Chen X - Search Results

1

Disease duration-related differences in non-motor symptoms: a study of 616 Chinese Parkinson's disease patients.

Guo X, Song W, Chen K, Chen X, Zheng Z, Cao B, Huang R, Zhao B, Wu Y, Shang HF. Guo X, et al. Among authors: chen k, chen x. J Neurol Sci. 2013 Jul 15;330(1-2):32-7. doi: 10.1016/j.jns.2013.03.022. Epub 2013 Apr 17. J Neurol Sci. 2013. PMID: 23601697

2

A novel mutation of the epsilon-sarcoglycan gene in a Chinese family with myoclonus-dystonia syndrome.

Chen XP, Zhang YW, Zhang SS, Chen Q, Burgunder JM, Wu SH, Yang Y, Luo ZM, Shang HF. Chen XP, et al. Mov Disord. 2008 Jul 30;23(10):1472-5. doi: 10.1002/mds.22008. Mov Disord. 2008. PMID: 18581468

3

RNA interference-mediated inhibition of wild-type Torsin A expression increases apoptosis caused by oxidative stress in cultured cells.

Chen XP, Hu XH, Wu SH, Zhang YW, Xiao B, Shang HF. Chen XP, et al. Neurochem Res. 2010 Aug;35(8):1214-23. doi: 10.1007/s11064-010-0177-4. Epub 2010 May 9. Neurochem Res. 2010. PMID: 20455020

4

Patterns of spontaneous brain activity in amyotrophic lateral sclerosis: a resting-state FMRI study.

Luo C, Chen Q, Huang R, Chen X, Chen K, Huang X, Tang H, Gong Q, Shang HF. Luo C, et al. Among authors: chen k, chen q, chen x. PLoS One. 2012;7(9):e45470. doi: 10.1371/journal.pone.0045470. Epub 2012 Sep 20. PLoS One. 2012. PMID: 23029031 Free PMC article.

5

Association of rs1182 polymorphism of the DYT1 gene with primary dystonia in Chinese population.

Chen Y, Chen K, Burgunder JM, Song W, Huang R, Zhao B, Cao B, Chen X, Jiang Y, Shang HF. Chen Y, et al. Among authors: chen k, chen x. J Neurol Sci. 2012 Dec 15;323(1-2):228-31. doi: 10.1016/j.jns.2012.09.025. Epub 2012 Oct 9. J Neurol Sci. 2012. PMID: 23058565

6

VPS35 Asp620Asn and EIF4G1 Arg1205His mutations are rare in Parkinson disease from southwest China.

Chen Y, Chen K, Song W, Chen X, Cao B, Huang R, Zhao B, Guo X, Burgunder J, Li J, Shang HF. Chen Y, et al. Among authors: chen k, chen x. Neurobiol Aging. 2013 Jun;34(6):1709.e7-8. doi: 10.1016/j.neurobiolaging.2012.11.003. Epub 2012 Dec 20. Neurobiol Aging. 2013. PMID: 23261770

7

PFN1 mutations are rare in Han Chinese populations with amyotrophic lateral sclerosis.

Chen Y, Zheng ZZ, Huang R, Chen K, Song W, Zhao B, Chen X, Yang Y, Yuan L, Shang HF. Chen Y, et al. Among authors: chen k, chen x. Neurobiol Aging. 2013 Jul;34(7):1922.e1-5. doi: 10.1016/j.neurobiolaging.2013.01.013. Epub 2013 Feb 19. Neurobiol Aging. 2013. PMID: 23428184

8

PRRT2 mutation screening in patients with paroxysmal kinesigenic dyskinesia from Southwest China.

Chen YP, Song W, Yang J, Zheng ZZ, Huang R, Chen K, Zhao B, Chen XP, Burgunder JM, Shang HF. Chen YP, et al. Among authors: chen k, chen xp. Eur J Neurol. 2014;21(1):174-6. doi: 10.1111/ene.12122. Epub 2013 Mar 16. Eur J Neurol. 2014. PMID: 23496026

9

Gender and onset age-related features of non-motor symptoms of patients with Parkinson's disease--a study from Southwest China.

Guo X, Song W, Chen K, Chen X, Zheng Z, Cao B, Huang R, Zhao B, Wu Y, Shang HF. Guo X, et al. Among authors: chen k, chen x. Parkinsonism Relat Disord. 2013 Nov;19(11):961-5. doi: 10.1016/j.parkreldis.2013.06.009. Epub 2013 Jul 10. Parkinsonism Relat Disord. 2013. PMID: 23849500

10

Altered regional spontaneous neuronal activity in blepharospasm: a resting state fMRI study.

Yang J, Luo C, Song W, Chen Q, Chen K, Chen X, Huang X, Gong Q, Shang H. Yang J, et al. Among authors: chen k, chen q, chen x. J Neurol. 2013 Nov;260(11):2754-60. doi: 10.1007/s00415-013-7042-8. Epub 2013 Jul 31. J Neurol. 2013. PMID: 23900755

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