Similar articles for PMID: 21880993

Year	Number of Results
1981	1
1993	1
1997	4
1998	2
1999	2
2000	2
2001	5
2002	2
2004	4
2005	2
2007	6
2008	4
2009	4
2010	2
2011	10
2012	9
2013	6
2014	4
2015	6
2016	2
2017	2
2018	3
2019	4
2020	3
2021	1
2022	2
2023	1
2024	0

1

Massive expansion of SCA2 with autonomic dysfunction, retinitis pigmentosa, and infantile spasms.

Paciorkowski AR, Shafrir Y, Hrivnak J, Patterson MC, Tennison MB, Clark HB, Gomez CM. Paciorkowski AR, et al. Neurology. 2011 Sep 13;77(11):1055-60. doi: 10.1212/WNL.0b013e31822e5627. Epub 2011 Aug 31. Neurology. 2011. PMID: 21880993 Free PMC article.

2

Spinocerebellar ataxia type 2 (SCA 2) in an infant with extreme CAG repeat expansion.

Babovic-Vuksanovic D, Snow K, Patterson MC, Michels VV. Babovic-Vuksanovic D, et al. Am J Med Genet. 1998 Oct 12;79(5):383-7. Am J Med Genet. 1998. PMID: 9779806

3

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

4

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. Kim JM, et al. Arch Neurol. 2007 Oct;64(10):1510-8. doi: 10.1001/archneur.64.10.1510. Arch Neurol. 2007. PMID: 17923635

5

ATXN2-AS, a gene antisense to ATXN2, is associated with spinocerebellar ataxia type 2 and amyotrophic lateral sclerosis.

Li PP, Sun X, Xia G, Arbez N, Paul S, Zhu S, Peng HB, Ross CA, Koeppen AH, Margolis RL, Pulst SM, Ashizawa T, Rudnicki DD. Li PP, et al. Ann Neurol. 2016 Oct;80(4):600-15. doi: 10.1002/ana.24761. Ann Neurol. 2016. PMID: 27531668 Free PMC article.

6

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. Wang C, et al. Neurobiol Aging. 2015 Jan;36(1):545.e1-7. doi: 10.1016/j.neurobiolaging.2014.07.039. Epub 2014 Aug 2. Neurobiol Aging. 2015. PMID: 25189117

7

Expansion of the first PolyA tract of ARX causes infantile spasms and status dystonicus.

Guerrini R, Moro F, Kato M, Barkovich AJ, Shiihara T, McShane MA, Hurst J, Loi M, Tohyama J, Norci V, Hayasaka K, Kang UJ, Das S, Dobyns WB. Guerrini R, et al. Neurology. 2007 Jul 31;69(5):427-33. doi: 10.1212/01.wnl.0000266594.16202.c1. Neurology. 2007. PMID: 17664401

8

Germ-line CAG repeat instability causes extreme CAG repeat expansion with infantile-onset spinocerebellar ataxia type 2.

Vinther-Jensen T, Ek J, Duno M, Skovby F, Hjermind LE, Nielsen JE, Nielsen TT. Vinther-Jensen T, et al. Eur J Hum Genet. 2013 Jun;21(6):626-9. doi: 10.1038/ejhg.2012.231. Epub 2012 Oct 10. Eur J Hum Genet. 2013. PMID: 23047744 Free PMC article.

9

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. Laffita-Mesa JM, et al. Hum Genet. 2012 Apr;131(4):625-38. doi: 10.1007/s00439-011-1101-y. Epub 2011 Oct 30. Hum Genet. 2012. PMID: 22037902

10

Common origin of pure and interrupted repeat expansions in spinocerebellar ataxia type 2 (SCA2).

Ramos EM, Martins S, Alonso I, Emmel VE, Saraiva-Pereira ML, Jardim LB, Coutinho P, Sequeiros J, Silveira I. Ramos EM, et al. Am J Med Genet B Neuropsychiatr Genet. 2010 Mar 5;153B(2):524-531. doi: 10.1002/ajmg.b.31013. Am J Med Genet B Neuropsychiatr Genet. 2010. PMID: 19676102

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