BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

151 related articles for article (PubMed ID: 21307863)

  • 1. Genetic and clinical analysis in a Chinese parkinsonism-predominant spinocerebellar ataxia type 2 family.
    Sun H; Satake W; Zhang C; Nagai Y; Tian Y; Fu S; Yu J; Qian Y; Qian Y; Chu J; Toda T
    J Hum Genet; 2011 Apr; 56(4):330-4. PubMed ID: 21307863
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Linkage analysis and whole-exome sequencing exclude extra mutations responsible for the parkinsonian phenotype of spinocerebellar ataxia-2.
    Wang C; Xu Y; Feng X; Ma J; Xie S; Zhang Y; Tang BS; Chan P
    Neurobiol Aging; 2015 Jan; 36(1):545.e1-7. PubMed ID: 25189117
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Are interrupted SCA2 CAG repeat expansions responsible for parkinsonism?
    Charles P; Camuzat A; Benammar N; Sellal F; Destée A; Bonnet AM; Lesage S; Le Ber I; Stevanin G; Dürr A; Brice A;
    Neurology; 2007 Nov; 69(21):1970-5. PubMed ID: 17568014
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Three spinocerebellar ataxia type 2 siblings with ataxia, parkinsonism, and motor neuronopathy.
    Nishikawa N; Nagai M; Tsujii T; Tanabe N; Takashima H; Nomoto M
    Intern Med; 2011; 50(13):1429-32. PubMed ID: 21720065
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Epigenetics DNA methylation in the core ataxin-2 gene promoter: novel physiological and pathological implications.
    Laffita-Mesa JM; Bauer PO; Kourí V; Peña Serrano L; Roskams J; Almaguer Gotay D; Montes Brown JC; Martínez Rodríguez PA; González-Zaldívar Y; Almaguer Mederos L; Cuello-Almarales D; Aguiar Santiago J
    Hum Genet; 2012 Apr; 131(4):625-38. PubMed ID: 22037902
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Profile of families with parkinsonism-predominant spinocerebellar ataxia type 2 (SCA2).
    Furtado S; Payami H; Lockhart PJ; Hanson M; Nutt JG; Singleton AA; Singleton A; Bower J; Utti RJ; Bird TD; de la Fuente-Fernandez R; Tsuboi Y; Klimek ML; Suchowersky O; Hardy J; Calne DB; Wszolek ZK; Farrer M; Gwinn-Hardy K; Stoessl AJ
    Mov Disord; 2004 Jun; 19(6):622-9. PubMed ID: 15197699
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Psychotic-affective symptoms and multiple system atrophy expand phenotypes of spinocerebellar ataxia type 2.
    Chen KH; Lin CH; Wu RM
    BMJ Case Rep; 2012 Mar; 2012():. PubMed ID: 22605703
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. SCA2 family presenting as typical Parkinson's disease: 34 year follow up.
    Kim YE; Jeon B; Farrer MJ; Scott E; Guella I; Park SS; Kim JM; Park HY; Kim A; Son YD; Cho ZH
    Parkinsonism Relat Disord; 2017 Jul; 40():69-72. PubMed ID: 28462804
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Autopsy case of SCA2 with Parkinsonian phenotype].
    Yomono HS; Kurisaki H; Hebisawa A; Sakiyama Y; Saito Y; Murayama S
    Rinsho Shinkeigaku; 2010 Mar; 50(3):156-62. PubMed ID: 20235484
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genetic profile and clinical characteristics of Chinese patients with spinocerebellar ataxia type 2: A multicenter experience over 10 years.
    Yang L; Dong Y; Ma Y; Ni W; Wu ZY
    Eur J Neurol; 2021 Mar; 28(3):955-964. PubMed ID: 33070405
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mapping of autosomal dominant cerebellar ataxia without the pathogenic PPP2R2B mutation to the locus for spinocerebellar ataxia 12.
    Sato K; Yabe I; Fukuda Y; Soma H; Nakahara Y; Tsuji S; Sasaki H
    Arch Neurol; 2010 Oct; 67(10):1257-62. PubMed ID: 20937954
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Spinocerebellar ataxia type 2 with parkinsonism in ethnic Chinese.
    Gwinn-Hardy K; Chen JY; Liu HC; Liu TY; Boss M; Seltzer W; Adam A; Singleton A; Koroshetz W; Waters C; Hardy J; Farrer M
    Neurology; 2000 Sep; 55(6):800-5. PubMed ID: 10993999
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Prevalence of spinocerebellar ataxia type 2 mutation among Italian Parkinsonian patients.
    Modoni A; Contarino MF; Bentivoglio AR; Tabolacci E; Santoro M; Calcagni ML; Tonali PA; Neri G; Silvestri G
    Mov Disord; 2007 Feb; 22(3):324-7. PubMed ID: 17149720
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 8.