Similar articles for PMID: 19811945

Year	Number of Results
1993	1
1995	3
1997	1
1998	3
1999	3
2000	1
2001	5
2003	1
2004	2
2005	1
2006	3
2007	3
2008	5
2009	9
2010	11
2011	12
2012	14
2013	20
2014	14
2015	11
2016	2
2017	4
2018	5
2019	9
2020	10
2021	17
2022	19
2023	11
2024	0

1

Caring for Machado-Joseph disease: current understanding and how to help patients.

D'Abreu A, França MC Jr, Paulson HL, Lopes-Cendes I. D'Abreu A, et al. Parkinsonism Relat Disord. 2010 Jan;16(1):2-7. doi: 10.1016/j.parkreldis.2009.08.012. Epub 2009 Oct 6. Parkinsonism Relat Disord. 2010. PMID: 19811945 Free PMC article. Review.

2

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. Bettencourt C, et al. BMC Neurol. 2011 Oct 24;11:131. doi: 10.1186/1471-2377-11-131. BMC Neurol. 2011. PMID: 22023810 Free PMC article.

3

A new humanized ataxin-3 knock-in mouse model combines the genetic features, pathogenesis of neurons and glia and late disease onset of SCA3/MJD.

Switonski PM, Szlachcic WJ, Krzyzosiak WJ, Figiel M. Switonski PM, et al. Neurobiol Dis. 2015 Jan;73:174-88. doi: 10.1016/j.nbd.2014.09.020. Epub 2014 Oct 7. Neurobiol Dis. 2015. PMID: 25301414 Free article.

4

Machado-Joseph disease/spinocerebellar ataxia type 3.

Paulson H. Paulson H. Handb Clin Neurol. 2012;103:437-49. doi: 10.1016/B978-0-444-51892-7.00027-9. Handb Clin Neurol. 2012. PMID: 21827905 Free PMC article. Review.

5

[Polyglutamine-expanded ataxin-3 is degraded by autophagy].

Xiao H, Tang J, Hu Z, Tan J, Tang B, Jiang Z. Xiao H, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2010 Feb;27(1):23-8. doi: 10.3760/cma.j.issn.1003-9406.2010.01.005. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2010. PMID: 20140862 Chinese.

6

[Recent advances in molecular genetics of spinocerebellar ataxia type 3/Machado-Joseph disease].

Jia D, Jiang H, Tang B. Jia D, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008 Dec;25(6):660-2. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008. PMID: 19065526 Review. Chinese.

7

APOE ε2 allele may decrease the age at onset in patients with spinocerebellar ataxia type 3 or Machado-Joseph disease from the Chinese Han population.

Peng H, Wang C, Chen Z, Sun Z, Jiao B, Li K, Huang F, Hou X, Wang J, Shen L, Xia K, Tang B, Jiang H. Peng H, et al. Neurobiol Aging. 2014 Sep;35(9):2179.e15-8. doi: 10.1016/j.neurobiolaging.2014.03.020. Epub 2014 Mar 22. Neurobiol Aging. 2014. PMID: 24746364

8

Inactivation of PNKP by mutant ATXN3 triggers apoptosis by activating the DNA damage-response pathway in SCA3.

Gao R, Liu Y, Silva-Fernandes A, Fang X, Paulucci-Holthauzen A, Chatterjee A, Zhang HL, Matsuura T, Choudhary S, Ashizawa T, Koeppen AH, Maciel P, Hazra TK, Sarkar PS. Gao R, et al. PLoS Genet. 2015 Jan 15;11(1):e1004834. doi: 10.1371/journal.pgen.1004834. eCollection 2015 Jan. PLoS Genet. 2015. PMID: 25590633 Free PMC article.

9

Six cases of SCA3/MJD patients that mimic hereditary spastic paraplegia in clinic.

Wang YG, Du J, Wang JL, Chen J, Chen C, Luo YY, Xiao ZQ, Jiang H, Yan XX, Xia K, Pan Q, Tang BS, Shen L. Wang YG, et al. J Neurol Sci. 2009 Oct 15;285(1-2):121-4. doi: 10.1016/j.jns.2009.06.027. Epub 2009 Jul 15. J Neurol Sci. 2009. PMID: 19608203

10

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

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