• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Structural anomaly of left lateral temporal lobe in epilepsy due to mutated LGI1.

作者信息

Tessa C, Michelucci R, Nobile C, Giannelli M, Della Nave R, Testoni S, Bianucci D, Tinuper P, Bisulli F, Sofia V, De Feo M R, Giallonardo A T, Tassinari C A, Mascalchi M

机构信息

Radiologia, Ospedale della Versilia, Pietrasanta, Lucca, Italy.

出版信息

Neurology. 2007 Sep 18;69(12):1298-300. doi: 10.1212/01.wnl.0000277045.16688.b6.

DOI:10.1212/01.wnl.0000277045.16688.b6
PMID:17875918
Abstract
摘要

相似文献

1
Structural anomaly of left lateral temporal lobe in epilepsy due to mutated LGI1.由于LGI1基因突变导致的癫痫中左侧颞叶的结构异常。
Neurology. 2007 Sep 18;69(12):1298-300. doi: 10.1212/01.wnl.0000277045.16688.b6.
2
Familial mesial temporal lobe epilepsy (FMTLE) : a clinical and genetic study of 15 Italian families.家族性内侧颞叶癫痫(FMTLE):对15个意大利家庭的临床与遗传学研究
J Neurol. 2008 Jan;255(1):16-23. doi: 10.1007/s00415-007-0653-1. Epub 2007 Nov 21.
3
Low penetrance of autosomal dominant lateral temporal epilepsy in Italian families without LGI1 mutations.常染色体显性外侧颞叶癫痫在无 LGI1 突变的意大利家族中的低外显率。
Epilepsia. 2013 Jul;54(7):1288-97. doi: 10.1111/epi.12194. Epub 2013 Apr 26.
4
A novel loss-of-function LGI1 mutation linked to autosomal dominant lateral temporal epilepsy.一种与常染色体显性外侧颞叶癫痫相关的新型功能丧失性LGI1突变。
Arch Neurol. 2008 Jul;65(7):939-42. doi: 10.1001/archneur.65.7.939.
5
Low penetrance and effect on protein secretion of LGI1 mutations causing autosomal dominant lateral temporal epilepsy.LGI1 基因突变导致常染色体显性颞叶外侧癫痫的低外显率和对蛋白质分泌的影响。
Epilepsia. 2011 Jul;52(7):1258-64. doi: 10.1111/j.1528-1167.2011.03071.x. Epub 2011 Apr 19.
6
Abnormal phonologic processing in familial lateral temporal lobe epilepsy due to a new LGI1 mutation.因一种新的LGI1突变导致的家族性外侧颞叶癫痫中的异常语音处理。
Epilepsia. 2005 Jan;46(1):118-23. doi: 10.1111/j.0013-9580.2005.26304.x.
7
LGI1 gene mutation screening in sporadic partial epilepsy with auditory features.伴有听觉特征的散发性部分性癫痫中LGI1基因突变筛查
J Neurol. 2005 Jan;252(1):62-6. doi: 10.1007/s00415-005-0599-0.
8
A newly discovered LGI1 mutation in Korean family with autosomal dominant lateral temporal lobe epilepsy.一个新发现的 LGI1 突变与韩国常染色体显性外侧颞叶癫痫家系相关。
Seizure. 2014 Jan;23(1):69-73. doi: 10.1016/j.seizure.2013.10.001. Epub 2013 Oct 12.
9
Mutations in LGI1 gene in Japanese families with autosomal dominant lateral temporal lobe epilepsy: the first report from Asian families.LGI1 基因突变致常染色体显性遗传性颞叶外侧癫痫:亚洲家族的首例报告。
Epilepsia. 2010 Apr;51(4):690-3. doi: 10.1111/j.1528-1167.2009.02309.x. Epub 2009 Sep 22.
10
Idiopathic mesial temporal lobe epilepsy: a syndrome with complex inheritance?
J Neurol. 2009 Dec;256(12):2104-5. doi: 10.1007/s00415-009-5313-1. Epub 2009 Sep 11.

引用本文的文献

1
Cortical metabolic characteristics of anti-leucine-rich glioma-inactivated 1 antibody encephalitis based on F-FDG PET.基于F-FDG PET的抗富含亮氨酸胶质瘤失活1抗体脑炎的皮质代谢特征
Front Neurol. 2023 Mar 31;14:1100760. doi: 10.3389/fneur.2023.1100760. eCollection 2023.
2
Imaging Genetics in Epilepsy: Current Knowledge and New Perspectives.癫痫的影像遗传学:当前认知与新视角
Front Mol Neurosci. 2022 May 30;15:891621. doi: 10.3389/fnmol.2022.891621. eCollection 2022.
3
Epilepsy With Auditory Features: From Etiology to Treatment.
具有听觉特征的癫痫:从病因到治疗
Front Neurol. 2022 Jan 27;12:807939. doi: 10.3389/fneur.2021.807939. eCollection 2021.
4
LGI1 expression and human brain asymmetry: insights from patients with LGI1-antibody encephalitis.LGI1 表达与人类大脑的不对称性:来自 LGI1 抗体脑炎患者的见解。
J Neuroinflammation. 2018 Sep 25;15(1):279. doi: 10.1186/s12974-018-1314-2.
5
Seizures and Epilepsies due to Channelopathies and Neurotransmitter Receptor Dysfunction: A Parallel between Genetic and Immune Aspects.离子通道病和神经递质受体功能障碍所致癫痫发作与癫痫:遗传与免疫方面的平行关系
Mol Syndromol. 2016 Sep;7(4):197-209. doi: 10.1159/000447707. Epub 2016 Jul 22.
6
Autoimmune synaptopathies.自身免疫性突触病。
Nat Rev Neurosci. 2016 Feb;17(2):103-17. doi: 10.1038/nrn.2015.27.
7
Autosomal dominant epilepsy with auditory features: a new LGI1 family including a phenocopy with cortical dysplasia.具有听觉特征的常染色体显性遗传性癫痫:一个新的LGI1基因家族,包括一例伴有皮质发育异常的表型模拟病例。
J Neurol. 2016 Jan;263(1):11-6. doi: 10.1007/s00415-015-7921-2. Epub 2015 Oct 12.
8
LGI Proteins and Epilepsy in Human and Animals.LGI蛋白与人和动物的癫痫
J Vet Intern Med. 2015 Jul-Aug;29(4):997-1005. doi: 10.1111/jvim.12610. Epub 2015 Jun 1.
9
Homozygous Deletion of the LGI1 Gene in Mice Leads to Developmental Abnormalities Resulting in Cortical Dysplasia.小鼠中LGI1基因的纯合缺失导致发育异常,进而引起皮质发育异常。
Brain Pathol. 2015 Sep;25(5):587-97. doi: 10.1111/bpa.12225. Epub 2014 Dec 1.
10
LGI proteins in the nervous system.神经系统中的 LGI 蛋白。
ASN Neuro. 2013 Jun 25;5(3):167-81. doi: 10.1042/AN20120095.