Intercropping with wheat suppressed Fusarium wilt in faba bean and modulated the composition of root exudates von Lv, Jiaxing, Dong, Yan, Dong, Kun, Zhao, Qian, Yang, Zhixian, Chen, Ling

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Automatic Diagnosis of Epileptic Seizure in Electroencephalography Signals Using Nonlinear Dynamics Features von Chen, Shanen, Zhang, Xi, Chen, Lili, Yang, Zhixian

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The relationship between the characteristics of burst suppression pattern and different etiologies in epilepsy von Yang, Haipo, Gong, Pan, Jiao, Xianru, Zhou, Qiujun, Zhang, Yuehua, Jiang, Yuwu, Yang, Zhixian

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POLR3-related leukodystrophy caused by biallelic POLR3A and 1C pathogenic variants: a single-center experience von Liu, Jing, Niu, Yue, Qin, Jiong, Yang, Zhixian

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A long journey to treat epilepsy with the gut microbiota von Li, Qinrui, Gu, Youyu, Liang, Jingjing, Yang, Zhixian, Qin, Jiong

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Genetic Etiologies in Developmental and/or Epileptic Encephalopathy With Electrical Status Epilepticus During Sleep: Cohort Study von Gong, Pan, Xue, Jiao, Jiao, Xianru, Zhang, Yuehua, Yang, Zhixian

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Case Report: Causative De novo Variants of KCNT2 for Developmental and Epileptic Encephalopathy von Gong, Pan, Jiao, Xianru, Yu, Dan, Yang, Zhixian

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Variants loci and phenotype correlation of TRIM8- related neuro-renal syndrome: three cases reports and literature review von Lv, Qiu, Niu, Yue, Xu, Zhao, Qin, Jiong, Yang, Zhixian

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Long-term outcomes of epilepsy surgery in tuberous sclerosis complex von Liang, Shuli, Zhang, Juncheng, Yang, Zhixian, Zhang, Shaohui, Cui, Zhiqiang, Cui, Jianfei, Zhang, Jiwu, Liu, Na, Ding, Ping

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CHD2‐related epilepsy: novel mutations and new phenotypes von Chen, Jiaoyang, Zhang, Jing, Liu, Aijie, Zhang, Liping, Li, Hua, Zeng, Qi, Yang, Zhixian, Yang, Xiaoling, Wu, Xiru, Zhang, Yuehua

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Generation of a human iPSC line from an epileptic encephalopathy patient with electrical status epilepticus during sleep carrying KCNA2 (p.P405L) mutation von Gong, Pan, Jiao, Xianru, Zhang, Yuehua, Yang, Zhixian

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The clinical outcome and neuroimaging of acute encephalopathy after status epilepticus in Dravet syndrome von Tian, Xiaojuan, Ye, Jintang, Zeng, Qi, Zhang, Jing, Yang, Xiaoling, Liu, Aijie, Yang, Zhixian, Liu, Xiaoyan, Wu, Xiru, Zhang, Yuehua

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Case Report: A Case of Epileptic Disorder Associated With a Novel CNTN2 Frameshift Variant in Homozygosity due to Maternal Uniparental Disomy von Chen, Wenjie, Chen, Fei, Shen, Yiping, Yang, Zhixian, Qin, Jiong

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Clinical and genetic analysis of two Chinese infants with Mabry syndrome von Xue, Jiao, Li, Hui, Zhang, Yuehua, Yang, Zhixian

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A Feature Extraction Method for P2P Botnet Detection Using Graphic Symmetry Concept von Yang, Zhixian, Wang, Buhong

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GABRB3-related epilepsy: novel variants, clinical features and therapeutic implications von Yang, Ying, Zeng, Qi, Cheng, Miaomiao, Niu, Xueyang, Xiangwei, Wenshu, Gong, Pan, Li, Wenhui, Ma, Jiehui, Zhang, Xiaoli, Yang, Xiaoling, Yang, Zhixian, Sun, Dan, Zhou, Shuizhen, Liao, Jianxiang, Jiang, Yuwu, Zhang, Yuehua

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A Rare Presentation Characterized by Epileptic Spasms in ALDH7A1 , Pyridox(am)ine-5'-Phosphate Oxidase, and PLPBP Deficiency von Jiao, Xianru, Gong, Pan, Niu, Yue, Zhang, Yuehua, Yang, Zhixian

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Complex Mosaicism of Two Distinct Mutations in a Female Patient With KCNA2-Related Encephalopathy: A Case Report von Gong, Pan, Jiao, Xianru, Zhang, Yuehua, Yang, Zhixian

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Analyzing clinical and genetic characteristics of a cohort with multiple congenital anomalies-hypotonia-seizures syndrome (MCAHS) von Jiao, Xianru, Xue, Jiao, Gong, Pan, Bao, Xinhua, Wu, Ye, Zhang, Yuehua, Jiang, Yuwu, Yang, Zhixian

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GRIN2A mutations in epilepsy-aphasia spectrum disorders von Yang, Xiaoling, Qian, Ping, Xu, Xiaojing, Liu, Xiaoyan, Wu, Xiru, Zhang, Yuehua, Yang, Zhixian

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