Zhang Y - Search Results

1

Clinical and genetic analysis of two Chinese infants with Mabry syndrome.

Xue J, Li H, Zhang Y, Yang Z. Xue J, et al. Among authors: zhang y. Brain Dev. 2016 Oct;38(9):807-18. doi: 10.1016/j.braindev.2016.04.008. Epub 2016 May 10. Brain Dev. 2016. PMID: 27177984

2

Alpers syndrome with prominent white matter changes.

Bao X, Wu Y, Wong LJ, Zhang Y, Xiong H, Chou PC, Truong CK, Jiang Y, Qin J, Yuan Y, Lin Q, Wu X. Bao X, et al. Among authors: zhang y. Brain Dev. 2008 Apr;30(4):295-300. doi: 10.1016/j.braindev.2007.08.009. Epub 2007 Oct 17. Brain Dev. 2008. PMID: 17923349

3

A study on epileptic negative myoclonus in atypical benign partial epilepsy of childhood.

Yang Z, Liu X, Qin J, Zhang Y, Bao X, Chang X, Wang S, Wu Y, Xiong H. Yang Z, et al. Among authors: zhang y. Brain Dev. 2009 Apr;31(4):274-81. doi: 10.1016/j.braindev.2008.04.004. Epub 2008 Jun 17. Brain Dev. 2009. PMID: 18562140

4

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. Among authors: zhang y. J Child Neurol. 2008 Nov;23(11):1319-23. doi: 10.1177/0883073808318055. J Child Neurol. 2008. PMID: 18984844

5

[Clinical features and SCN1A gene mutation analysis of severe myoclonic epilepsy of infancy].

Zhang YH, Sun HH, Liu XY, Ma XW, Yang ZX, Xiong H, Qin J, Lin Q, Wu XR. Zhang YH, et al. Zhonghua Er Ke Za Zhi. 2008 Oct;46(10):769-73. Zhonghua Er Ke Za Zhi. 2008. PMID: 19099883 Chinese.

6

[Clinical and electrophysiologic studies on epileptic negative myoclonus in atypical benign partial epilepsy of childhood].

Yang ZX, Liu XY, Qin J, Zhang YH, Bao XH, Chang XZ, Wu Y, Xiong H. Yang ZX, et al. Among authors: zhang yh. Zhonghua Er Ke Za Zhi. 2008 Dec;46(12):885-90. Zhonghua Er Ke Za Zhi. 2008. PMID: 19134248 Chinese.

7

Clinical and electrophysiological characteristics of startle epilepsy in childhood.

Yang Z, Liu X, Qin J, Zhang Y, Bao X, Wang S, Chang X. Yang Z, et al. Among authors: zhang y. Clin Neurophysiol. 2010 May;121(5):658-64. doi: 10.1016/j.clinph.2009.12.020. Epub 2010 Jan 13. Clin Neurophysiol. 2010. PMID: 20071222

8

[Clinical and electroencephalographic characteristics of epilepsy with myoclonic absences].

Yang ZX, Liu XY, Qin J, Zhang YH, Wu Y, Jiang YW. Yang ZX, et al. Among authors: zhang yh. Zhonghua Er Ke Za Zhi. 2009 Nov;47(11):862-6. Zhonghua Er Ke Za Zhi. 2009. PMID: 20079001 Chinese.

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: zhang y. 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

Analysis of SCN1A mutation and parental origin in patients with Dravet syndrome.

Sun H, Zhang Y, Liu X, Ma X, Yang Z, Qin J, Jiang Y, Qi Y, Wu X. Sun H, et al. Among authors: zhang y. J Hum Genet. 2010 Jul;55(7):421-7. doi: 10.1038/jhg.2010.39. Epub 2010 Apr 30. J Hum Genet. 2010. PMID: 20431604

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