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9. 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]
10. Screening LGI1 in a cohort of 26 lateral temporal lobe epilepsy patients with auditory aura from Turkey detects a novel de novo mutation. Kesim YF; Uzun GA; Yucesan E; Tuncer FN; Ozdemir O; Bebek N; Ozbek U; Iseri SA; Baykan B Epilepsy Res; 2016 Feb; 120():73-8. PubMed ID: 26773249 [TBL] [Abstract][Full Text] [Related]
11. Autosomal dominant lateral temporal epilepsy (ADLTE): novel structural and single-nucleotide LGI1 mutations in families with predominant visual auras. Dazzo E; Santulli L; Posar A; Fattouch J; Conti S; Lodén-van Straaten M; Mijalkovic J; De Bortoli M; Rosa M; Millino C; Pacchioni B; Di Bonaventura C; Giallonardo AT; Striano S; Striano P; Parmeggiani A; Nobile C Epilepsy Res; 2015 Feb; 110():132-8. PubMed ID: 25616465 [TBL] [Abstract][Full Text] [Related]
12. Analysis of LGI1 promoter sequence, PDYN and GABBR1 polymorphisms in sporadic and familial lateral temporal lobe epilepsy. Bovo G; Diani E; Bisulli F; Di Bonaventura C; Striano P; Gambardella A; Ferlazzo E; Egeo G; Mecarelli O; Elia M; Bianchi A; Bortoluzzi S; Vettori A; Aguglia U; Binelli S; De Falco A; Coppola G; Gobbi G; Sofia V; Striano S; Tinuper P; Giallonardo AT; Michelucci R; Nobile C Neurosci Lett; 2008 May; 436(1):23-6. PubMed ID: 18355961 [TBL] [Abstract][Full Text] [Related]
13. LGI1 is mutated in familial temporal lobe epilepsy characterized by aphasic seizures. Gu W; Brodtkorb E; Steinlein OK Ann Neurol; 2002 Sep; 52(3):364-7. PubMed ID: 12205652 [TBL] [Abstract][Full Text] [Related]
14. A novel loss-of-function LGI1 mutation linked to autosomal dominant lateral temporal epilepsy. Striano P; de Falco A; Diani E; Bovo G; Furlan S; Vitiello L; Pinardi F; Striano S; Michelucci R; de Falco FA; Nobile C Arch Neurol; 2008 Jul; 65(7):939-42. PubMed ID: 18625862 [TBL] [Abstract][Full Text] [Related]
15. Autosomal dominant partial epilepsy with auditory features: a new locus on chromosome 19q13.11-q13.31. Bisulli F; Naldi I; Baldassari S; Magini P; Licchetta L; Castegnaro G; Fabbri M; Stipa C; Ferrari S; Seri M; Gonçalves Silva GE; Tinuper P; Pippucci T Epilepsia; 2014 Jun; 55(6):841-8. PubMed ID: 24579982 [TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. ADPEAF mutations reduce levels of secreted LGI1, a putative tumor suppressor protein linked to epilepsy. Senechal KR; Thaller C; Noebels JL Hum Mol Genet; 2005 Jun; 14(12):1613-20. PubMed ID: 15857855 [TBL] [Abstract][Full Text] [Related]
19. A rat model for LGI1-related epilepsies. Baulac S; Ishida S; Mashimo T; Boillot M; Fumoto N; Kuwamura M; Ohno Y; Takizawa A; Aoto T; Ueda M; Ikeda A; LeGuern E; Takahashi R; Serikawa T Hum Mol Genet; 2012 Aug; 21(16):3546-57. PubMed ID: 22589250 [TBL] [Abstract][Full Text] [Related]
20. Penetrance of LGI1 mutations in autosomal dominant partial epilepsy with auditory features. Rosanoff MJ; Ottman R Neurology; 2008 Aug; 71(8):567-71. PubMed ID: 18711109 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]