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[Genotype and phenotype of female Dravet syndrome with PCDH19 mutations].
Liu AJ, Zhang YH, Xu XJ, Yang XL, Yang ZX, Wu Y, Liu XY, Jiang YW, Wu XR. Liu AJ, et al. Among authors: jiang yw. Zhonghua Er Ke Za Zhi. 2016 May;54(5):327-31. doi: 10.3760/cma.j.issn.0578-1310.2016.05.004. Zhonghua Er Ke Za Zhi. 2016. PMID: 27143072 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: jiang yw. 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 analysis of neuromyelitis optica spectrum disorders in childhood].
Zhou J, Zhang Y, Ji TY, Jin YW, Bao XH, Zhang YH, Xiong H, Chang XZ, Jiang YW, Wu Y. Zhou J, et al. Among authors: jiang yw. Zhonghua Er Ke Za Zhi. 2019 Feb 2;57(2):118-124. doi: 10.3760/cma.j.issn.0578-1310.2019.02.011. Zhonghua Er Ke Za Zhi. 2019. PMID: 30695886 Chinese.
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