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CORC

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The Clinical and Genetic Features of Co-occurring Epilepsy and Autism Spectrum Disorder in Chinese Children 期刊论文
FRONTIERS IN NEUROLOGY, 2019, 卷号: 10
作者:  Long, Shasha;  Zhou, Hao;  Li, Shuang;  Wang, Tianqi;  Ma, Yu
收藏  |  浏览/下载：30/0  |  提交时间：2019/12/05
Establishment and utility assessment of posterior reversible encephalopathy syndrome early warning scoring scale establishment and utility assessment of PEWS scale. 期刊论文
BMC neurology, 2019, 卷号: Vol.19 No.1, 页码: 30
作者:  Li-Ping Zou;  Li-Ying Liu;  Hui Li;  Yang-Yang Wang;  Ying Liu
收藏  |  浏览/下载：1/0  |  提交时间：2019/12/13
Establishment and utility assessment of posterior reversible encephalopathy syndrome early warning scoring scale establishment and utility assessment of PEWS scale 期刊论文
BMC Neurology, 2019, 卷号: Vol.19 No.1
作者:  Li-Ping Zou;  Li-Ying Liu;  Hui Li;  Yang-Yang Wang;  Ying Liu
收藏  |  浏览/下载：1/0  |  提交时间：2019/12/13
Prospective study of the efficacy of a ketogenic diet in 20 patients with Dravet syndrome 期刊论文
SEIZURE-EUROPEAN JOURNAL OF EPILEPSY, 2018, 卷号: 60
作者:  Ni, Yan;  Wang, Xin-Hua;  Zhang, Lin-Mei;  Chai, Yi-Ming;  Li, Wen-Hui
收藏  |  浏览/下载：7/0  |  提交时间：2019/12/05
Association between HLA alleles and lamotrigine-induced cutaneous adverse drug reactions in Asian populations: A meta-analysis 期刊论文
SEIZURE-EUROPEAN JOURNAL OF EPILEPSY, 2018, 卷号: Vol.60, 页码: 163-171
作者:  Deng, Yilun;  Li, Shaoping;  Zhang, Lin;  Jin, Hou;  Zou, Xiaoyi
收藏  |  浏览/下载：3/0  |  提交时间：2019/02/25
CNKSR2 mutation causes the X-linked epilepsy-aphasia syndrome:A case report and review of literature 期刊论文
World Journal of Clinical Cases, 2018, 卷号: 6, 期号: 12, 页码: 570-576
作者:  Ying Sun;  Yi-Dan Liu;  Zhi-Feng Xu;  Qing-Xia Kong;  Yan-Ling Wang
收藏  |  浏览/下载：9/0  |  提交时间：2019/12/11
G Mutation">Antimyoclonic Effect of Levetiracetam and Clonazepam Combined Treatment on Myoclonic Epilepsy with Ragged-Red Fiber Syndrome with m.8344A > G Mutation 期刊论文
CHINESE MEDICAL JOURNAL, 2018, 卷号: 131, 期号: 20, 页码: 2433-2438
作者:  Su, Li-Jun;  Wang, Yu-Liang;  Han, Tao;  Qiao, Shan;  Zang, Ke-Jun
收藏  |  浏览/下载：6/0  |  提交时间：2019/12/11
Novel FOXG1 mutations in Chinese patients with Rett syndrome or Rett-like mental retardation 期刊论文
BMC MEDICAL GENETICS, 2017
Zhang, Qingping; Wang, Jiaping; Li, Jiarui; Bao, Xinhua; Zhao, Ying; Zhang, Xiaoying; Wei, Liping; Wu, Xiru
收藏  |  浏览/下载：7/0  |  提交时间：2017/12/03
The clinical spectrum of female epilepsy patients with PCDH19 mutations in a Chinese population 期刊论文
CLINICAL GENETICS, 2017
Liu, A.; Xu, X.; Yang, X.; Jiang, Y.; Yang, Z.; Liu, X.; Wu, Y.; Wu, X.; Wei, L.; Zhang, Y.
收藏  |  浏览/下载：8/0  |  提交时间：2017/12/04
The EEG patterns of two childhood patients with Febrile infection-related epilepsy syndrome(FIRES) 会议论文
第七届CAAE国际癫痫论坛
作者:  Guo Yujie;  Chen Yehong;  Hou guangshun;  Luo junxia;  Hu wandong
收藏  |  浏览/下载：7/0  |  提交时间：2019/12/31

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