Zhang YH - Search Results

1

Genetic epilepsy with febrile seizures plus: Refining the spectrum.

Zhang YH, Burgess R, Malone JP, Glubb GC, Helbig KL, Vadlamudi L, Kivity S, Afawi Z, Bleasel A, Grattan-Smith P, Grinton BE, Bellows ST, Vears DF, Damiano JA, Goldberg-Stern H, Korczyn AD, Dibbens LM, Ruzzo EK, Hildebrand MS, Berkovic SF, Scheffer IE. Zhang YH, et al. Neurology. 2017 Sep 19;89(12):1210-1219. doi: 10.1212/WNL.0000000000004384. Epub 2017 Aug 25. Neurology. 2017. PMID: 28842445

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

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. Pediatr Neurol. 2006 Sep;35(3):187-90. doi: 10.1016/j.pediatrneurol.2006.03.006. Pediatr Neurol. 2006. PMID: 16939858

4

[Progress in molecular genetics of generalized epilepsy with febrile seizures plus].

Sun HH, Zhang YH. Sun HH, et al. Among authors: zhang yh. Beijing Da Xue Xue Bao Yi Xue Ban. 2008 Apr;40(2):229-33. Beijing Da Xue Xue Bao Yi Xue Ban. 2008. PMID: 18458705 Free article. Review. 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

Partial seizures and atypical absence seizures as a single ictal event in a patient with Lennox-Gastaut syndrome.

Yang Z, Liu X, Qin J, Zhang Y, Bao X, Xiong H. Yang Z, et al. J Child Neurol. 2008 Nov;23(11):1319-23. doi: 10.1177/0883073808318055. J Child Neurol. 2008. PMID: 18984844

7

[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.

8

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.

9

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.

10

[Electroclinical features of myoclonic-atonic epilepsy].

Deng J, Zhang YH, Liu XY, Yang ZX, Xiong H, Wang S, Bao XH, Jiang YW, Qin J, Lin Q, Wu XR. Deng J, et al. Among authors: zhang yh. Zhonghua Er Ke Za Zhi. 2011 Aug;49(8):577-82. Zhonghua Er Ke Za Zhi. 2011. PMID: 22093418 Chinese.

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