Efficacy and safety of Bacteroides fragilis BF839 for pediatric autism spectrum disorder: a randomized clinical trial by Chu-hui Lin, Ting Zeng, Cui-wei Lu, De-yang Li, De-yang Li, Yi-ying Liu, Bing-mei Li, Bing-mei Li, Sheng-qiang Chen, Yu-hong Deng, Yu-hong Deng, Yu-hong Deng

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SHROOM4 Variants Are Associated With X-Linked Epilepsy With Features of Generalized Seizures or Generalized Discharges by Wen-Jun Bian, Zong-Jun Li, Jie Wang, Sheng Luo, Bing-Mei Li, Liang-Di Gao, Na He, Yong-Hong Yi

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De novo GABRA1 variants in childhood epilepsies and the molecular subregional effects by Wen-Hui Liu, Sheng Luo, Dong-Ming Zhang, Zi-Sheng Lin, Song Lan, Xin Li, Yi-Wu Shi, Tao Su, Yong-Hong Yi, Peng Zhou, Bing-Mei Li

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PRRT2 gene mutations associated with infantile convulsions induced by sucking and the genotype-phenotype correlation by De-Tian Liu, Xue-Qing Tang, Rui-Ping Wan, Sheng Luo, Bao-Zhu Guan, Bin Li, Li-Hong Liu, Bing-Mei Li, Zhi-Gang Liu, Long-Shan Xie, Yong-Hong Yi

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RYR2 Mutations Are Associated With Benign Epilepsy of Childhood With Centrotemporal Spikes With or Without Arrhythmia by Mei-Gang Ma, Mei-Gang Ma, Xiao-Rong Liu, Yuan Wu, Jie Wang, Bing-Mei Li, Yi-Wu Shi, Tao Su, Bin Li, De-Tian Liu, Yong-Hong Yi, Wei-Ping Liao

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Heterozygous PGM3 Variants Are Associated With Idiopathic Focal Epilepsy With Incomplete Penetrance by Xiao-Rong Liu, Wen-Jun Bian, Jie Wang, Ting-Ting Ye, Bing-Mei Li, De-Tian Liu, Bin Tang, Wei-Wen Deng, Yi-Wu Shi, Tao Su, Yong-Hong Yi, Wei-Ping Liao

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GRIN2A Variants Associated With Idiopathic Generalized Epilepsies by Xiao-Rong Liu, Xing-Xing Xu, Si-Mei Lin, Cui-Ying Fan, Ting-Ting Ye, Bin Tang, Yi-Wu Shi, Tao Su, Bing-Mei Li, Yong-Hong Yi, Jian-Hong Luo, Wei-Ping Liao

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SZT2 variants associated with partial epilepsy or epileptic encephalopathy and the genotype-phenotype correlation by Sheng Luo, Xing-Guang Ye, Liang Jin, Liang Jin, Huan Li, Yun-Yan He, Bao-Zhu Guan, Liang-Di Gao, Xiao-Yu Liang, Peng-Yu Wang, Xin-Guo Lu, Hong-Jun Yan, Bing-Mei Li, Yong-Jun Chen, Zhi-Gang Liu, Zhi-Gang Liu

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CACNA1A Mutations Associated With Epilepsies and Their Molecular Sub-Regional Implications by Xue-Lian Li, Xue-Lian Li, Zong-Jun Li, Xiao-Yu Liang, De-Tian Liu, Mi Jiang, Liang-Di Gao, Huan Li, Xue-Qing Tang, Yi-Wu Shi, Bing-Mei Li, Na He, Bin Li, Wen-Jun Bian, Yong-Hong Yi, Chuan-Fang Cheng, Chuan-Fang Cheng, Jie Wang

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Recessive LAMA5 Variants Associated With Partial Epilepsy and Spasms in Infancy by Sheng Luo, Zhi-Gang Liu, Zhi-Gang Liu, Juan Wang, Jun-Xia Luo, Xing-Guang Ye, Xing-Guang Ye, Xin Li, Qiong-Xiang Zhai, Xiao-Rong Liu, Jie Wang, Liang-Di Gao, Fu-Li Liu, Zi-Long Ye, Huan Li, Zai-Fen Gao, Qing-Hui Guo, Bing-Mei Li, Yong-Hong Yi, Wei-Ping Liao

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HCFC1 variants in the proteolysis domain are associated with X‐linked idiopathic partial epilepsy: Exploring the underlying mechanism by Na He, Bao‐Zhu Guan, Jie Wang, Han‐Kui Liu, Yong Mao, Zhi‐Gang Liu, Fei Yin, Jing Peng, Bo Xiao, Bei‐sha Tang, Dong Zhou, Guang Huang, Qi‐Lin Dai, Ying Zeng, Hong Han, Qiong‐Xiang Zhai, Bin Li, Bin Tang, Wen‐Bin Li, Wang Song, Liu Liu, Yi‐Wu Shi, Bing‐Mei Li, Tao Su, Peng Zhou, Xiao‐Rong Liu, Li‐Wu Guo, Yong‐Hong Yi, Wei‐Ping Liao

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