Liang J - Search Results

1

CACNA1I is not associated with childhood absence epilepsy in the Chinese Han population.

Wang J, Zhang Y, Liang J, Pan H, Wu H, Xu K, Liu X, Jiang Y, Shen Y, Wu X. Wang J, et al. Among authors: liang j. Pediatr Neurol. 2006 Sep;35(3):187-90. doi: 10.1016/j.pediatrneurol.2006.03.006. Pediatr Neurol. 2006. PMID: 16939858

2

[Research on genes susceptible to childhood absence epilepsy].

Liang JM, Zhang YH, Wu XR. Liang JM, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2006 Jun;23(3):298-302. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2006. PMID: 16767668 Review. Chinese.

3

[The effect of CACNA1H gene G773D mutation on calcium channel function].

Wang JL, Han CY, Jing YH, Chen YC, Feng N, Lu JJ, Zhang YH, Pan H, Wu HS, Xu KM, Jiang YW, Liang JM, Wang L, Wang XL, Shen Y, Wu XR. Wang JL, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2006 Aug;23(4):369-73. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2006. PMID: 16883519 Chinese.

4

New variants in the CACNA1H gene identified in childhood absence epilepsy.

Liang J, Zhang Y, Wang J, Pan H, Wu H, Xu K, Liu X, Jiang Y, Shen Y, Wu X. Liang J, et al. Neurosci Lett. 2006 Oct 2;406(1-2):27-32. doi: 10.1016/j.neulet.2006.06.073. Epub 2006 Aug 14. Neurosci Lett. 2006. PMID: 16905256

5

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. Among authors: liang j. 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.

6

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. Among authors: liang j. 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

7

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. Among authors: liang j. Hum Genet. 2008 Oct;124(3):298. Hum Genet. 2008. PMID: 18846618 No abstract available.

8

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. Among authors: liang j. Hum Genet. 2008 Oct;124(3):298. Hum Genet. 2008. PMID: 18846619 No abstract available.

9

Childhood absence epilepsy: Elctroclinical features and diagnostic criteria.

Ma X, Zhang Y, Yang Z, Liu X, Sun H, Qin J, Wu X, Liang J. Ma X, et al. Among authors: liang j. Brain Dev. 2011 Feb;33(2):114-9. doi: 10.1016/j.braindev.2010.02.004. Epub 2010 Apr 7. Brain Dev. 2011. PMID: 20378290

10

Vagus nerve stimulation for pediatric patients with intractable epilepsy between 3 and 6 years of age: study protocol for a double-blind, randomized control trial.

Ji T, Yang Z, Liu Q, Liao J, Yin F, Chen Y, Zou L, Li B, Gao Y, Shu X, Huang S, Gao F, Liang J, Lin SF, Peng J, Song S, Wang J, Che C, Sun W, Tian M, Yang L, Hua Y, Hao Y, Cai L, Li L, Jiang Y. Ji T, et al. Among authors: liang j. Trials. 2019 Jan 14;20(1):44. doi: 10.1186/s13063-018-3087-4. Trials. 2019. PMID: 30642370 Free PMC article.

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