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Journal Abstract Search

242 related items for PubMed ID: 10822439

  • 1. 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]

  • 2. 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 23; 46(4):167-71. PubMed ID: 11322654
    [Abstract] [Full Text] [Related]

  • 3. Fine mapping of 16q-linked autosomal dominant cerebellar ataxia type III in Japanese families.
    Hirano R, Takashima H, Okubo R, Tajima K, Okamoto Y, Ishida S, Tsuruta K, Arisato T, Arata H, Nakagawa M, Osame M, Arimura K.
    Neurogenetics; 2004 Dec 23; 5(4):215-21. PubMed ID: 15455264
    [Abstract] [Full Text] [Related]

  • 4. 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 Dec 23; 48(3):111-8. PubMed ID: 12624721
    [Abstract] [Full Text] [Related]

  • 5. Clinical features of chromosome 16q22.1 linked autosomal dominant cerebellar ataxia in Japanese.
    Onodera Y, Aoki M, Mizuno H, Warita H, Shiga Y, Itoyama Y.
    Neurology; 2006 Oct 10; 67(7):1300-2. PubMed ID: 17030774
    [Abstract] [Full Text] [Related]

  • 6. 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 10; 65(2):420-6. PubMed ID: 10417284
    [Abstract] [Full Text] [Related]

  • 7. 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 10; 111(4-5):388-93. PubMed ID: 12384780
    [Abstract] [Full Text] [Related]

  • 8. [Autosomal dominant cortical cerebellar atrophy (ADCCA) linked to chromosome 16q].
    Ishikawa K.
    Rinsho Shinkeigaku; 2001 Dec 10; 41(12):1117-9. PubMed ID: 12235813
    [Abstract] [Full Text] [Related]

  • 9. Localization of autosomal dominant cerebellar ataxia associated with retinal degeneration and anticipation to chromosome 3p12-p21.1.
    Holmberg M, Johansson J, Forsgren L, Heijbel J, Sandgren O, Holmgren G.
    Hum Mol Genet; 1995 Aug 10; 4(8):1441-5. PubMed ID: 7581386
    [Abstract] [Full Text] [Related]

  • 10. 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 10; 4(3):295-9. PubMed ID: 8358438
    [Abstract] [Full Text] [Related]

  • 11. Autosomal dominant congenital non-progressive ataxia overlaps with the SCA15 locus.
    Dudding TE, Friend K, Schofield PW, Lee S, Wilkinson IA, Richards RI.
    Neurology; 2004 Dec 28; 63(12):2288-92. PubMed ID: 15623688
    [Abstract] [Full Text] [Related]

  • 12. 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 28; 45(3):407-11. PubMed ID: 10072060
    [Abstract] [Full Text] [Related]

  • 13. A novel autosomal dominant spinocerebellar ataxia (SCA22) linked to chromosome 1p21-q23.
    Chung MY, Lu YC, Cheng NC, Soong BW.
    Brain; 2003 Jun 28; 126(Pt 6):1293-9. PubMed ID: 12764052
    [Abstract] [Full Text] [Related]

  • 14. Search for the chromosomal location of autosomal dominant cerebellar ataxia from Holguin, Cuba: exclusion from candidate regions on chromosome 4 and 11q.
    Gispert S, Nothers C, Orozco G, Auburger G.
    Hum Hered; 1993 Jun 28; 43(1):12-20. PubMed ID: 8514320
    [Abstract] [Full Text] [Related]

  • 15. 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 28; 51(5):1423-6. PubMed ID: 9818872
    [Abstract] [Full Text] [Related]

  • 16. A third locus for autosomal dominant cerebellar ataxia type I maps to chromosome 14q24.3-qter: evidence for the existence of a fourth locus.
    Stevanin G, Le Guern E, Ravisé N, Chneiweiss H, Dürr A, Cancel G, Vignal A, Boch AL, Ruberg M, Penet C.
    Am J Hum Genet; 1994 Jan 28; 54(1):11-20. PubMed ID: 8279460
    [Abstract] [Full Text] [Related]

  • 17. 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 28; 85(4):257-65. PubMed ID: 1585797
    [Abstract] [Full Text] [Related]

  • 18. 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 28; 35(4):439-44. PubMed ID: 8154871
    [Abstract] [Full Text] [Related]

  • 19. 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 28; 44(8):1423-6. PubMed ID: 8058142
    [Abstract] [Full Text] [Related]

  • 20. 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 28; 116(2):123-7. PubMed ID: 17661799
    [Abstract] [Full Text] [Related]

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