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浏览/检索结果: 共4条，第1-4条 帮助 已选(0)清除 条数/页：5101520253035404550556065707580859095100   排序方式：请选择作者升序作者降序题名升序题名降序发表日期升序发表日期降序提交时间升序提交时间降序 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. 收藏  |  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