BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

142 related articles for article (PubMed ID: 21334959)

  • 1. Relative contribution of SCA2, SCA3 and SCA17 in Korean patients with parkinsonism and ataxia.
    Yun JY; Lee WW; Kim HJ; Kim JS; Kim JM; Kim HJ; Kim SY; Kim JY; Park SS; Kim YK; Kim SE; Jeon BS
    Parkinsonism Relat Disord; 2011 Jun; 17(5):338-42. PubMed ID: 21334959
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Lack of mutations in spinocerebellar ataxia type 2 and 3 genes in a Taiwanese (ethnic Chinese) cohort of familial and early-onset parkinsonism.
    Lin CH; Hwu WL; Chiang SC; Tai CH; Wu RM
    Am J Med Genet B Neuropsychiatr Genet; 2007 Jun; 144B(4):434-8. PubMed ID: 17440947
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genetic analysis of SCA2, 3 and 17 in idiopathic Parkinson's disease.
    Lim SW; Zhao Y; Chua E; Law HY; Yuen Y; Pavanni R; Wong MC; Ng IS; Yoon CS; Puong KY; Lim SH; Tan EK
    Neurosci Lett; 2006 Jul; 403(1-2):11-4. PubMed ID: 16687213
    [TBL] [Abstract][Full Text] [Related]  

  • 4. No parkinsonism in SCA2 and SCA3 despite severe neurodegeneration of the dopaminergic substantia nigra.
    Schöls L; Reimold M; Seidel K; Globas C; Brockmann K; Hauser TK; Auburger G; Bürk K; den Dunnen W; Reischl G; Korf HW; Brunt ER; Rüb U
    Brain; 2015 Nov; 138(Pt 11):3316-26. PubMed ID: 26362908
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Heterogeneous nonataxic phenotypes of spinocerebellar ataxia in a Taiwanese population.
    Chen SJ; Lee NC; Chien YH; Hwu WL; Lin CH
    Brain Behav; 2019 Oct; 9(10):e01414. PubMed ID: 31523939
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Spinocerebellar ataxia type 17 mutation as a causative and susceptibility gene in parkinsonism.
    Kim JY; Kim SY; Kim JM; Kim YK; Yoon KY; Kim JY; Lee BC; Kim JS; Paek SH; Park SS; Kim SE; Jeon BS
    Neurology; 2009 Apr; 72(16):1385-9. PubMed ID: 19380697
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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; 44(3):238-45. PubMed ID: 20625959
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The prevalence and wide clinical spectrum of the spinocerebellar ataxia type 2 trinucleotide repeat in patients with autosomal dominant cerebellar ataxia.
    Geschwind DH; Perlman S; Figueroa CP; Treiman LJ; Pulst SM
    Am J Hum Genet; 1997 Apr; 60(4):842-50. PubMed ID: 9106530
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Importance of low-range CAG expansion and CAA interruption in SCA2 Parkinsonism.
    Kim JM; Hong S; Kim GP; Choi YJ; Kim YK; Park SS; Kim SE; Jeon BS
    Arch Neurol; 2007 Oct; 64(10):1510-8. PubMed ID: 17923635
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Intrafamilial variability of Parkinson phenotype in SCAs: novel cases due to SCA2 and SCA3 expansions.
    Socal MP; Emmel VE; Rieder CR; Hilbig A; Saraiva-Pereira ML; Jardim LB
    Parkinsonism Relat Disord; 2009 Jun; 15(5):374-8. PubMed ID: 18990604
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The parkinsonian phenotype of spinocerebellar ataxia type 3 in a Taiwanese family.
    Lu CS; Chang HC; Kuo PC; Liu YL; Wu WS; Weng YH; Yen TC; Chou YH
    Parkinsonism Relat Disord; 2004 Aug; 10(6):369-73. PubMed ID: 15261879
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genetic analysis of SCA 2 and 3 repeat expansions in essential tremor and atypical Parkinsonism.
    Tan EK; Tong J; Pavanni R; Wong MC; Zhao Y
    Mov Disord; 2007 Oct; 22(13):1971-4. PubMed ID: 17712857
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [SCA1, SCA2, MJD/SCA3 (CAG)n mutation detection and analysis in patients with hereditary spinocerebellar ataxia from Chinese families].
    Tang B; Wang D; Xia J
    Zhonghua Yi Xue Za Zhi; 1997 Nov; 77(11):819-22. PubMed ID: 9772474
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Parkinsonian phenotype in Machado-Joseph disease (MJD/SCA3): a two-case report.
    Bettencourt C; Santos C; Coutinho P; Rizzu P; Vasconcelos J; Kay T; Cymbron T; Raposo M; Heutink P; Lima M
    BMC Neurol; 2011 Oct; 11():131. PubMed ID: 22023810
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Analysis of SCA2 and SCA3/MJD repeats in Parkinson's disease in mainland China: genetic, clinical, and positron emission tomography findings.
    Wang JL; Xiao B; Cui XX; Guo JF; Lei LF; Song XW; Shen L; Jiang H; Yan XX; Pan Q; Long ZG; Xia K; Tang BS
    Mov Disord; 2009 Oct; 24(13):2007-11. PubMed ID: 19672991
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Analysis of trinucleotide repeats in different SCA loci in spinocerebellar ataxia patients and in normal population of Taiwan.
    Tsai HF; Liu CS; Leu TM; Wen FC; Lin SJ; Liu CC; Yang DK; Li C; Hsieh M
    Acta Neurol Scand; 2004 May; 109(5):355-60. PubMed ID: 15080863
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Parkinsonism in spinocerebellar ataxia.
    Park H; Kim HJ; Jeon BS
    Biomed Res Int; 2015; 2015():125273. PubMed ID: 25866756
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Frequency of different subtypes of spinocerebellar ataxia in the Han nationality of Hunan province in China].
    Song XW; Tang BS; Jiang H; Shen L; Yang Q; Liao SS; Li QH; Tang JG
    Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2006 Oct; 31(5):702-5. PubMed ID: 17062934
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.