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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 Data on mutations and Clinical features in SCN1A or SCN2A gene 期刊论文 DATA IN BRIEF, 2019, 卷号: 22 作者:  Kong, Yanting;  Yan, Kai;  Hu, Liyuan;  Wang, Mingbang;  Dong, Xinran 收藏  |  浏览/下载：29/0  |  提交时间：2019/12/05 Association between SCN1A and SCN2A mutations and clinical/EEG features in Chinese patients from epilepsy or severe seizures 期刊论文 CLINICA CHIMICA ACTA, 2018, 卷号: 483 作者:  Kong, Yanting;  Yan, Kai;  Hu, Liyuan;  Wang, Mingbang;  Dong, Xinran 收藏  |  浏览/下载：3/0  |  提交时间：2019/12/05 SCN1A  SCN2A  Epilepsy  Genotype  Phenotype   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   Partial epilepsy with antecedent febrile seizures and seizure aggravation by antiepileptic drugs: Associated with loss of function of Na(v)1.1 期刊论文 EPILEPSIA, 2010, 卷号: 51, 期号: 9, 页码: 1669-1678 Liao, Wei-Ping; Shi, Yi-Wu; Long, Yue-Sheng; Zeng, Yang; Li, Tian; Yu, Mei-Juan; Su, Tao; Deng, Ping; Lei, Zhi-Gang; Xu, Shu-Jun; Deng, Wei-Yi; Liu, Xiao-Rong; Sun, Wei-Wen; Yi, Yong-Hong; Xu, Zao C.; Duan, Shumin 收藏  |  浏览/下载：51/0  |  提交时间：2012/07/13 SCN1A  Channelopathy  Partial epilepsy  Febrile seizures  Sodium channel  SEVERE MYOCLONIC EPILEPSY  NEURONAL SODIUM-CHANNEL  FAMILIAL HEMIPLEGIC MIGRAINE  TEMPORAL-LOBE EPILEPSY  GENERALIZED EPILEPSY  SCN1A MUTATIONS  NA+ CHANNEL  GENE SCN1A  INFANCY  PLUS