Sun H - Search Results

1

[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.

2

[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.

3

[Phenotype and SCN1A gene mutation screening in 39 families with generalized epilepsy with febrile seizures plus].

Xu XJ, Zhang YH, Sun HH, Liu XY, Wu HS, Wu XR. Xu XJ, et al. Zhonghua Er Ke Za Zhi. 2012 Aug;50(8):580-6. Zhonghua Er Ke Za Zhi. 2012. PMID: 23158734 Chinese.

4

[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. 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.

5

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

6

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.

7

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.

8

[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.

9

Analysis of SCN1A mutation and parental origin in patients with Dravet syndrome.

Sun H, Zhang Y, Liu X, Ma X, Yang Z, Qin J, Jiang Y, Qi Y, Wu X. Sun H, et al. J Hum Genet. 2010 Jul;55(7):421-7. doi: 10.1038/jhg.2010.39. Epub 2010 Apr 30. J Hum Genet. 2010. PMID: 20431604

10

[Analysis of parental origin of de novo SCN1A mutations in Dravet syndrome].

Sun H, Zhang Y, Xu X, Liu X, Wu X. Sun H, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015 Aug;32(4):457-61. doi: 10.3760/cma.j.issn.1003-9406.2015.04.001. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015. PMID: 26252084 Chinese.

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