BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

116 related articles for article (PubMed ID: 14967764)

  • 1. Spinocerebellar ataxia type 17: latest member of polyglutamine disease group highlights unanswered questions.
    Tsuji S
    Arch Neurol; 2004 Feb; 61(2):183-4. PubMed ID: 14967764
    [No Abstract]   [Full Text] [Related]  

  • 2. Case of spinocerebellar ataxia type 17 (SCA17) associated with only 41 repeats of the TATA-binding protein (TBP) gene.
    Nanda A; Jackson SA; Schwankhaus JD; Metzer WS
    Mov Disord; 2007 Feb; 22(3):436. PubMed ID: 17149738
    [No Abstract]   [Full Text] [Related]  

  • 3. Possible reduced penetrance of expansion of 44 to 47 CAG/CAA repeats in the TATA-binding protein gene in spinocerebellar ataxia type 17.
    Oda M; Maruyama H; Komure O; Morino H; Terasawa H; Izumi Y; Imamura T; Yasuda M; Ichikawa K; Ogawa M; Matsumoto M; Kawakami H
    Arch Neurol; 2004 Feb; 61(2):209-12. PubMed ID: 14967767
    [TBL] [Abstract][Full Text] [Related]  

  • 4. SCA17 homozygote showing Huntington's disease-like phenotype.
    Toyoshima Y; Yamada M; Onodera O; Shimohata M; Inenaga C; Fujita N; Morita M; Tsuji S; Takahashi H
    Ann Neurol; 2004 Feb; 55(2):281-6. PubMed ID: 14755733
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Spinocerebellar ataxia type 17: extension of phenotype with putaminal rim hyperintensity on magnetic resonance imaging.
    Loy CT; Sweeney MG; Davis MB; Wills AJ; Sawle GV; Lees AJ; Tabrizi SJ
    Mov Disord; 2005 Nov; 20(11):1521-3. PubMed ID: 16037935
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Saccade velocity is controlled by polyglutamine size in spinocerebellar ataxia 2.
    Velázquez-Pérez L; Seifried C; Santos-Falcón N; Abele M; Ziemann U; Almaguer LE; Martínez-Góngora E; Sánchez-Cruz G; Canales N; Pérez-González R; Velázquez-Manresa M; Viebahn B; von Stuckrad-Barre S; Fetter M; Klockgether T; Auburger G
    Ann Neurol; 2004 Sep; 56(3):444-7. PubMed ID: 15349876
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Extrapyramidal signs are a common feature of spinocerebellar ataxia type 17.
    Lee WW; Kim SY; Kim JY; Kim HJ; Park SS; Jeon BS
    Neurology; 2009 Nov; 73(20):1708-9. PubMed ID: 19917997
    [No Abstract]   [Full Text] [Related]  

  • 8. A patient with 41 CAG repeats in SCA17 presenting with parkinsonism and chorea.
    Park H; Jeon BS; Shin JH; Park SH
    Parkinsonism Relat Disord; 2016 Jan; 22():106-7. PubMed ID: 26613966
    [No Abstract]   [Full Text] [Related]  

  • 9. [Advance in research on spinocerebellar ataxia 17].
    Zhang J; Gu W
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Feb; 31(1):44-7. PubMed ID: 24510561
    [TBL] [Abstract][Full Text] [Related]  

  • 10. SCA 17 phenotype with intermediate triplet repeat number.
    Herrema H; Mikkelsen T; Robin A; LeWitt P; Sidiropoulos C
    J Neurol Sci; 2014 Oct; 345(1-2):269-70. PubMed ID: 25091452
    [No Abstract]   [Full Text] [Related]  

  • 11. Eye movement abnormalities in spinocerebellar ataxia type 17 (SCA17).
    Hübner J; Sprenger A; Klein C; Hagenah J; Rambold H; Zühlke C; Kömpf D; Rolfs A; Kimmig H; Helmchen C
    Neurology; 2007 Sep; 69(11):1160-8. PubMed ID: 17846415
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Dominant spinocerebellar ataxias: a molecular approach to classification, diagnosis, pathogenesis and the future.
    Margolis RL
    Expert Rev Mol Diagn; 2003 Nov; 3(6):715-32. PubMed ID: 14628900
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Dominantly inherited ataxias: lessons learned from Machado-Joseph disease/spinocerebellar ataxia type 3.
    Paulson HL
    Semin Neurol; 2007 Apr; 27(2):133-42. PubMed ID: 17390258
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Spinocerebellar ataxia type 8(SCA 8)].
    Izumi Y; Maruyama H; Kawakami H
    No To Shinkei; 2001 Jan; 53(1):34-40. PubMed ID: 11211728
    [No Abstract]   [Full Text] [Related]  

  • 15. Spinocerebellar ataxia type 17 in a patient from an Indian kindred.
    Haubenberger D; Prayer D; Bauer P; Pirker W; Zimprich A; Auff E
    J Neurol; 2006 Nov; 253(11):1513-5. PubMed ID: 16972120
    [No Abstract]   [Full Text] [Related]  

  • 16. Focal dystonia as a presenting sign of spinocerebellar ataxia 17.
    Hagenah JM; Zühlke C; Hellenbroich Y; Heide W; Klein C
    Mov Disord; 2004 Feb; 19(2):217-20. PubMed ID: 14978680
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Polyglutamine repeats of spinocerebellar ataxia 6 impair the cell-death-preventing effect of CaV2.1 Ca2+ channel--loss-of-function cellular model of SCA6.
    Matsuyama Z; Yanagisawa NK; Aoki Y; Black JL; Lennon VA; Mori Y; Imoto K; Inuzuka T
    Neurobiol Dis; 2004 Nov; 17(2):198-204. PubMed ID: 15474358
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Phenotypic homogeneity of the Huntington disease-like presentation in a SCA17 family.
    Schneider SA; van de Warrenburg BP; Hughes TD; Davis M; Sweeney M; Wood N; Quinn NP; Bhatia KP
    Neurology; 2006 Nov; 67(9):1701-3. PubMed ID: 17101913
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Repeat expansion in spinocerebellar ataxia type 17 alleles of the TATA-box binding protein gene: an evolutionary approach.
    Tomiuk J; Bachmann L; Bauer C; Rolfs A; Schöls L; Roos C; Zischler H; Schuler MM; Bruntner S; Riess O; Bauer P
    Eur J Hum Genet; 2007 Jan; 15(1):81-7. PubMed ID: 17033685
    [TBL] [Abstract][Full Text] [Related]  

  • 20. TBP, a polyglutamine tract containing protein, accumulates in Alzheimer's disease.
    Reid SJ; van Roon-Mom WM; Wood PC; Rees MI; Owen MJ; Faull RL; Dragunow M; Snell RG
    Brain Res Mol Brain Res; 2004 Jun; 125(1-2):120-8. PubMed ID: 15193429
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.