Wu ZY - Search Results

1

Mutation analysis of 218 Chinese patients with Wilson disease revealed no correlation between the canine copper toxicosis gene MURR1 and Wilson disease.

Wu ZY, Zhao GX, Chen WJ, Wang N, Wan B, Lin MT, Murong SX, Yu L. Wu ZY, et al. J Mol Med (Berl). 2006 May;84(5):438-42. doi: 10.1007/s00109-005-0036-y. Epub 2006 Jan 28. J Mol Med (Berl). 2006. PMID: 16649058

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. 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. 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: wu zy. 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. 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. 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: wu zy. 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: wu zy. 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

Quantitative studies on SMN1 gene and carrier testing of spinal muscular atrophy.

Chen WJ, Wu ZY, Wang N, Lin MT, Mu-rong SX. Chen WJ, et al. Among authors: wu zy. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Dec;22(6):559-602. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005. PMID: 16331551

10

[Clinical analysis of dopa-responsive dystonia and mutation analysis of the GCH I gene].

Xie H, Wu ZY, Wang N, Li ZW, Lin MT, Murong SX. Xie H, et al. Among authors: wu zy. Zhonghua Er Ke Za Zhi. 2006 Jul;44(7):492-5. Zhonghua Er Ke Za Zhi. 2006. PMID: 17044972 Chinese.

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