Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Neuroreport|May 16, 2018
Abnormal expression of ephrin-A5 affects brain development of congenital hypothyroidism ratsGuihai Suo, Feifei Shen, Baolan Sun, et al.
Epilepsy & Behavior : E&B|August 14, 2021
A de novo nonsense mutation of STXBP1 causes early-onset epileptic encephalopathyGuihai Suo, Xing Cao, Yuqin Zheng, et al.
Biochemical and Biophysical Research Communications|November 5, 2017
Profiling neuron-autonomous lncRNA changes upon ischemia/reperfusion injuryHaiying Li, Youjia Wu, Guihai Suo, et al.
IEEE Journal of Biomedical and Health Informatics|April 5, 2022
Whole-Brain Dynamic Resting-State Functional Network Analysis in Benign Epilepsy With Centrotemporal SpikesSiqi Zhang, Jihong Tang, Jing Huang, et al.
BMC Pediatrics|July 2, 2024
Risk factors and predictors of recurrence of febrile seizures in children in Nantong, China: a retrospective cohort studyFeifei Shen, Leijuan Lu, Youjia Wu, et al.
Translational Pediatrics|August 15, 2024
Enhancement of motor neuron development and function in zebrafish by sialyllacto-N-tetraose bPengcheng Li, Peng Chen, Yuqin Zheng, et al.
Cell Death Discovery|December 6, 2022
CaMKIV mediates spine growth deficiency of hippocampal neurons by regulation of EGR3/BDNF signal axis in congenital hypothyroidismHui Wu, Guihai Suo, Tianci Li, et al.
CNS Neuroscience & Therapeutics|September 25, 2025
Congenital Hypothyroidism Dysregulates TRPC6 to Mediate Abnormal Dendritic Spine Growth of Hippocampal NeuronsTianci Li, Feifei Shen, Lingling Li, et al.
Biochemical Pharmacology|July 25, 2024
Preliminary study on the mechanism of SAHA in the treatment of refractory epilepsy induced by GABRG2(F343L) mutationJie Wang, Wenwen Wu, Jiali Wan, et al.
Pageof 1