Song W - Search Results

1

Novel THAP1 gene mutations in patients with primary dystonia from southwest China.

Song W, Chen Y, Huang R, Chen K, Pan P, Yang Y, Shang HF. Song W, et al. J Neurol Sci. 2011 Oct 15;309(1-2):63-7. doi: 10.1016/j.jns.2011.07.023. Epub 2011 Aug 11. J Neurol Sci. 2011. PMID: 21839475

2

Voxelwise meta-analysis of gray matter anomalies in Alzheimer's disease and mild cognitive impairment using anatomic likelihood estimation.

Yang J, Pan P, Song W, Huang R, Li J, Chen K, Gong Q, Zhong J, Shi H, Shang H. Yang J, et al. Among authors: song w. J Neurol Sci. 2012 May 15;316(1-2):21-9. doi: 10.1016/j.jns.2012.02.010. Epub 2012 Mar 3. J Neurol Sci. 2012. PMID: 22385679 Review.

3

GLIS1 rs797906: an increased risk factor for late-onset Parkinson's disease in the Han Chinese population.

Song W, Chen YP, Huang R, Chen K, Pan PL, Li J, Yang Y, Shang HF. Song W, et al. Eur Neurol. 2012;68(2):89-92. doi: 10.1159/000337955. Epub 2012 Jul 3. Eur Neurol. 2012. PMID: 22759478

4

Association analysis of LRP8 SNP rs3820198 and rs5174 with Parkinson's disease in Han Chinese population.

Chen K, Chen YP, Song W, Huang R, Zhao B, Cao B, Yang Y, Satake W, Toda T, Shang HF. Chen K, et al. Among authors: song w. Neurol Res. 2012 Sep;34(7):725-9. doi: 10.1179/1743132812Y.0000000075. Neurol Res. 2012. PMID: 22889673

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: song w. 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: song w. 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: song w. 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

Altered intrinsic brain activity in patients with paroxysmal kinesigenic dyskinesia by PRRT2 mutation: altered brain activity by PRRT2 mutation.

Luo C, Chen Y, Song W, Chen Q, Gong Q, Shang HF. Luo C, et al. Among authors: song w. Neurol Sci. 2013 Nov;34(11):1925-31. doi: 10.1007/s10072-013-1408-7. Epub 2013 Mar 27. Neurol Sci. 2013. PMID: 23532549

9

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: song w. 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

10

GAK rs1564282 and DGKQ rs11248060 increase the risk for Parkinson's disease in a Chinese population.

Chen YP, Song W, Huang R, Chen K, Zhao B, Li J, Yang Y, Shang HF. Chen YP, et al. Among authors: song w. J Clin Neurosci. 2013 Jun;20(6):880-3. doi: 10.1016/j.jocn.2012.07.011. Epub 2013 Apr 23. J Clin Neurosci. 2013. PMID: 23618683

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