Wang ZX - Search Results

1

[NOTCH3 gene mutations in four Chinese families with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy].

Wang ZX, Lu H, Zhang Y, Bu DF, Niu XY, Zhang Z, Huang YN, Yuan Y. Wang ZX, et al. Zhonghua Yi Xue Za Zhi. 2004 Jul 17;84(14):1175-80. Zhonghua Yi Xue Za Zhi. 2004. PMID: 15387979 Chinese.

2

[Clinical features in 4 Chinese families with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)].

Lv H, Yao S, Zhang W, Wang ZX, Huang YN, Niu XY, Zhang Z, Yuan Y. Lv H, et al. Among authors: wang zx. Beijing Da Xue Xue Bao Yi Xue Ban. 2004 Oct;36(5):496-500. Beijing Da Xue Xue Bao Yi Xue Ban. 2004. PMID: 15489930 Free article. Chinese.

3

Novel GLA gene mutations in two Chinese families with classic Fabry disease.

Wang ZX, Zhang Y, Bu DF, Zhang W, Yuan Y. Wang ZX, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Oct;22(5):489-92. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005. PMID: 16215932

4

[Two novel mutations in palmitoyl-protein thioesterase gene in two Chinese babies with infantile neuronal ceroid lipofuscinosis].

Bi HY, Yao S, Bu DF, Wang ZX, Zhang Y, Qin J, Yang YL, Yuan Y. Bi HY, et al. Among authors: wang zx. Zhonghua Er Ke Za Zhi. 2006 Jul;44(7):496-9. Zhonghua Er Ke Za Zhi. 2006. PMID: 17044973 Chinese.

5

[Mitochondrial DNA mutation analysis in 97 Chinese patients with mitochondrial cephalomyopathy].

Wang ZX, Luan XH, Zhang Y, Yang YL, Qi Y, Bu DF, Yuan Y. Wang ZX, et al. Zhonghua Yi Xue Za Zhi. 2008 Dec 16;88(46):3254-6. Zhonghua Yi Xue Za Zhi. 2008. PMID: 19159548 Chinese.

6

[Clinical characteristics and desmin mutations in patients with desminopathy associated cardiomyopathy from 5 Chinese families].

Hong DJ, Zhang W, Jiang TY, Feng L, Wang ZX, Yuan Y. Hong DJ, et al. Among authors: wang zx. Zhonghua Xin Xue Guan Bing Za Zhi. 2010 May;38(5):420-4. Zhonghua Xin Xue Guan Bing Za Zhi. 2010. PMID: 20654101 Chinese.

7

[Clinical heterogeneity associated with mitochondrial DNA A8344G point mutation].

Zhao J, Zhao DH, Zhang W, Lü H, Yuan Y, Qi Y, Wang ZX. Zhao J, et al. Among authors: wang zx. Zhonghua Yi Xue Za Zhi. 2012 Oct 30;92(40):2835-8. Zhonghua Yi Xue Za Zhi. 2012. PMID: 23290212 Chinese.

8

[Clinical features and acid alpha-glucosidase gene mutation in 7 Chinese patients with glycogen storage disease type II].

Liu Q, Zhao J, Wang ZX, Zhang W, Yuan Y. Liu Q, et al. Among authors: wang zx. Zhonghua Yi Xue Za Zhi. 2013 Jul 2;93(25):1981-5. Zhonghua Yi Xue Za Zhi. 2013. PMID: 24169249 Chinese.

9

[Mitochondrial DNA mutations in patients with chronic progressive external ophthalmoplegia and Kearns-Sayre syndrome].

Wang ZX, Yuan Y, Gao F, Qi Y, Shen DG, Chen QT. Wang ZX, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2003 Aug;20(4):273-8. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2003. PMID: 12903032 Chinese.

10

[Expressions of PDCD5 and other apoptosis-related proteins in muscle of patients with mitochondrial cytopathy].

Li YF, Wang ZX, Gao XG, Hong DJ, Yuan Y. Li YF, et al. Among authors: wang zx. Zhonghua Yi Xue Za Zhi. 2009 Jun 16;89(23):1593-6. Zhonghua Yi Xue Za Zhi. 2009. PMID: 19957502 Chinese.

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