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7. Autosomal dominant lateral temporal epilepsy: two families with novel mutations in the LGI1 gene. Hedera P; Abou-Khalil B; Crunk AE; Taylor KA; Haines JL; Sutcliffe JS Epilepsia; 2004 Mar; 45(3):218-22. PubMed ID: 15009222 [TBL] [Abstract][Full Text] [Related]
8. Insights into the mechanisms of epilepsy from structural biology of LGI1-ADAM22. Yamagata A; Fukai S Cell Mol Life Sci; 2020 Jan; 77(2):267-274. PubMed ID: 31432233 [TBL] [Abstract][Full Text] [Related]
9. Two novel epilepsy-linked mutations leading to a loss of function of LGI1. Chabrol E; Popescu C; Gourfinkel-An I; Trouillard O; Depienne C; Senechal K; Baulac M; LeGuern E; Baulac S Arch Neurol; 2007 Feb; 64(2):217-22. PubMed ID: 17296837 [TBL] [Abstract][Full Text] [Related]
10. Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features. Kalachikov S; Evgrafov O; Ross B; Winawer M; Barker-Cummings C; Martinelli Boneschi F; Choi C; Morozov P; Das K; Teplitskaya E; Yu A; Cayanis E; Penchaszadeh G; Kottmann AH; Pedley TA; Hauser WA; Ottman R; Gilliam TC Nat Genet; 2002 Mar; 30(3):335-41. PubMed ID: 11810107 [TBL] [Abstract][Full Text] [Related]
11. A novel LGI1 missense mutation causes dysfunction in cortical neuronal migration and seizures. Liu F; Du C; Tian X; Ma Y; Zhao B; Yan Y; Lin Z; Lin P; Zhou R; Wang X Brain Res; 2019 Oct; 1721():146332. PubMed ID: 31301272 [TBL] [Abstract][Full Text] [Related]
12. LGI1 gene mutation screening in sporadic partial epilepsy with auditory features. Flex E; Pizzuti A; Di Bonaventura C; Douzgou S; Egeo G; Fattouch J; Manfredi M; Dallapiccola B; Giallonardo AT J Neurol; 2005 Jan; 252(1):62-6. PubMed ID: 15654555 [TBL] [Abstract][Full Text] [Related]
13. Similarity of molecular phenotype between known epilepsy gene LGI1 and disease candidate gene LGI2. Limviphuvadh V; Chua LL; Rahim RA; Eisenhaber F; Maurer-Stroh S; Adhikari S BMC Biochem; 2010 Sep; 11():39. PubMed ID: 20863412 [TBL] [Abstract][Full Text] [Related]
16. A newly discovered LGI1 mutation in Korean family with autosomal dominant lateral temporal lobe epilepsy. Lee MK; Kim SW; Lee JH; Cho YJ; Kim DE; Lee BI; Kim HM; Lee MG; Heo K Seizure; 2014 Jan; 23(1):69-73. PubMed ID: 24177143 [TBL] [Abstract][Full Text] [Related]
17. Hyperactive behavior in a family with autosomal dominant lateral temporal lobe epilepsy caused by a mutation in the LGI1/epitempin gene. Berghuis B; Brilstra EH; Lindhout D; Baulac S; de Haan GJ; van Kempen M Epilepsy Behav; 2013 Jul; 28(1):41-6. PubMed ID: 23651915 [TBL] [Abstract][Full Text] [Related]
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19. Epilepsy with auditory features: a LGI1 gene mutation suggests a loss-of-function mechanism. Pizzuti A; Flex E; Di Bonaventura C; Dottorini T; Egeo G; Manfredi M; Dallapiccola B; Giallonardo AT Ann Neurol; 2003 Mar; 53(3):396-9. PubMed ID: 12601709 [TBL] [Abstract][Full Text] [Related]
20. Autosomal dominant epilepsy with auditory features: a new LGI1 family including a phenocopy with cortical dysplasia. Klein KM; Pendziwiat M; Cohen R; Appenzeller S; de Kovel CG; Rosenow F; Koeleman BP; Kuhlenbäumer G; Sheintuch L; Veksler R; Friedman A; Afawi Z; Helbig I J Neurol; 2016 Jan; 263(1):11-6. PubMed ID: 26459092 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]