Yang X - Search Results

1

The Genetic Landscape of Epilepsy of Infancy with Migrating Focal Seizures.

Burgess R, Wang S, McTague A, Boysen KE, Yang X, Zeng Q, Myers KA, Rochtus A, Trivisano M, Gill D; EIMFS Consortium; Sadleir LG, Specchio N, Guerrini R, Marini C, Zhang YH, Mefford HC, Kurian MA, Poduri AH, Scheffer IE. Burgess R, et al. Among authors: yang x. Ann Neurol. 2019 Dec;86(6):821-831. doi: 10.1002/ana.25619. Ann Neurol. 2019. PMID: 31618474 Free PMC 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: yang z. BMC Neurol. 2013 Dec 26;13:209. doi: 10.1186/1471-2377-13-209. BMC Neurol. 2013. PMID: 24370076 Free PMC article.

3

Clinical diagnosis, treatment, and ALDH7A1 mutations in pyridoxine-dependent epilepsy in three Chinese infants.

Yang Z, Yang X, Wu Y, Wang J, Zhang Y, Xiong H, Jiang Y, Qin J. Yang Z, et al. Among authors: yang x. PLoS One. 2014 Mar 24;9(3):e92803. doi: 10.1371/journal.pone.0092803. eCollection 2014. PLoS One. 2014. PMID: 24664145 Free PMC article. Clinical Trial.

4

ATP1A3 mutations and genotype-phenotype correlation of alternating hemiplegia of childhood in Chinese patients.

Yang X, Gao H, Zhang J, Xu X, Liu X, Wu X, Wei L, Zhang Y. Yang X, et al. PLoS One. 2014 May 19;9(5):e97274. doi: 10.1371/journal.pone.0097274. eCollection 2014. PLoS One. 2014. PMID: 24842602 Free PMC article.

5

[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: yang z. 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.

6

[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: yang z. Zhonghua Er Ke Za Zhi. 2014 Nov;52(11):806-11. Zhonghua Er Ke Za Zhi. 2014. PMID: 25582463 Chinese.

7

[ATP1A3 gene mutations in patients with alternating hemiplegia of childhood].

Yang X, Zhang Y, Yuan D, Xu X, Li S, Wei L, Wu Y, Xiong H, Liu X, Bao X, Jiang Y, Wu X. Yang X, et al. Zhonghua Er Ke Za Zhi. 2015 Nov;53(11):835-9. Zhonghua Er Ke Za Zhi. 2015. PMID: 26758322 Chinese.

8

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: yang z. 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

9

Genomic mosaicism in paternal sperm and multiple parental tissues in a Dravet syndrome cohort.

Yang X, Liu A, Xu X, Yang X, Zeng Q, Ye AY, Yu Z, Wang S, Huang AY, Wu X, Wu Q, Wei L, Zhang Y. Yang X, et al. Sci Rep. 2017 Nov 15;7(1):15677. doi: 10.1038/s41598-017-15814-7. Sci Rep. 2017. PMID: 29142202 Free PMC article.

10

Severe infantile onset developmental and epileptic encephalopathy caused by mutations in autophagy gene WDR45.

Carvill GL, Liu A, Mandelstam S, Schneider A, Lacroix A, Zemel M, McMahon JM, Bello-Espinosa L, Mackay M, Wallace G, Waak M, Zhang J, Yang X, Malone S, Zhang YH, Mefford HC, Scheffer IE. Carvill GL, et al. Among authors: yang x. Epilepsia. 2018 Jan;59(1):e5-e13. doi: 10.1111/epi.13957. Epub 2017 Nov 24. Epilepsia. 2018. PMID: 29171013 Free PMC article.

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