Huang YN - 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. Among authors: huang yn. Zhonghua Yi Xue Za Zhi. 2004 Jul 17;84(14):1175-80. Zhonghua Yi Xue Za Zhi. 2004. PMID: 15387979 Chinese.

2

[Hyperhomocysteine, methylenetetrahydrofolate reductase gene, and other risk factors in ischemic stroke].

Huang Y, Zhao Yl Yl, Li S. Huang Y, et al. Zhonghua Yi Xue Za Zhi. 2002 Jan 25;82(2):119-22. Zhonghua Yi Xue Za Zhi. 2002. PMID: 11953142 Chinese.

3

[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: huang yn. 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.

4

[The cerebral function monitoring in severe cerebral vascular disease].

Guo ZH, He JT, Jia ZR, Shi X, Wang WW, Huang YN. Guo ZH, et al. Among authors: huang yn. Zhonghua Yi Xue Za Zhi. 2006 Aug 22;86(31):2192-6. Zhonghua Yi Xue Za Zhi. 2006. PMID: 17064505 Chinese.

5

[Significance of sympathetic skin response in diagnosis diabetic small fiber neuropathy].

Wang HX, Jia ZR, Shi X, Liang W, Sun XR, Huang YN. Wang HX, et al. Among authors: huang yn. Zhonghua Yi Xue Za Zhi. 2008 Jul 1;88(25):1753-5. Zhonghua Yi Xue Za Zhi. 2008. PMID: 19035085 Chinese.

6

[Tumor-like inflammatory demyelinating diseases of the central nervous system with relapse onset: a case report and review].

Qi XL, Chen J, Zheng RL, Li Y, Huang YN, Yuan Y. Qi XL, et al. Among authors: huang yn. Beijing Da Xue Xue Bao Yi Xue Ban. 2009 Oct 18;41(5):588-9. Beijing Da Xue Xue Bao Yi Xue Ban. 2009. PMID: 19829680 Free article. Chinese.

7

[Mutation analysis of GCDH gene in eight patients with glutaric aciduria type I].

Chen J, Wang ZX, Zhang JL, Yang YL, Chen J, Huang YN. Chen J, et al. Among authors: huang yn. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011 Aug;28(4):374-8. doi: 10.3760/cma.j.issn.1003-9406.2011.04.003. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011. PMID: 21811973 Chinese.

8

Mutations in mitochondrially encoded complex I enzyme as the second common cause in a cohort of Chinese patients with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes.

Zhao D, Hong D, Zhang W, Yao S, Qi X, Lv H, Zheng R, Feng L, Huang Y, Yuan Y, Wang Z. Zhao D, et al. J Hum Genet. 2011 Nov;56(11):759-64. doi: 10.1038/jhg.2011.96. Epub 2011 Aug 18. J Hum Genet. 2011. PMID: 21850008

9

[Investigation of multiple organ involvement in Fabry disease].

Zhang W, Kang M, Zhao Y, Li F, Shu J, Zuo Y, Liu J, Huang Y, Yuan Y. Zhang W, et al. Zhonghua Yi Xue Za Zhi. 2015 Jun 16;95(23):1829-32. Zhonghua Yi Xue Za Zhi. 2015. PMID: 26712400 Chinese.

10

Association of hepatitis E virus infection and myasthenia gravis: A pilot study.

Wang L, Gao F, Lin G, Yuan Y, Huang Y, Hao H, Zhuang H, Wang L. Wang L, et al. J Hepatol. 2018 Jun;68(6):1318-1320. doi: 10.1016/j.jhep.2018.01.040. Epub 2018 Apr 19. J Hepatol. 2018. PMID: 29681394 No abstract available.

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