Wang N - Search Results

1

Mitochondrial DNA Haplogroups and the Risk of Sporadic Parkinson's Disease in Han Chinese.

Chen YF, Chen WJ, Lin XZ, Zhang QJ, Cai JP, Liou CW, Wang N. Chen YF, et al. Among authors: wang n. Chin Med J (Engl). 2015 Jul 5;128(13):1748-54. doi: 10.4103/0366-6999.159348. Chin Med J (Engl). 2015. PMID: 26112715 Free PMC article.

2

[Study on EcoR I fragment polymorphism of the subtelomeric domains within 4q35 and 10q26 with pulsed field gel electrophoresis in the Chinese population].

Wu ZY, Wang ZQ, Wang N, Lin MT, Murong SX. Wu ZY, et al. Among authors: wang n, wang zq. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004 Dec;21(6):552-6. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004. PMID: 15583980 Chinese.

3

Rapid diagnosis of spinal muscular atrophy using denaturing high-performance liquid chromatography.

Chen WJ, Wu ZY, Wang N, Lin MT, Mu-Rong SX. Chen WJ, et al. Among authors: wang n. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Jun;22(3):291-3. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005. PMID: 15952118

4

[Prevalence of CYP2C19 polymorphisms involved in clopidogrel metabolism in Fujian Han population].

Wei W, Fang L, Wang N, Zhang T, Zeng JB, Lin MT. Wei W, et al. Among authors: wang n. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012 Aug;29(4):420-5. doi: 10.3760/cma.j.issn.1003-9406.2012.04.009. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012. PMID: 22875498 Chinese.

5

Modification of phenotype by SMN2 copy numbers in two Chinese families with SMN1 deletion in two continuous generations.

Chen WJ, He J, Zhang QJ, Lin QF, Chen YF, Lin XZ, Lin MT, Murong SX, Wang N. Chen WJ, et al. Among authors: wang n. Clin Chim Acta. 2012 Nov 20;413(23-24):1855-60. doi: 10.1016/j.cca.2012.07.020. Epub 2012 Aug 4. Clin Chim Acta. 2012. PMID: 22884440

6

Molecular analysis of SMN1, SMN2, NAIP, GTF2H2, and H4F5 genes in 157 Chinese patients with spinal muscular atrophy.

He J, Zhang QJ, Lin QF, Chen YF, Lin XZ, Lin MT, Murong SX, Wang N, Chen WJ. He J, et al. Among authors: wang n. Gene. 2013 Apr 15;518(2):325-9. doi: 10.1016/j.gene.2012.12.109. Epub 2013 Jan 23. Gene. 2013. PMID: 23352792

7

Noninvasive urine-derived cell lines derived from neurological genetic patients.

Zhang QJ, He J, Ni W, Lin X, Yao XP, Lin MT, Murong SX, Wang N, Chen WJ. Zhang QJ, et al. Among authors: wang n. Neuroreport. 2013 Mar 6;24(4):161-6. doi: 10.1097/WNR.0b013e32835e2e44. Neuroreport. 2013. PMID: 23358449

8

PRRT2 mutation correlated with phenotype of paroxysmal kinesigenic dyskinesia and drug response.

Li HF, Chen WJ, Ni W, Wang KY, Liu GL, Wang N, Xiong ZQ, Xu J, Wu ZY. Li HF, et al. Among authors: wang ky, wang n. Neurology. 2013 Apr 16;80(16):1534-5. doi: 10.1212/WNL.0b013e31828cf7e1. Epub 2013 Mar 27. Neurology. 2013. PMID: 23535490 No abstract available.

9

Molecular analysis of the dystrophin gene in 407 Chinese patients with Duchenne/Becker muscular dystrophy by the combination of multiplex ligation-dependent probe amplification and Sanger sequencing.

Chen WJ, Lin QF, Zhang QJ, He J, Liu XY, Lin MT, Murong SX, Liou CW, Wang N. Chen WJ, et al. Among authors: wang n. Clin Chim Acta. 2013 Aug 23;423:35-8. doi: 10.1016/j.cca.2013.04.006. Epub 2013 Apr 13. Clin Chim Acta. 2013. PMID: 23588064

10

Association between G2385R and R1628P polymorphism of LRRK2 gene and sporadic Parkinson's disease in a Han-Chinese population in south-eastern China.

Cai J, Lin Y, Chen W, Lin Q, Cai B, Wang N, Zheng W. Cai J, et al. Among authors: wang n. Neurol Sci. 2013 Nov;34(11):2001-6. doi: 10.1007/s10072-013-1436-3. Epub 2013 Apr 30. Neurol Sci. 2013. PMID: 23624603

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