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Journal Abstract Search

755 related items for PubMed ID: 15895552

  • 1. The wide spectrum of spinocerebellar ataxias (SCAs).
    Manto MU.
    Cerebellum; 2005; 4(1):2-6. PubMed ID: 15895552
    [Abstract] [Full Text] [Related]

  • 2. Molecular genetics of hereditary spinocerebellar ataxia: mutation analysis of spinocerebellar ataxia genes and CAG/CTG repeat expansion detection in 225 Italian families.
    Brusco A, Gellera C, Cagnoli C, Saluto A, Castucci A, Michielotto C, Fetoni V, Mariotti C, Migone N, Di Donato S, Taroni F.
    Arch Neurol; 2004 May; 61(5):727-33. PubMed ID: 15148151
    [Abstract] [Full Text] [Related]

  • 3. Frequency of SCA1, SCA2, SCA3/MJD, SCA6, SCA7, and DRPLA CAG trinucleotide repeat expansion in patients with hereditary spinocerebellar ataxia from Chinese kindreds.
    Tang B, Liu C, Shen L, Dai H, Pan Q, Jing L, Ouyang S, Xia J.
    Arch Neurol; 2000 Apr; 57(4):540-4. PubMed ID: 10768629
    [Abstract] [Full Text] [Related]

  • 4. Analysis of SCA8, SCA10, SCA12, SCA17 and SCA19 in patients with unknown spinocerebellar ataxia: a Thai multicentre study.
    Choubtum L, Witoonpanich P, Hanchaiphiboolkul S, Bhidayasiri R, Jitkritsadakul O, Pongpakdee S, Wetchaphanphesat S, Boonkongchuen P, Pulkes T.
    BMC Neurol; 2015 Sep 15; 15():166. PubMed ID: 26374734
    [Abstract] [Full Text] [Related]

  • 5. Spinocerebellar ataxias in Spanish patients: genetic analysis of familial and sporadic cases. The Ataxia Study Group.
    Pujana MA, Corral J, Gratacòs M, Combarros O, Berciano J, Genís D, Banchs I, Estivill X, Volpini V.
    Hum Genet; 1999 Jun 15; 104(6):516-22. PubMed ID: 10453742
    [Abstract] [Full Text] [Related]

  • 6. Autosomal dominant cerebellar ataxia type I: a review of the phenotypic and genotypic characteristics.
    Whaley NR, Fujioka S, Wszolek ZK.
    Orphanet J Rare Dis; 2011 May 28; 6():33. PubMed ID: 21619691
    [Abstract] [Full Text] [Related]

  • 7. Analysis of CAG repeats in SCA1, SCA2, SCA3, SCA6, SCA7 and DRPLA loci in spinocerebellar ataxia patients and distribution of CAG repeats at the SCA1, SCA2 and SCA6 loci in nine ethnic populations of eastern India.
    Basu P, Chattopadhyay B, Gangopadhaya PK, Mukherjee SC, Sinha KK, Das SK, Roychoudhury S, Majumder PP, Bhattacharyya NP.
    Hum Genet; 2000 Jun 28; 106(6):597-604. PubMed ID: 10942107
    [Abstract] [Full Text] [Related]

  • 8. Analysis of spinocerebellar ataxias due to expanded triplet repeats in Greek patients with cerebellar ataxia.
    Koutsis G, Pemble S, Sweeney MG, Paudel R, Wood NW, Panas M, Kladi A, Houlden H.
    J Neurol Sci; 2012 Jul 15; 318(1-2):178-80. PubMed ID: 22520093
    [Abstract] [Full Text] [Related]

  • 9. The hereditary spinocerebellar ataxias in Japan.
    Sasaki H, Yabe I, Tashiro K.
    Cytogenet Genome Res; 2003 Jul 15; 100(1-4):198-205. PubMed ID: 14526181
    [Abstract] [Full Text] [Related]

  • 10. Analysis of SCA1, DRPLA, MJD, SCA2, and SCA6 CAG repeats in 48 Portuguese ataxia families.
    Silveira I, Coutinho P, Maciel P, Gaspar C, Hayes S, Dias A, Guimarães J, Loureiro L, Sequeiros J, Rouleau GA.
    Am J Med Genet; 1998 Mar 28; 81(2):134-8. PubMed ID: 9613852
    [Abstract] [Full Text] [Related]

  • 11. The occurrence of spinocerebellar ataxias caused by dynamic mutations in Polish patients.
    Sułek-Piatkowska A, Zdzienicka E, Raczyńska-Rakowicz M, Krysa W, Rajkiewicz M, Szirkowiec W, Zaremba J.
    Neurol Neurochir Pol; 2010 Mar 28; 44(3):238-45. PubMed ID: 20625959
    [Abstract] [Full Text] [Related]

  • 12. Molecular analysis of Spinocerebellar ataxias in Koreans: frequencies and reference ranges of SCA1, SCA2, SCA3, SCA6, and SCA7.
    Kim JY, Park SS, Joo SI, Kim JM, Jeon BS.
    Mol Cells; 2001 Dec 31; 12(3):336-41. PubMed ID: 11804332
    [Abstract] [Full Text] [Related]

  • 13. Spinocerebellar ataxias in Venezuela: genetic epidemiology and their most likely ethnic descent.
    Paradisi I, Ikonomu V, Arias S.
    J Hum Genet; 2016 Mar 31; 61(3):215-22. PubMed ID: 26538302
    [Abstract] [Full Text] [Related]

  • 14. Spinocerebellar ataxias in Brazil--frequencies and modulating effects of related genes.
    de Castilhos RM, Furtado GV, Gheno TC, Schaeffer P, Russo A, Barsottini O, Pedroso JL, Salarini DZ, Vargas FR, de Lima MA, Godeiro C, Santana-da-Silva LC, Toralles MB, Santos S, van der Linden H, Wanderley HY, de Medeiros PF, Pereira ET, Ribeiro E, Saraiva-Pereira ML, Jardim LB, Rede Neurogenetica.
    Cerebellum; 2014 Feb 31; 13(1):17-28. PubMed ID: 23943520
    [Abstract] [Full Text] [Related]

  • 15. Clinical and genetic analysis of spinocerebellar ataxia type 7 (SCA7) in Zambian families.
    Atadzhanov M, Smith DC, Mwaba MH, Siddiqi OK, Bryer A, Greenberg LJ.
    Cerebellum Ataxias; 2017 Feb 31; 4():17. PubMed ID: 29214039
    [Abstract] [Full Text] [Related]

  • 16. [CAG trinucleotide mutation detection in patients with hereditary spinocerebellar ataxia].
    Tang B, Xia J, Wang D, Tang X, Shen L, Liu C, Dai H, Yan X, Pan Q, Xiao J, Zhang B, Ou Y.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1999 Oct 31; 16(5):281-4. PubMed ID: 10514531
    [Abstract] [Full Text] [Related]

  • 17. [Autosomal dominant spinocerebellar ataxia].
    Legros B, Manto MU.
    Rev Med Brux; 1999 Dec 31; 20(6):495-503. PubMed ID: 10672773
    [Abstract] [Full Text] [Related]

  • 18. Spinocerebellar ataxia in a cohort of patients from Rio de Janeiro.
    Alvarenga MP, Siciliani LC, Carvalho RS, Ganimi MC, Penna PS.
    Neurol Sci; 2022 Aug 31; 43(8):4997-5005. PubMed ID: 35469073
    [Abstract] [Full Text] [Related]

  • 19. Frequency analysis and clinical characterization of spinocerebellar ataxia types 1, 2, 3, 6, and 7 in Korean patients.
    Lee WY, Jin DK, Oh MR, Lee JE, Song SM, Lee EA, Kim GM, Chung JS, Lee KH.
    Arch Neurol; 2003 Jun 31; 60(6):858-63. PubMed ID: 12810491
    [Abstract] [Full Text] [Related]

  • 20. A novel autosomal dominant spinocerebellar ataxia (SCA22) linked to chromosome 1p21-q23.
    Chung MY, Lu YC, Cheng NC, Soong BW.
    Brain; 2003 Jun 31; 126(Pt 6):1293-9. PubMed ID: 12764052
    [Abstract] [Full Text] [Related]

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