Zhang YH - 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: zhang yh. Ann Neurol. 2019 Dec;86(6):821-831. doi: 10.1002/ana.25619. Ann Neurol. 2019. PMID: 31618474 Free PMC article.

2

Association between genetic variation of CACNA1H and childhood absence epilepsy.

Chen Y, Lu J, Pan H, Zhang Y, Wu H, Xu K, Liu X, Jiang Y, Bao X, Yao Z, Ding K, Lo WH, Qiang B, Chan P, Shen Y, Wu X. Chen Y, et al. Ann Neurol. 2003 Aug;54(2):239-43. doi: 10.1002/ana.10607. Ann Neurol. 2003. PMID: 12891677

3

[Research on genes susceptible to childhood absence epilepsy].

Liang JM, Zhang YH, Wu XR. Liang JM, et al. Among authors: zhang yh. 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.

4

Dravet syndrome or genetic (generalized) epilepsy with febrile seizures plus?

Scheffer IE, Zhang YH, Jansen FE, Dibbens L. Scheffer IE, et al. Among authors: zhang yh. Brain Dev. 2009 May;31(5):394-400. doi: 10.1016/j.braindev.2009.01.001. Epub 2009 Feb 8. Brain Dev. 2009. PMID: 19203856 Review.

5

Genetics of the epilepsies: genetic twists in the channels and other tales.

Scheffer IE, Zhang YH, Gecz J, Dibbens L. Scheffer IE, et al. Among authors: zhang yh. Epilepsia. 2010 Feb;51 Suppl 1:33-6. doi: 10.1111/j.1528-1167.2009.02440.x. Epilepsia. 2010. PMID: 20331710 Free article. No abstract available.

6

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. 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

7

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. BMC Neurol. 2013 Dec 26;13:209. doi: 10.1186/1471-2377-13-209. BMC Neurol. 2013. PMID: 24370076 Free PMC article.

8

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. 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.

9

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.

10

[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. 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.

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