BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

163 related articles for article (PubMed ID: 15313853)

  • 21. Cognitive dysfunction, social behavior disorder, cerebellar ataxia, and atypical brain FDG-PET presentation in spinocerebellar ataxia 17: a case report.
    Grassini A; Cermelli A; Roveta F; Zotta M; Lesca A; Marcinnò A; Ferrandes F; Piella E; Boschi S; Lombardo C; Brusco A; Gallone S; Rubino E; Bruni A; Rainero I
    Neurol Sci; 2024 Jun; 45(6):2877-2880. PubMed ID: 38494459
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Spinocerebellar ataxia type 4 (SCA4): Initial pathoanatomical study reveals widespread cerebellar and brainstem degeneration.
    Hellenbroich Y; Gierga K; Reusche E; Schwinger E; Deller T; de Vos RA; Zühlke C; Rüb U
    J Neural Transm (Vienna); 2006 Jul; 113(7):829-43. PubMed ID: 16362839
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Spinocerebellar ataxia type 17: report of a family with reduced penetrance of an unstable Gln49 TBP allele, haplotype analysis supporting a founder effect for unstable alleles and comparative analysis of SCA17 genotypes.
    Zühlke C; Dalski A; Schwinger E; Finckh U
    BMC Med Genet; 2005 Jul; 6():27. PubMed ID: 15989694
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Genetically modified rodent models of SCA17.
    Cui Y; Yang S; Li XJ; Li S
    J Neurosci Res; 2017 Aug; 95(8):1540-1547. PubMed ID: 27859490
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. A novel transgenic rat model for spinocerebellar ataxia type 17 recapitulates neuropathological changes and supplies in vivo imaging biomarkers.
    Kelp A; Koeppen AH; Petrasch-Parwez E; Calaminus C; Bauer C; Portal E; Yu-Taeger L; Pichler B; Bauer P; Riess O; Nguyen HP
    J Neurosci; 2013 May; 33(21):9068-81. PubMed ID: 23699518
    [TBL] [Abstract][Full Text] [Related]  

  • 27. A spinocerebellar ataxia family with expanded alleles in the TATA-binding protein gene and ataxin-3 gene.
    Xu Q; Li Q; Wang J; Jiang H; Shen L; Li X; Tang B
    Int J Neurosci; 2010 Feb; 120(2):159-61. PubMed ID: 20199210
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Severe and rapidly progressing cognitive phenotype in a SCA17-family with only marginally expanded CAG/CAA repeats in the TATA-box binding protein gene: a case report.
    Nielsen TT; Mardosiene S; Løkkegaard A; Stokholm J; Ehrenfels S; Bech S; Friberg L; Nielsen JK; Nielsen JE
    BMC Neurol; 2012 Aug; 12():73. PubMed ID: 22889412
    [TBL] [Abstract][Full Text] [Related]  

  • 29. A small trinucleotide expansion in the TBP gene gives rise to a sporadic case of SCA17 with abnormal putaminal findings on MRI.
    Watanabe M; Monai N; Jackson M; Yamamoto-Watanabe Y; Ikeda Y; Suzuki C; Tomiyama M; Kawarabayashi T; Kimura T; Seino Y; Wakasaya Y; Miki Y; Matsubara E; Shoji M
    Intern Med; 2008; 47(24):2179-82. PubMed ID: 19075547
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Primary degeneration of oculomotor, motor, and somatosensory systems and auditory and visual pathways in spinocerebellar ataxia type 7: A clinicopathological study in a Japanese autopsy case.
    Ouchi H; Ishiguro H; Shibano K; Hara K; Sugawara M; Enomoto K; Miyata H
    Neuropathology; 2023 Apr; 43(2):164-175. PubMed ID: 36168676
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Spinocerebellar ataxia 17 (SCA17) and Huntington's disease-like 4 (HDL4).
    Stevanin G; Brice A
    Cerebellum; 2008; 7(2):170-8. PubMed ID: 18418687
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Characterization of nigrostriatal dysfunction in spinocerebellar ataxia 17.
    Salvatore E; Varrone A; Sansone V; Nolano M; Bruni AC; De Rosa A; Santoro L; Pappatà S; Filla A; De Michele G
    Mov Disord; 2006 Jun; 21(6):872-5. PubMed ID: 16532453
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Spinocerebellar ataxia type 2 (SCA2): identification of early brain degeneration in one monozygous twin in the initial disease stage.
    Hoche F; Balikó L; den Dunnen W; Steinecker K; Bartos L; Sáfrány E; Auburger G; Deller T; Korf HW; Klockgether T; Rüb U; Melegh B
    Cerebellum; 2011 Jun; 10(2):245-53. PubMed ID: 21128038
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Cerebellar cognitive-affective syndrome preceding ataxia associated with complex extrapyramidal features in a Turkish SCA48 family.
    Palvadeau R; Kaya-Güleç ZE; Şimşir G; Vural A; Öztop-Çakmak Ö; Genç G; Aygün MS; Falay O; Başak AN; Ertan S
    Neurogenetics; 2020 Jan; 21(1):51-58. PubMed ID: 31741143
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Neuropathology and Cellular Pathogenesis of Spinocerebellar Ataxia Type 12.
    O'Hearn EE; Hwang HS; Holmes SE; Rudnicki DD; Chung DW; Seixas AI; Cohen RL; Ross CA; Trojanowski JQ; Pletnikova O; Troncoso JC; Margolis RL
    Mov Disord; 2015 Nov; 30(13):1813-1824. PubMed ID: 26340331
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Anticipation and intergenerational repeat instability in spinocerebellar ataxia type 17.
    Rasmussen A; De Biase I; Fragoso-Benítez M; Macías-Flores MA; Yescas P; Ochoa A; Ashizawa T; Alonso ME; Bidichandani SI
    Ann Neurol; 2007 Jun; 61(6):607-10. PubMed ID: 17474109
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. 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]  

  • 39. Bidirectional expression of the SCA8 expansion mutation: one mutation, two genes.
    Ikeda Y; Daughters RS; Ranum LP
    Cerebellum; 2008; 7(2):150-8. PubMed ID: 18418692
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Spinocerebellar ataxia type 7 (SCA7) - correlations between phenotype and genotype in one large Belgian family.
    Martin J; Van Regemorter N; Del-Favero J; Löfgren A; Van Broeckhoven C
    J Neurol Sci; 1999 Sep; 168(1):37-46. PubMed ID: 10500272
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.