Apr 11; 35(4):439-44. PubMed ID: 8154871
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  • 8. [Autosomal dominant cerebellar ataxias in the Netherlands: a national inventory].
    van de Warrenburg BP.
    Ned Tijdschr Geneeskd; 2001 May 19; 145(20):962-7. PubMed ID: 11396263
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  • 9. A linkage disequilibrium at the candidate gene locus for 16q-linked autosomal dominant cerebellar ataxia type III in Japan.
    Takashima M, Ishikawa K, Nagaoka U, Shoji S, Mizusawa H.
    J Hum Genet; 2001 May 19; 46(4):167-71. PubMed ID: 11322654
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  • 11. A novel autosomal dominant spinocerebellar ataxia (SCA22) linked to chromosome 1p21-q23.
    Chung MY, Lu YC, Cheng NC, Soong BW.
    Brain; 2003 Jun 19; 126(Pt 6):1293-9. PubMed ID: 12764052
    [Abstract] [Full Text] [Related]

  • 12. Spinocerebellar ataxia type 26 maps to chromosome 19p13.3 adjacent to SCA6.
    Yu GY, Howell MJ, Roller MJ, Xie TD, Gomez CM.
    Ann Neurol; 2005 Mar 19; 57(3):349-54. PubMed ID: 15732118
    [Abstract] [Full Text] [Related]

  • 13. Autosomal dominant sensory/motor neuropathy with Ataxia (SMNA): Linkage to chromosome 7q22-q32.
    Brkanac Z, Fernandez M, Matsushita M, Lipe H, Wolff J, Bird TD, Raskind WH.
    Am J Med Genet; 2002 May 08; 114(4):450-7. PubMed ID: 11992570
    [Abstract] [Full Text] [Related]

  • 14. Autosomal dominant cerebellar ataxias in Spain: molecular and clinical correlations, prevalence estimation and survival analysis.
    Infante J, Combarros O, Volpini V, Corral J, Llorca J, Berciano J.
    Acta Neurol Scand; 2005 Jun 08; 111(6):391-9. PubMed ID: 15876341
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  • 15. 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 08; 65(2):420-6. PubMed ID: 10417284
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  • 16. Clinical and genetic epidemiological study of 16q22.1-linked autosomal dominant cerebellar ataxia in western Japan.
    Hayashi M, Adachi Y, Mori M, Nakano T, Nakashima K.
    Acta Neurol Scand; 2007 Aug 08; 116(2):123-7. PubMed ID: 17661799
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  • 19. A novel locus for autosomal dominant nonsyndromic hearing loss (DFNA44) maps to chromosome 3q28-29.
    Modamio-Høybjør S, Moreno-Pelayo MA, Mencía A, del Castillo I, Chardenoux S, Armenta D, Lathrop M, Petit C, Moreno F.
    Hum Genet; 2003 Jan 08; 112(1):24-8. PubMed ID: 12483295
    [Abstract] [Full Text] [Related]

  • 20. Evidence for linkage of restless legs syndrome to chromosome 9p: are there two distinct loci?
    Lohmann-Hedrich K, Neumann A, Kleensang A, Lohnau T, Muhle H, Djarmati A, König IR, Pramstaller PP, Schwinger E, Kramer PL, Ziegler A, Stephani U, Klein C.
    Neurology; 2008 Feb 26; 70(9):686-94. PubMed ID: 18032746
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