Wu X - Search Results

1

Infantile epilepsy with multifocal myoclonus caused by TBC1D24 mutations.

Zhang J, Chen J, Zeng Q, Zhang L, Tian X, Yang X, Yang Z, Wu Y, Wu X, Zhang Y. Zhang J, et al. Among authors: wu y, wu x. Seizure. 2019 Jul;69:228-234. doi: 10.1016/j.seizure.2019.05.010. Epub 2019 May 13. Seizure. 2019. PMID: 31112829 Free article.

2

Phenotypes and PRRT2 mutations in Chinese families with benign familial infantile epilepsy and infantile convulsions with paroxysmal choreoathetosis.

Yang X, Zhang Y, Xu X, Wang S, Yang Z, Wu Y, Liu X, Wu X. Yang X, et al. Among authors: wu y, wu x. BMC Neurol. 2013 Dec 26;13:209. doi: 10.1186/1471-2377-13-209. BMC Neurol. 2013. PMID: 24370076 Free PMC article.

3

[Phenotypes and PRRT2 mutation analysis in families with benign familial infantile epilepsy].

Yang X, Zhang Y, Xu X, Yu X, Zhang X, Yang Z, Wang S, Wu Y, Liu X, Wu X. Yang X, et al. Among authors: wu y, wu x. Zhonghua Er Ke Za Zhi. 2014 Nov;52(11):806-11. Zhonghua Er Ke Za Zhi. 2014. PMID: 25582463 Chinese.

4

CHD2-related epilepsy: novel mutations and new phenotypes.

Chen J, Zhang J, Liu A, Zhang L, Li H, Zeng Q, Yang Z, Yang X, Wu X, Zhang Y. Chen J, et al. Among authors: wu x. Dev Med Child Neurol. 2020 May;62(5):647-653. doi: 10.1111/dmcn.14367. Epub 2019 Nov 1. Dev Med Child Neurol. 2020. PMID: 31677157 Free article.

5

[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.

6

Epilepsy in children with methylmalonic acidemia: electroclinical features and prognosis.

Ma X, Zhang Y, Yang Y, Liu X, Yang Z, Bao X, Qin J, Wu X. Ma X, et al. Among authors: wu x. Brain Dev. 2011 Oct;33(9):790-5. doi: 10.1016/j.braindev.2011.06.001. Epub 2011 Jul 20. Brain Dev. 2011. PMID: 21764232

7

Early clinical features and diagnosis of Dravet syndrome in 138 Chinese patients with SCN1A mutations.

Xu X, Zhang Y, Sun H, Liu X, Yang X, Xiong H, Jiang Y, Bao X, Wang S, Yang Z, Wu Y, Qin J, Lin Q, Wu X. Xu X, et al. Among authors: wu y, wu x. Brain Dev. 2014 Sep;36(8):676-81. doi: 10.1016/j.braindev.2013.10.004. Epub 2013 Oct 26. Brain Dev. 2014. PMID: 24168886

8

[Clinical features and PRRT2 mutations in infantile convulsions with paroxysmal choreoathetosis].

Yang X, Zhang Y, Xu X, Wang S, Yang Z, Wu Y, Zhang X, Liu X, Wu X. Yang X, et al. Among authors: wu y, wu x. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014 Dec;31(6):679-85. doi: 10.3760/cma.j.issn.1003-9406.2014.06.001. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014. PMID: 25449067 Chinese.

9

GRIN2A mutations in epilepsy-aphasia spectrum disorders.

Yang X, Qian P, Xu X, Liu X, Wu X, Zhang Y, Yang Z. Yang X, et al. Among authors: wu x. Brain Dev. 2018 Mar;40(3):205-210. doi: 10.1016/j.braindev.2017.09.007. Epub 2017 Oct 19. Brain Dev. 2018. PMID: 29056244

10

[Analysis of SCN1A deletions or duplications in patients with Dravet syndrome].

Zeng Q, Zhang Y, Yang X, Xu X, Zhang J, Tian X, Liu A, Liu X, Jiang Y, Wu X. Zeng Q, et al. Among authors: wu x. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Dec 10;34(6):787-791. doi: 10.3760/cma.j.issn.1003-9406.2017.06.001. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 29188601 Chinese.

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