Zhang YH - Search Results

1

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.

2

[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.

3

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

4

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.

5

[Phenotype and SCN1A gene mutation screening in 39 families with generalized epilepsy with febrile seizures plus].

Xu XJ, Zhang YH, Sun HH, Liu XY, Wu HS, Wu XR. Xu XJ, et al. Among authors: zhang yh. Zhonghua Er Ke Za Zhi. 2012 Aug;50(8):580-6. Zhonghua Er Ke Za Zhi. 2012. PMID: 23158734 Chinese.

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

ILAE classification of the epilepsies: Position paper of the ILAE Commission for Classification and Terminology.

Scheffer IE, Berkovic S, Capovilla G, Connolly MB, French J, Guilhoto L, Hirsch E, Jain S, Mathern GW, Moshé SL, Nordli DR, Perucca E, Tomson T, Wiebe S, Zhang YH, Zuberi SM. Scheffer IE, et al. Among authors: zhang yh. Epilepsia. 2017 Apr;58(4):512-521. doi: 10.1111/epi.13709. Epub 2017 Mar 8. Epilepsia. 2017. PMID: 28276062 Free PMC article.

8

Myoclonic epilepsy in infancy with preceding or concurrent afebrile generalized tonic-clonic seizures in Chinese children.

Yang Z, Li H, Xue J, Qian P, Liu X, Zhang Y. Yang Z, et al. Brain Dev. 2017 Nov;39(10):828-835. doi: 10.1016/j.braindev.2017.06.007. Epub 2017 Jul 13. Brain Dev. 2017. PMID: 28712486

9

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

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: zhang yh, zhang j. 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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