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599 results

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[Clinical features of epilepsies associated with GABRB2 variants].
Yang Y, Zhang YH, Chen JY, Zhang J, Yang XL, Chen Y, Yang ZX, Wu XR. Yang Y, et al. Among authors: wu xr. Zhonghua Er Ke Za Zhi. 2019 Jul 2;57(7):532-537. doi: 10.3760/cma.j.issn.0578-1310.2019.07.008. Zhonghua Er Ke Za Zhi. 2019. PMID: 31269553 Chinese.
[Clinical phenotypes of epilepsy associated with GABRA1 gene variants].
Yang Y, Zhang YH, Chen JY, Ma JH, Sun D, Yang XL, Zhang J, Chen Y, Wu XR. Yang Y, et al. Among authors: wu xr. Zhonghua Er Ke Za Zhi. 2020 Feb 2;58(2):118-122. doi: 10.3760/cma.j.issn.0578-1310.2020.02.010. Zhonghua Er Ke Za Zhi. 2020. PMID: 32102148 Chinese.
[Spectrum of mutations in benign familial neonatal-infantile epilepsy].
Zeng Q, Zhang YH, Yang XL, Pu LH, Zhang J, Liu AJ, Yang ZX, Liu XY, Wu XR. Zeng Q, et al. Among authors: wu xr. Zhonghua Er Ke Za Zhi. 2018 Apr 2;56(4):267-273. doi: 10.3760/cma.j.issn.0578-1310.2018.04.006. Zhonghua Er Ke Za Zhi. 2018. PMID: 29614566 Chinese.
[Phenotype study of SCN2A gene related epilepsy].
Zeng Q, Zhang YH, Yang XL, Zhang J, Liu AJ, Liu XY, Jiang YW, Wu XR. Zeng Q, et al. Among authors: wu xr. Zhonghua Er Ke Za Zhi. 2018 Jul 2;56(7):518-523. doi: 10.3760/cma.j.issn.0578-1310.2018.07.009. Zhonghua Er Ke Za Zhi. 2018. PMID: 29996185 Chinese.
[Clinical phenotypes of TBC1D24 gene related epilepsy].
Zhang J, Zhang YH, Chen JY, Zhang LP, Zeng Q, Tian XJ, Yang ZX, Wu Y, Yang XL, Wu XR. Zhang J, et al. Among authors: wu y, wu xr. Zhonghua Er Ke Za Zhi. 2018 Sep 2;56(9):667-673. doi: 10.3760/cma.j.issn.0578-1310.2018.09.007. Zhonghua Er Ke Za Zhi. 2018. PMID: 30180405 Chinese.
[Clinical characteristics of PCDH19-female limited epilepsy].
Chen Y, Yang XL, Liu AJ, Sun D, Yang Y, Zhang J, Chen JY, Yang ZX, Jiang YW, Wu XR, Zhang YH. Chen Y, et al. Among authors: wu xr. Zhonghua Er Ke Za Zhi. 2019 Nov 2;57(11):857-862. doi: 10.3760/cma.j.issn.0578-1310.2019.11.008. Zhonghua Er Ke Za Zhi. 2019. PMID: 31665840 Chinese.
599 results