| Issue Date | Title | Author(s) |
| 2019 | The absence of NIPA2 enhances neural excitability through BK (big potassium) channels | Liu, Na-Na; Xie, Han; Xiang-wei, Wen-Shu; Gao, Kai; Wang, Tian-Shuang; Jiang, Yu-Wu |
| 2016 | Analyses of Genotypes and Phenotypes of Ten Chinese Patients with Wolf-Hirschhorn Syndrome by Multiplex Ligation-dependent Probe Amplification and Array Comparative Genomic Hybridization | Yang, Wen-Xu; Pan, Hong; Li, Lin; Wu, Hai-Rong; Wang, Song-Tao; Bao, Xin-Hua; Jiang, Yu-Wu; Qi, Yu |
| Feb-2020 | Clinical features and surgical outcomes in young children with focal cortical dysplasia type II | Wang, Tian-Shuang; Liu, Qing-Zhu; Liu, Ming; Zhang, Qian; Wang, Ruo-Fan; Wu, Chong-Wei; Zhang, Jie; Wang, Wen; Ji, Tao-Yun; Liu, Xiao-Yan; Wang, Shuang; Cai, Li-Xin; Jiang, Yu-Wu; Wu, Ye |
| 13-Aug-2020 | Current Status, Diagnosis, and Treatment Recommendation for Tic Disorders in China | Liu, Zhi-Sheng; Cui, Yong-Hua; Sun, Dan; Lu, Qing; Jiang, Yu-Wu; Jiang, Li; Wang, Jia-Qin; Luo, Rong; Fang, Fang; Zhou, Shui-Zhen; Wang, Yi; Cai, Fang-Cheng; Lin, Qing; Xiong, Lan; Zheng, Yi; Qin, Jiong |
| 2015 | Different Eukaryotic Initiation Factor 2B epsilon Mutations Lead to Various Degrees of Intolerance to the Stress of Endoplasmic Reticulum in Oligodendrocytes | Chen, Na; Jiang, Yu-Wu; Hao, Hong-Jun; Ban, Ting-Ting; Gao, Kai; Zhang, Zhong-Bin; Wang, Jing-Min; Wu, Ye |
| Jun-2024 | Focal cortical dysplasia II caused by brain somatic mutation of IRS-1 is associated with ERK signaling pathway activation | Li, Xiao; Wang, Tianshuang; Liu, Nana; Cai, Aojie; Zhang, Junjiao; Zhang, Fan; Liu, Qingzhu; Wang, Jingmin; Wu, Ye; Gao, Kai; Jiang, Yu-Wu |
| 2019 | Identification in Chinese patients with GLIALCAM mutations of megalencephalic leukoencephalopathy with subcortical cysts and brain pathological study on Glialcam knock-in mouse models | Shi, Zhen; Yan, Hui-Fang; Cao, Bin-Bin; Guo, Mang-Mang; Xie, Han; Gao, Kai; Xiao, Jiang-Xi; Yang, Yan-Ling; Xiong, Hui; Gu, Qiang; Li, Ming; Wu, Ye; Jiang, Yu-Wu; Wang, Jing-Min |
| 2019 | Modeling vanishing white matter disease with patient-derived induced pluripotent stem cells reveals astrocytic dysfunction | Zhou, Ling; Li, Peng; Chen, Na; Dai, Li-Fang; Gao, Kai; Liu, Yi-Nan; Shen, Li; Wang, Jing-Min; Jiang, Yu-Wu; Wu, Ye |
| 2015 | De Novo KCNMA1 Mutations in Children With Early-Onset Paroxysmal Dyskinesia and Developmental Delay | Zhang, Zhong-Bin; Tian, Mao-Qiang; Gao, Kai; Jiang, Yu-Wu; Wu, Ye |
| Jan-2023 | PACS gene family-related neurological diseases: limited genotypes and diverse phenotypes | Zhang, Han; Gao, Kai; Wang, Shuang; Zhang, Yue-Hua; Yang, Zhi-Xian; Wu, Ye; Jiang, Yu-Wu |
| 20-Jun-2021 | A survey on pediatric anti-N-methyl-D-aspartate-receptor encephalitis treatment strategies in China | Cao, Xiao-Shuang; Kessi, Miriam; Ji, Tao-Yun; Jiang, Yu-Wu; Yin, Fei; Peng, Jing |
| 2013 | Traumatic Scratch Injury in Astrocytes Triggers Calcium Influx to Activate the JNK/c-Jun/AP-1 Pathway and Switch on GFAP Expression | Gao, Kai; Wang, Chen Ran; Jiang, Feng; Wong, Ann Yuen Kwan; Su, Na; Jiang, Jiao Hua; Chai, Rui Chao; Vatcher, Greg; Teng, Junlin; Chen, Jianguo; Jiang, Yu-Wu; Yu, Albert Cheung Hoi |
