Chinese Journal of Contemporary Neurology and Neurosurgery - Digital Cluster of Scitech Periodicals

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Chinese Journal of Contemporary Neurology and Neurosurgery

ISTIC

PKU

ISSN：1672-6731

CN：12-1363/R

Frequency：Monthly

Website：none

Email：xdsjjbzz@263.net.cn

Postcode：300350

Articles4438

Citations29583

Funded1096

Impact Factor：1.37

Articles

2025 No.11

Total 15 articles

Special Topic

Key research breakthroughs in epilepsy of 2024WANG Qun, SHAO Xiao-qiu

979-985

Standard and Guidelines

Chinese expert consensus on disclosure of sudden unexpected death in epilepsyComorbidity Committee of China Association Against Epilepsy, LIU Yong-hong, LI Jin-mei, WANG Qun

986-991

Special Review

Progress on resting-state electroencephalography functional connectivity based on graph theory in epilepsyQIN Xiao-xiao, WANG Qun

992-998

Childhood Epilepsy

Application of cerebrospinal fluid/serum albumin ratio in assessing blood-brain barrier permeability in children with drug-resistant epilepsyWANG Yao, MA Wei, CAI Ao-jie, JIN Pei-na, ZHUO Zhi-hong, WANG Huai-li

999-1003

Analysis of risk factors for cluster seizures in children with epilepsy and construction of a Nomogram modelFANG Jie, WANG Xin-ru, LU Yuan-hang, LI Rui, QU Rui, DAI Yuan-yuan

1004-1011

Lennox-Gastaut syndrome caused by CHD2 gene de novo variation:three cases report and literature reviewNIU Yue, ZHOU Zong-pu, JIAO Xian-ru, XU Zhao, QIN Jiong, YANG Zhi-xian

1012-1019

Developmental and epileptic encephalopathy type 96 caused by de novo variation in NSF gene:one case report and literature reviewXU Jia-xuan, TANG Han-lin, KONG Qing-xia, LI Qiu-bo, JIANG Xiu-fang

1020-1026

Epilepsy Related Disorder

Lissencephaly spectrum disorders caused by CEP85L gene variation:one case report and literature reviewLIU Zhao-xia, ZUO Jing-wen, DAI Ying-yue, ZHANG Jia-ying, SHAO Xiao-qiu, WANG Qun, LÜ Rui-juan

1027-1033

Risk factors for epilepsy recurrence in anti-N-methyl-D-aspartate receptor encephalitis patients with epileptic seizureWANG Xue, LIU Xiao, WANG Qun

1034-1039

Neurological Rare Diseases

Limb-girdle muscular dystrophy type 2A with normal Calpain-3 expression caused by a homozygous mutation in CAPN3 gene:one case reportYANG Yu-fang, LIANG Tao, SHI Chao, YAN Lin-lin, XU Zu-cai, LUO Zhong

1040-1045