These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
319 related articles for article (PubMed ID: 19953482)
21. Spinocerebellar ataxia type 1 in China: molecular analysis and genotype-phenotype correlation in 5 families. Zhou YX; Qiao WH; Gu WH; Xie H; Tang BS; Zhou LS; Yang BX; Takiyama Y; Tsuji S; He HY; Deng CX; Goldfarb LG; Wang GX Arch Neurol; 2001 May; 58(5):789-94. PubMed ID: 11346374 [TBL] [Abstract][Full Text] [Related]
22. 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]
23. [Studies on the CTA/CTG trinucleotide repeats of ATXN8OS gene in Chinese Hans]. Wang J; Zhang S; Xu Q; Li X; Song X; Jiang H; Shen L; Yan X; Pan Q; Xia K; Tang B Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Oct; 25(5):511-4. PubMed ID: 18841561 [TBL] [Abstract][Full Text] [Related]
24. Spinocerebellar ataxias in Brazil--frequencies and modulating effects of related genes. de Castilhos RM; Furtado GV; Gheno TC; Schaeffer P; Russo A; Barsottini O; Pedroso JL; Salarini DZ; Vargas FR; de Lima MA; Godeiro C; Santana-da-Silva LC; Toralles MB; Santos S; van der Linden H; Wanderley HY; de Medeiros PF; Pereira ET; Ribeiro E; Saraiva-Pereira ML; Jardim LB; Cerebellum; 2014 Feb; 13(1):17-28. PubMed ID: 23943520 [TBL] [Abstract][Full Text] [Related]
26. [Gene diagnosis and CAG repeat analysis of spinocerebellar ataxia cases of Guangxi region]. Tan JQ; Wang P; Hu QP; Li SF; Shu W; Ma J; Fang L; Hua R; Ding Y; Yuan ZG Yi Chuan; 2009 Jun; 31(6):605-10. PubMed ID: 19586860 [TBL] [Abstract][Full Text] [Related]
27. [The clinical features and gene mutation analysis in a pedigree of spinocerebellar ataxia type 7]. Yin XZ; Zhang BR; Wu DW; Tian J; Zhang H Yi Chuan; 2007 Jun; 29(6):688-92. PubMed ID: 17650485 [TBL] [Abstract][Full Text] [Related]
28. [Copy number variation of trinucleotide repeat in dynamic mutation sites of autosomal dominant cerebellar ataxias related genes]. Chen P; Ma M; Shang H; Su D; Zhang S; Yang Y Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Dec; 26(6):626-33. PubMed ID: 19953483 [TBL] [Abstract][Full Text] [Related]
29. Close associations between prevalences of dominantly inherited spinocerebellar ataxias with CAG-repeat expansions and frequencies of large normal CAG alleles in Japanese and Caucasian populations. Takano H; Cancel G; Ikeuchi T; Lorenzetti D; Mawad R; Stevanin G; Didierjean O; Dürr A; Oyake M; Shimohata T; Sasaki R; Koide R; Igarashi S; Hayashi S; Takiyama Y; Nishizawa M; Tanaka H; Zoghbi H; Brice A; Tsuji S Am J Hum Genet; 1998 Oct; 63(4):1060-6. PubMed ID: 9758625 [TBL] [Abstract][Full Text] [Related]
30. Frequency analysis of autosomal dominant cerebellar ataxias in Taiwanese patients and clinical and molecular characterization of spinocerebellar ataxia type 6. Soong B W; Lu Y C; Choo K B; Lee H Y Arch Neurol; 2001 Jul; 58(7):1105-9. PubMed ID: 11448300 [TBL] [Abstract][Full Text] [Related]
31. Genetic etiology of a Chinese ataxia cohort: Expanding the mutational spectrum of hereditary ataxias. Wan N; Chen Z; Wan L; Yuan H; Tang Z; Liu M; Peng Y; Peng L; Lei L; Xie Y; Deng Q; Wang S; Wang C; Peng H; Hou X; Shi Y; Long Z; Qiu R; Xia K; Tang B; Jiang H Parkinsonism Relat Disord; 2021 Aug; 89():120-127. PubMed ID: 34284285 [TBL] [Abstract][Full Text] [Related]
32. Spinocerebellar ataxia type 6 in Mainland China: molecular and clinical features in four families. Jiang H; Tang B; Xia K; Zhou Y; Xu B; Zhao G; Li H; Shen L; Pan Q; Cai F J Neurol Sci; 2005 Sep; 236(1-2):25-9. PubMed ID: 15979648 [TBL] [Abstract][Full Text] [Related]
33. Analysis of spinocerebellar ataxias due to expanded triplet repeats in Greek patients with cerebellar ataxia. Koutsis G; Pemble S; Sweeney MG; Paudel R; Wood NW; Panas M; Kladi A; Houlden H J Neurol Sci; 2012 Jul; 318(1-2):178-80. PubMed ID: 22520093 [TBL] [Abstract][Full Text] [Related]
34. 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]
35. Spinocerebellar ataxias types 1, 2 and 3: age adjusted clinical severity of disease at presentation correlates with size of CAG repeat lengths. Netravathi M; Pal PK; Purushottam M; Thennarasu K; Mukherjee M; Jain S J Neurol Sci; 2009 Feb; 277(1-2):83-6. PubMed ID: 19049837 [TBL] [Abstract][Full Text] [Related]
36. Analysis of CAG repeats in five SCA loci in Mexican population: epidemiological evidence of a SCA7 founder effect. Magaña JJ; Tapia-Guerrero YS; Velázquez-Pérez L; Cerecedo-Zapata CM; Maldonado-Rodríguez M; Jano-Ito JS; Leyva-García N; González-Piña R; Martínez-Cruz E; Hernández-Hernández O; Cisneros B Clin Genet; 2014 Feb; 85(2):159-65. PubMed ID: 23368522 [TBL] [Abstract][Full Text] [Related]
37. Identification of 46 CAG repeats within PPP2R2B as probably the shortest pathogenic allele for SCA12. Dong Y; Wu JJ; Wu ZY Parkinsonism Relat Disord; 2015 Apr; 21(4):398-401. PubMed ID: 25634432 [TBL] [Abstract][Full Text] [Related]
39. [Clinical characteristics and molecular biology of hereditary spinocerebellar ataxia type 7: study of 3 Chinese families]. Song XW; Tang BS; Jiang H; Shen L; Yang Q; Liao SS; Li QH; Liang XC; Tang JG Zhonghua Yi Xue Za Zhi; 2006 Jul; 86(25):1755-8. PubMed ID: 17054842 [TBL] [Abstract][Full Text] [Related]
40. Identification of five spinocerebellar ataxia type 2 pedigrees in patients with autosomal dominant cerebellar ataxia in Taiwan. Hsieh M; Li SY; Tsai CJ; Chen YY; Liu CS; Chang CY; Ro LS; Chen DF; Chen SS; Li C Acta Neurol Scand; 1999 Sep; 100(3):189-94. PubMed ID: 10478584 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]