BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

368 related articles for article (PubMed ID: 26004545)

  • 1. Clinical characteristics of combined cases of spinocerebellar ataxia types 6 and 31.
    Ohmori H; Hara A; Ishikawa K; Mizusawa H; Ando Y
    J Neurogenet; 2015; 29(2-3):80-4. PubMed ID: 26004545
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Clinical features and MRI findings in spinocerebellar ataxia type 31 (SCA31) comparing with spinocerebellar ataxia type 6 (SCA6)].
    Sakakibara S; Aiba I; Saito Y; Inukai A; Ishikawa K; Mizusawa H
    Rinsho Shinkeigaku; 2014; 54(6):473-9. PubMed ID: 24990830
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Spinocerebellar ataxia type 6 and episodic ataxia type 2 in a Korean family.
    Koh SH; Kim HT; Kim SH; Lee GY; Kim J; Kim MH
    J Korean Med Sci; 2001 Dec; 16(6):809-13. PubMed ID: 11748369
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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; 57(3):349-54. PubMed ID: 15732118
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A neuropathological study at autopsy of early onset spinocerebellar ataxia 6.
    Wang X; Wang H; Xia Y; Jiang H; Shen L; Wang S; Shen R; Huang L; Wang J; Xu Q; Li X; Luo X; Tang B
    J Clin Neurosci; 2010 Jun; 17(6):751-5. PubMed ID: 20359894
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Rare frequency of downbeat positioning nystagmus in spinocerebellar ataxia type 31.
    Yabe I; Matsushima M; Yoshida K; Ishikawa K; Shirai S; Takahashi I; Sasaki H
    J Neurol Sci; 2015 Mar; 350(1-2):90-2. PubMed ID: 25684342
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Meiotic CAG repeat instability in spinocerebellar ataxia type 6: maternally transmitted elongation in a presumed sporadic case.
    Lindquist SG; Nørremølle A; Hjermind LE; Hasholt L; Nielsen JE
    J Neurol Sci; 2006 Feb; 241(1-2):95-8. PubMed ID: 16310805
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Identification of a new family of spinocerebellar ataxia type 14 in the Japanese spinocerebellar ataxia population by the screening of PRKCG exon 4.
    Hiramoto K; Kawakami H; Inoue K; Seki T; Maruyama H; Morino H; Matsumoto M; Kurisu K; Sakai N
    Mov Disord; 2006 Sep; 21(9):1355-60. PubMed ID: 16763984
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Spinocerebellar ataxia type 6.
    Solodkin A; Gomez CM
    Handb Clin Neurol; 2012; 103():461-73. PubMed ID: 21827907
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Episodic ataxia and SCA6 within the same family due to the D302N CACNA1A gene mutation.
    Pradotto L; Mencarelli M; Bigoni M; Milesi A; Di Blasio A; Mauro A
    J Neurol Sci; 2016 Dec; 371():81-84. PubMed ID: 27871455
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Pontine atrophy in spinocerebellar ataxia type 6.
    Sugawara M; Toyoshima I; Wada C; Kato K; Ishikawa K; Hirota K; Ishiguro H; Kagaya H; Hirata Y; Imota T; Ogasawara M; Masamune O
    Eur Neurol; 2000; 43(1):17-22. PubMed ID: 10601803
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Visualization, quantification and correlation of brain atrophy with clinical symptoms in spinocerebellar ataxia types 1, 3 and 6.
    Schulz JB; Borkert J; Wolf S; Schmitz-Hübsch T; Rakowicz M; Mariotti C; Schöls L; Timmann D; van de Warrenburg B; Dürr A; Pandolfo M; Kang JS; Mandly AG; Nägele T; Grisoli M; Boguslawska R; Bauer P; Klockgether T; Hauser TK
    Neuroimage; 2010 Jan; 49(1):158-68. PubMed ID: 19631275
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genotype-specific patterns of atrophy progression are more sensitive than clinical decline in SCA1, SCA3 and SCA6.
    Reetz K; Costa AS; Mirzazade S; Lehmann A; Juzek A; Rakowicz M; Boguslawska R; Schöls L; Linnemann C; Mariotti C; Grisoli M; Dürr A; van de Warrenburg BP; Timmann D; Pandolfo M; Bauer P; Jacobi H; Hauser TK; Klockgether T; Schulz JB;
    Brain; 2013 Mar; 136(Pt 3):905-17. PubMed ID: 23423669
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Autopsy case of spinocerebellar ataxia type 31 with severe dementia at the terminal stage.
    Adachi T; Kitayama M; Nakano T; Adachi Y; Kato S; Nakashima K
    Neuropathology; 2015 Jun; 35(3):273-9. PubMed ID: 25495291
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Spinocerebellar ataxia type 31 exists in northeast China.
    Ouyang Y; He Z; Li L; Qin X; Zhao Y; Yuan L
    J Neurol Sci; 2012 May; 316(1-2):164-7. PubMed ID: 22353852
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A novel missense mutation in CACNA1A evaluated by in silico protein modeling is associated with non-episodic spinocerebellar ataxia with slow progression.
    Bürk K; Kaiser FJ; Tennstedt S; Schöls L; Kreuz FR; Wieland T; Strom TM; Büttner T; Hollstein R; Braunholz D; Plaschke J; Gillessen-Kaesbach G; Zühlke C
    Eur J Med Genet; 2014 Apr; 57(5):207-11. PubMed ID: 24486772
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Spinocerebellar ataxia type 6 and episodic ataxia type 2: differences and similarities between two allelic disorders.
    Mantuano E; Veneziano L; Jodice C; Frontali M
    Cytogenet Genome Res; 2003; 100(1-4):147-53. PubMed ID: 14526175
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mutation in the catalytic domain of protein kinase C gamma and extension of the phenotype associated with spinocerebellar ataxia type 14.
    Stevanin G; Hahn V; Lohmann E; Bouslam N; Gouttard M; Soumphonphakdy C; Welter ML; Ollagnon-Roman E; Lemainque A; Ruberg M; Brice A; Durr A
    Arch Neurol; 2004 Aug; 61(8):1242-8. PubMed ID: 15313841
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Gene dosage effect in spinocerebellar ataxia type 6 homozygotes: A clinical and neuropathological study.
    Soga K; Ishikawa K; Furuya T; Iida T; Yamada T; Ando N; Ota K; Kanno-Okada H; Tanaka S; Shintaku M; Eishi Y; Mizusawa H; Yokota T
    J Neurol Sci; 2017 Feb; 373():321-328. PubMed ID: 28131213
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Rapid Onset of Motor Deficits in a Mouse Model of Spinocerebellar Ataxia Type 6 Precedes Late Cerebellar Degeneration.
    Jayabal S; Ljungberg L; Erwes T; Cormier A; Quilez S; El Jaouhari S; Watt AJ
    eNeuro; 2015; 2(6):. PubMed ID: 26730403
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 19.