Similar articles for PMID: 22700602

Year	Number of Results
2000	3
2001	1
2002	4
2003	5
2004	12
2005	5
2006	2
2007	3
2008	5
2009	1
2010	4
2011	8
2012	6
2013	5
2014	5
2015	7
2016	4
2017	9
2018	4
2019	2
2020	3
2021	7
2022	3
2023	1
2024	0

1

Spinocerebellar ataxia type 2 is associated with Parkinsonism and Lewy body pathology.

Takao M, Aoyama M, Ishikawa K, Sakiyama Y, Yomono H, Saito Y, Kurisaki H, Mihara B, Murayama S. Takao M, et al. BMJ Case Rep. 2011 Apr 1;2011:bcr0120113685. doi: 10.1136/bcr.01.2011.3685. BMJ Case Rep. 2011. PMID: 22700602 Free PMC article.

2

The parkinsonian phenotype of spinocerebellar ataxia type 2.

Lu CS, Wu Chou YH, Kuo PC, Chang HC, Weng YH. Lu CS, et al. Arch Neurol. 2004 Jan;61(1):35-8. doi: 10.1001/archneur.61.1.35. Arch Neurol. 2004. PMID: 14732617

3

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. Schöls L, et al. Brain. 2015 Nov;138(Pt 11):3316-26. doi: 10.1093/brain/awv255. Epub 2015 Sep 11. Brain. 2015. PMID: 26362908

4

Parkinsonism in spinocerebellar ataxia.

Park H, Kim HJ, Jeon BS. Park H, et al. Biomed Res Int. 2015;2015:125273. doi: 10.1155/2015/125273. Epub 2015 Mar 19. Biomed Res Int. 2015. PMID: 25866756 Free PMC article. Review.

5

[Autopsy case of SCA2 with Parkinsonian phenotype].

Yomono HS, Kurisaki H, Hebisawa A, Sakiyama Y, Saito Y, Murayama S. Yomono HS, et al. Rinsho Shinkeigaku. 2010 Mar;50(3):156-62. doi: 10.5692/clinicalneurol.50.156. Rinsho Shinkeigaku. 2010. PMID: 20235484 Japanese.

6

Psychotic-affective symptoms and multiple system atrophy expand phenotypes of spinocerebellar ataxia type 2.

Chen KH, Lin CH, Wu RM. Chen KH, et al. BMJ Case Rep. 2012 Mar 20;2012:bcr1020115061. doi: 10.1136/bcr.10.2011.5061. BMJ Case Rep. 2012. PMID: 22605703 Free PMC article.

7

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. Furtado S, et al. Mov Disord. 2004 Jun;19(6):622-9. doi: 10.1002/mds.20074. Mov Disord. 2004. PMID: 15197699 Review.

8

Spinocerebellar ataxia type 2 with Levodopa-responsive parkinsonism culminating in motor neuron disease.

Infante J, Berciano J, Volpini V, Corral J, Polo JM, Pascual J, Combarros O. Infante J, et al. Mov Disord. 2004 Jul;19(7):848-852. doi: 10.1002/mds.20090. Mov Disord. 2004. PMID: 15254952

9

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. Gwinn-Hardy K, et al. Neurology. 2000 Sep 26;55(6):800-5. doi: 10.1212/wnl.55.6.800. Neurology. 2000. PMID: 10993999

10

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

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