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]