Genetic and molecular basis of epilepsy-related cognitive dysfunction

Author:

Zhu Lin,Chen Lu,Xu Puying,Lu Di,Dai Shujuan,Zhong Lianmei,Han Yanbing,Zhang Mengqi,Xiao Bo,Chang Lvhua,Wu Qian

Funder

National Natural Science Foundation of China

Yunnan Applied Basic Research Projects

Natural Science Foundation of Hunan Province

Yunnan Provincial Key Projects

Program for Science and Technology Innovation Team in Kunming Medical University

China Scholarship Council

Publisher

Elsevier BV

Subject

Behavioral Neuroscience,Clinical Neurology,Neurology

Reference270 articles.

1. Epilepsy in adults;Thijs;Lancet,2019

2. The level of neuregulin-1 after traumatic brain injury and formation of post-traumatic epilepsy;Gazaryan;Bull Exp Biol Med,2019

3. Seizures in pediatric patients with primary brain tumors;Robert-Boire;Pediatr Neurol,2019

4. A novel CCM1/KRIT1 heterozygous nonsense mutation (c.1864C>T) associated with familial cerebral cavernous malformation: a genetic insight from an 8-year continuous observational study;Yang;J Mol Neurosci,2017

5. Myotonia permanens with Nav1.4-G1306E displays varied phenotypes during course of life;Lehmann-Horn;Acta Myol,2017

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