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科研机构
北京大学 [3]
中南大学 [1]
内容类型
期刊论文 [4]
发表日期
2018 [1]
2017 [3]
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Dynamic functional disturbances of brain network in seizure-related cognitive outcomes
期刊论文
Epilepsy Research, 2018, 卷号: 140, 页码: 15-21
作者:
Guo, Jialing
;
Wu, Qian
;
Zhao, Charlie W.
;
Xiao, Bo
;
Feng, Li*
收藏
  |  
浏览/下载:2/0
  |  
提交时间:2019/12/03
BOLD
blood oxygen leveldependent
HFO
high frequency oscillation
FCD
focal cortical dysplasia
IEDs
interictal epileptiform discharges
TCI
transient cognitive impairment
EE
epileptic encephalopathy
NCSE
non-convulsive status epilepticus
ELS
early life seizures
BCECTS
benign childhood epilepsy with centro-temporal spikes
NREM
non-rapid eye movements
AED
anti-epileptic drug
SE
status epilepticus
ESES
electrical status epilepticus during sleep
PPR
photoparoxysmal response
ADSHE
autosomal dominant sleep-related hypermotor epilepsy
Epilepsy
Seizure
Cognition
Spikes
Interictal epileptiform discharges (IEDs)
Blood oxygen level-dependent (BOLD)
Gene mutation analysis of 175 Chinese patients with early-onset epileptic encephalopathy
期刊论文
CLINICAL GENETICS, 2017
Zhang, Q.
;
Li, J.
;
Zhao, Y.
;
Bao, X.
;
Wei, L.
;
Wang, J.
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  |  
浏览/下载:4/0
  |  
提交时间:2017/12/03
CDKL5
early-onset epileptic encephalopathy
KCNQ2
recommending treatment
targeted next-generation sequencing
KCNQ2 ENCEPHALOPATHY
POTASSIUM CHANNEL
CDKL5
SPECTRUM
LOCALIZATION
EPILEPSIES
QUINIDINE
INFANCY
GAIN
SCN8A mutations in Chinese patients with early onset epileptic encephalopathy and benign infantile seizures
期刊论文
BMC MEDICAL GENETICS, 2017
Wang, Jiaping
;
Gao, Hua
;
Bao, Xinhua
;
Zhang, Qingping
;
Li, Jiarui
;
Wei, Liping
;
Wu, Xiru
;
Chen, Yan
;
Yu, Shujie
收藏
  |  
浏览/下载:5/0
  |  
提交时间:2017/12/03
SCN8A
Epileptic encephalopathy
Family cases
DE-NOVO MUTATIONS
SODIUM-CHANNEL
PHENOTYPIC SPECTRUM
CLINICAL SPECTRUM
SCN2A MUTATIONS
RECURRENT
NA(V)1.6
CHILDREN
The clinical spectrum of female epilepsy patients with PCDH19 mutations in a Chinese population
期刊论文
CLINICAL GENETICS, 2017
Liu, A.
;
Xu, X.
;
Yang, X.
;
Jiang, Y.
;
Yang, Z.
;
Liu, X.
;
Wu, Y.
;
Wu, X.
;
Wei, L.
;
Zhang, Y.
收藏
  |  
浏览/下载:8/0
  |  
提交时间:2017/12/04
clinical manifestation
Dravet syndrome
epilepsy
females
fever
PCDH19
PROTOCADHERIN 19 MUTATIONS
MENTAL-RETARDATION
LIMITED EPILEPSY
ONSET EPILEPSY
DE-NOVO
ENCEPHALOPATHY
INHERITANCE
FEVER
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