Wang N - Search Results

1

The role of apolipoprotein E as a risk factor for an earlier age at onset for Machado-Joseph disease is doubtful.

Zhou Q, Ni W, Dong Y, Wang N, Gan SR, Wu ZY. Zhou Q, et al. Among authors: wang n. PLoS One. 2014 Nov 4;9(11):e111356. doi: 10.1371/journal.pone.0111356. eCollection 2014. PLoS One. 2014. PMID: 25369462 Free PMC article.

2

Molecular diagnosis and prophylactic therapy for presymptomatic Chinese patients with Wilson disease.

Wu ZY, Lin MT, Murong SX, Wang N. Wu ZY, et al. Among authors: wang n. Arch Neurol. 2003 May;60(5):737-41. doi: 10.1001/archneur.60.5.737. Arch Neurol. 2003. PMID: 12756138 Clinical Trial.

3

[Genotype-phenotype correlation of patients with wilson disease in Chinese population].

Wu ZY, Wang N, Lin MT, Fang L, Murong SX. Wu ZY, et al. Among authors: wang n. Zhonghua Yi Xue Za Zhi. 2003 Feb 25;83(4):309-11. Zhonghua Yi Xue Za Zhi. 2003. PMID: 12812649 Chinese.

4

[Mechanism of translocation between chromosomes 4q and 10q in facioscapulohumeral muscular dystrophy].

Wang N, Wu ZY, Wang CD, Wang ZQ, Lin MT, Fang L, Murong SX. Wang N, et al. Among authors: wang cd, wang zq. Zhonghua Yi Xue Za Zhi. 2003 Apr 25;83(8):650-3. Zhonghua Yi Xue Za Zhi. 2003. PMID: 12887821 Chinese.

5

FSHD in Chinese population: characteristics of translocation and genotype-phenotype correlation.

Wu ZY, Wang ZQ, Murong SX, Wang N. Wu ZY, et al. Among authors: wang n, wang zq. Neurology. 2004 Aug 10;63(3):581-3. doi: 10.1212/01.wnl.0000133210.93075.81. Neurology. 2004. PMID: 15304602

6

[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.

7

Gene symbol: GTP cyclohydrolase I (GCH-I). Disease: dopa-responsive dystonia.

Hui xie H, Wu ZY, Wang N, Murong SX. Hui xie H, et al. Among authors: wang n. Hum Genet. 2005 Feb;116(3):235. Hum Genet. 2005. PMID: 15818812 No abstract available.

8

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

9

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

10

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.

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