Sun HH - Search Results

1

[Genetic and phenotypic characteristics of SCN1A mutations in Dravet syndrome].

Xu XJ, Zhang YH, Sun HH, Liu XY, Jiang YW, Wu XR. Xu XJ, et al. Among authors: sun hh. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012 Dec;29(6):625-30. doi: 10.3760/cma.j.issn.1003-9406.2012.06.001. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012. PMID: 23225037 Chinese.

2

[Progress in molecular genetics of generalized epilepsy with febrile seizures plus].

Sun HH, Zhang YH. Sun HH, et al. Beijing Da Xue Xue Bao Yi Xue Ban. 2008 Apr;40(2):229-33. Beijing Da Xue Xue Bao Yi Xue Ban. 2008. PMID: 18458705 Free article. Review. Chinese.

3

Seven novel SCN1A mutations in Chinese patients with severe myoclonic epilepsy of infancy.

Sun H, Zhang Y, Liang J, Liu X, Ma X, Qin J, Qi Y, Wu X. Sun H, et al. Epilepsia. 2008 Jun;49(6):1104-7. doi: 10.1111/j.1528-1167.2008.01549_2.x. Epilepsia. 2008. PMID: 18554359 Free article. No abstract available.

4

SCN1A, SCN1B, and GABRG2 gene mutation analysis in Chinese families with generalized epilepsy with febrile seizures plus.

Sun H, Zhang Y, Liang J, Liu X, Ma X, Wu H, Xu K, Qin J, Qi Y, Wu X. Sun H, et al. J Hum Genet. 2008;53(8):769-774. doi: 10.1007/s10038-008-0306-y. Epub 2008 Jun 20. J Hum Genet. 2008. PMID: 18566737

5

Gene symbol: SCN1A. Disease: Generalized epilepsy with febrile seizures plus.

Sun H, Zhang Y, Liang J, Liu X, Ma X, Wu H, Xu K, Qin J, Qi Y, Wu X. Sun H, et al. Hum Genet. 2008 Oct;124(3):298. Hum Genet. 2008. PMID: 18846618 No abstract available.

6

Gene symbol: GABRG2. Disease: Generalized epilepsy with febrile seizures plus.

Sun H, Zhang Y, Liang J, Liu X, Ma X, Wu H, Xu K, Qin J, Qi Y, Wu X. Sun H, et al. Hum Genet. 2008 Oct;124(3):298. Hum Genet. 2008. PMID: 18846619 No abstract available.

7

[Analysis of the GABRG2 gene mutation in a Chinese family with generalized epilepsy with febrile seizures plus].

Sun H, Zhang Y, Liu X, Ma X, Wu H, Xu K, Qi Y, Wu X. Sun H, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008 Dec;25(6):611-5. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008. PMID: 19065515 Chinese.

8

[Progress in molecular genetics in severe myoclonic epilepsy of infancy].

Sun HH, Zhang YH. Sun HH, et al. Zhonghua Er Ke Za Zhi. 2008 Feb;46(2):157-60. Zhonghua Er Ke Za Zhi. 2008. PMID: 19099699 Review. Chinese. No abstract available.

9

[Clinical features and SCN1A gene mutation analysis of severe myoclonic epilepsy of infancy].

Zhang YH, Sun HH, Liu XY, Ma XW, Yang ZX, Xiong H, Qin J, Lin Q, Wu XR. Zhang YH, et al. Among authors: sun hh. Zhonghua Er Ke Za Zhi. 2008 Oct;46(10):769-73. Zhonghua Er Ke Za Zhi. 2008. PMID: 19099883 Chinese.

10

[Mutation analysis of the SCN1A gene in severe myoclonic epilepsy of infancy].

Sun H, Zhang Y, Liu X, Ma X, Wu H, Xu K, Qin J, Qi Y, Wu X. Sun H, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009 Apr;26(2):121-7. doi: 10.3760/cma.j.issn.1003-9406.2009.02.001. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009. PMID: 19350499 Chinese.

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