Similar articles for PMID: 9758625

Year	Number of Results
1994	1
1995	6
1996	10
1997	19
1998	8
1999	10
2000	6
2001	8
2002	3
2003	6
2004	7
2005	7
2006	2
2007	7
2008	4
2009	6
2010	5
2011	2
2012	3
2013	3
2014	3
2015	3
2017	2
2018	2
2019	3
2020	2
2021	1
2022	1
2023	2
2024	0

1

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. Takano H, et al. Am J Hum Genet. 1998 Oct;63(4):1060-6. doi: 10.1086/302067. Am J Hum Genet. 1998. PMID: 9758625 Free PMC article.

2

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. Tang B, et al. Arch Neurol. 2000 Apr;57(4):540-4. doi: 10.1001/archneur.57.4.540. Arch Neurol. 2000. PMID: 10768629

3

Analysis of CAG repeats in SCA1, SCA2, SCA3, SCA6, SCA7 and DRPLA loci in spinocerebellar ataxia patients and distribution of CAG repeats at the SCA1, SCA2 and SCA6 loci in nine ethnic populations of eastern India.

Basu P, Chattopadhyay B, Gangopadhaya PK, Mukherjee SC, Sinha KK, Das SK, Roychoudhury S, Majumder PP, Bhattacharyya NP. Basu P, et al. Hum Genet. 2000 Jun;106(6):597-604. doi: 10.1007/s004390000320. Hum Genet. 2000. PMID: 10942107

4

Analysis of SCA1, DRPLA, MJD, SCA2, and SCA6 CAG repeats in 48 Portuguese ataxia families.

Silveira I, Coutinho P, Maciel P, Gaspar C, Hayes S, Dias A, Guimarães J, Loureiro L, Sequeiros J, Rouleau GA. Silveira I, et al. Am J Med Genet. 1998 Mar 28;81(2):134-8. doi: 10.1002/(sici)1096-8628(19980328)81:2<134::aid-ajmg3>3.0.co;2-w. Am J Med Genet. 1998. PMID: 9613852

5

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. Tsai HF, et al. Acta Neurol Scand. 2004 May;109(5):355-60. doi: 10.1046/j.1600-0404.2003.00229.x. Acta Neurol Scand. 2004. PMID: 15080863

6

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. Brusco A, et al. Arch Neurol. 2004 May;61(5):727-33. doi: 10.1001/archneur.61.5.727. Arch Neurol. 2004. PMID: 15148151

7

[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. Tang B, et al. Zhonghua Yi Xue Za Zhi. 1997 Nov;77(11):819-22. Zhonghua Yi Xue Za Zhi. 1997. PMID: 9772474 Chinese.

8

Spinocerebellar ataxias in Spanish patients: genetic analysis of familial and sporadic cases. The Ataxia Study Group.

Pujana MA, Corral J, Gratacòs M, Combarros O, Berciano J, Genís D, Banchs I, Estivill X, Volpini V. Pujana MA, et al. Hum Genet. 1999 Jun;104(6):516-22. doi: 10.1007/s004390050997. Hum Genet. 1999. PMID: 10453742

9

Difference in disease-free survival curve and regional distribution according to subtype of spinocerebellar ataxia: a study of 1,286 Japanese patients.

Maruyama H, Izumi Y, Morino H, Oda M, Toji H, Nakamura S, Kawakami H. Maruyama H, et al. Am J Med Genet. 2002 Jul 8;114(5):578-83. doi: 10.1002/ajmg.10514. Am J Med Genet. 2002. PMID: 12116198

10

Molecular analysis of Spinocerebellar ataxias in Koreans: frequencies and reference ranges of SCA1, SCA2, SCA3, SCA6, and SCA7.

Kim JY, Park SS, Joo SI, Kim JM, Jeon BS. Kim JY, et al. Mol Cells. 2001 Dec 31;12(3):336-41. Mol Cells. 2001. PMID: 11804332 Free article.

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