A de novo heterozygous variant in ACOX1 gene cause Mitchell syndrome: the first case in China and literature review von Shen, Mengxiao, Chen, Qian, Gao, Yanyan, Yan, Hongyu, Feng, Shuo, Ji, Xinna, Zhang, Xue

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Generation of a human iPSC line CIPi004-A from a patient with neurofibromatosis type 1 and epilepsy harboring a heterozygous mutation in NF1 gene von Wu, Fan, Ji, Xinna, Gao, Yanyan, Liu, Wanting, Lu, Yuanfang, Yang, Aiyun, Wang, Jianhua, Chen, Qian, Zhang, Xue

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Generation of a human induced pluripotent stem cell line (CIPi002-A) from an early infantile epileptic encephalopathy patient with a heterozygous mutation in SCN8A von Zhang, Pingping, Zheng, Ping, Ji, Xinna, Gao, Yanyan, Zhang, Xue, Chen, Qian

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Generation of a human iPSC line CIPi003-A from a patient with focal epilepsy harboring a heterozygous mutation in DEPDC5 gene von Shen, Mengxiao, Fan, Shiqi, Wu, Fan, Cheng, Peidi, Gao, Yanyan, Zheng, Ping, Feng, Shuo, Ji, Xinna, Chen, Qian, Zhang, Xue

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Pediatric Autoimmune Encephalitis: Case Series From Two Chinese Tertiary Pediatric Neurology Centers von Zhang, Jianzhao, Ji, Taoyun, Chen, Qian, Jiang, Yanan, Cheng, Huan, Zheng, Ping, Ma, Wenqiang, Lei, Ting, Zhang, Yao, Jin, Yiwen, Wei, Cuijie, Wu, Ye, Chang, Xingzhi, Bao, Xinhua, Zhang, Yuehua, Xiong, Hui, Ji, Xinna, Feng, Shuo, Ren, Haitao, Yang, Jian, Jiang, Yuwu

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Generation of a human iPSC line CIPi001-A from a benign familial infantile epilepsy patient related 16p11.2 deletion von Ji, Xinna, Gao, Yanyan, Zhang, Pingping, Jin, Ziqi, Zhang, Yan, Yang, Minna, Zhang, Xue, Chen, Qian

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Whole exome sequencing identifies KCNH7 variants associated with epilepsy in children von Wu, Fan, Ji, Xinna, Shen, Mengxiao, Cheng, Peidi, Feng, Shuo, Gao, Yanyan, Liu, Wanting, Chen, Jinxiao, Li, Shupin, Zhang, Xue, Chen, Qian

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Nitric oxide-mediated neuronal apoptosis in rats with recurrent febrile seizures through endoplasmic reticulum stress pathway von Chen, Jing, Qin, Jiong, Liu, Xiaoyan, Han, Ying, Yang, Zhixian, Chang, Xingzhi, Ji, Xinna

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Prevalence, clinical characteristics and outcomes of seizures in neurofibromatosis type 1: A systematic review and single arm meta-analysis von Wu, Fan, Ji, Xinna, Shen, Mengxiao, Cheng, Peidi, Gao, Yanyan, Liu, Wanting, Chen, Jinxiao, Feng, Shuo, Wu, Huanhuan, Di, Fei, Li, Yunlin, Wang, Jianhua, Zhang, Xue, Chen, Qian

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不明原因智力障碍或发育迟缓患儿已知基因的新生点变异研究 von 高志杰, 姜茜, 陈晓丽, 陈倩, 姬辛娜, 毛莹莹, 冯硕, 董静静, 许克铭

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Generalized Lottery Trees: Budget-Consistent Incentive Tree Mechanisms for Crowdsourcing von Zhao, Dong, Ma, Huadong, Ji, Xinna

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Generalized Lottery Trees: Budget-Consistent Incentive Tree Mechanisms for Crowdsourcing von Zhao, Dong, Ma, Huadong, Ji, Xinna

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Generalized Lottery Trees: Budget-Balanced Incentive Tree Mechanisms for Crowdsourcing von Zhao, Dong, Ma, Huadong, Ji, Xinna

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Portable electroencephalogram and myoelectricity equipment with AI intelligent analysis function von FENG SHUO, CHEN QIAN, JI XINNA, GAO YANYAN, CHEN JINXIAO

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Assertion program processing method and device, equipment, medium and product von MA GUOJUN, JI XINNA, WU HAO, FEI ZHIHUI

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Myasthenia examination device von FANG PING, CHEN QIAN, YANG YING, ZHAO JIAWEI, JI XINNA

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Detection card suitable for portable spectrophotometer von XIE LINA, FENG SHUO, CHEN QIAN, GOU MO, GAO YANYAN, JI XINNA, MAO YINGYING, ZHANG PINGPING, WEI XING

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Combined methylmalonic acidemia gene mutation detection kit von XIE LINA, FENG SHUO, CHEN QIAN, XIAO JIANGSHAN, GAO YANYAN, JI XINNA, YU CHAOJI, ZHENG PING, MAO YINGYING, ZHANG PINGPING, WEI XING

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POCT detection method for content of hypoxanthine in urine and application von XIE LINA, FENG SHUO, CHEN QIAN, XIAO JIANGSHAN, GAO YANYAN, JI XINNA, YU CHAOJI, MAO YINGYING, ZHANG PINGPING, WEI XING

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Target search system and method von LIU LIANG, YANG HAO, MA HUADONG, JI XINNA, ZHAO DONG

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