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6. A Kv4.2 truncation mutation in a patient with temporal lobe epilepsy. Singh B; Ogiwara I; Kaneda M; Tokonami N; Mazaki E; Baba K; Matsuda K; Inoue Y; Yamakawa K Neurobiol Dis; 2006 Nov; 24(2):245-53. PubMed ID: 16934482 [TBL] [Abstract][Full Text] [Related]
7. Structural anomaly of left lateral temporal lobe in epilepsy due to mutated LGI1. Tessa C; Michelucci R; Nobile C; Giannelli M; Della Nave R; Testoni S; Bianucci D; Tinuper P; Bisulli F; Sofia V; De Feo MR; Giallonardo AT; Tassinari CA; Mascalchi M Neurology; 2007 Sep; 69(12):1298-300. PubMed ID: 17875918 [No Abstract] [Full Text] [Related]
8. Mutations and polymorphisms of the CLCN2 gene in idiopathic epilepsy. D'Agostino D; Bertelli M; Gallo S; Cecchin S; Albiero E; Garofalo PG; Gambardella A; St Hilaire JM; Kwiecinski H; Andermann E; Pandolfo M Neurology; 2004 Oct; 63(8):1500-2. PubMed ID: 15505175 [TBL] [Abstract][Full Text] [Related]
9. 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]
10. Late-onset childhood occipital epilepsy (Gastaut type): a family study. Grosso S; Vivarelli R; Gobbi G; Di Bartolo R; Berardi R; Balestri P Eur J Paediatr Neurol; 2008 Sep; 12(5):421-6. PubMed ID: 18249143 [TBL] [Abstract][Full Text] [Related]
11. 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]
12. Seizure semiology in autosomal dominant epilepsy with auditory features, due to novel LGI1 mutations. Sadleir LG; Agher D; Chabrol E; Elkouby L; Leguern E; Paterson SJ; Harty R; Bellows ST; Berkovic SF; Scheffer IE; Baulac S Epilepsy Res; 2013 Dec; 107(3):311-7. PubMed ID: 24206907 [TBL] [Abstract][Full Text] [Related]
13. A novel inherited mutation in the voltage sensor region of SCN1A is associated with Panayiotopoulos syndrome in siblings and generalized epilepsy with febrile seizures plus. Livingston JH; Cross JH; Mclellan A; Birch R; Zuberi SM J Child Neurol; 2009 Apr; 24(4):503-8. PubMed ID: 19339291 [TBL] [Abstract][Full Text] [Related]
14. 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]
15. Genetics of the epilepsies. Gutierrez-Delicado E; Serratosa JM Curr Opin Neurol; 2004 Apr; 17(2):147-53. PubMed ID: 15021241 [TBL] [Abstract][Full Text] [Related]
16. Low penetrance of autosomal dominant lateral temporal epilepsy in Italian families without LGI1 mutations. Michelucci R; Pasini E; Malacrida S; Striano P; Bonaventura CD; Pulitano P; Bisulli F; Egeo G; Santulli L; Sofia V; Gambardella A; Elia M; de Falco A; Neve Al; Banfi P; Coppola G; Avoni P; Binelli S; Boniver C; Pisano T; Marchini M; Dazzo E; Fanciulli M; Bartolini Y; Riguzzi P; Volpi L; de Falco FA; Giallonardo AT; Mecarelli O; Striano S; Tinuper P; Nobile C Epilepsia; 2013 Jul; 54(7):1288-97. PubMed ID: 23621105 [TBL] [Abstract][Full Text] [Related]
17. Speech-induced aphasic seizures in epilepsy caused by LGI1 mutation. Brodtkorb E; Michler RP; Gu W; Steinlein OK Epilepsia; 2005 Jun; 46(6):963-6. PubMed ID: 15946341 [TBL] [Abstract][Full Text] [Related]
18. Late onset familial Alzheimer's disease: novel presenilin 2 mutation and PS1 E318G polymorphism. Bernardi L; Tomaino C; Anfossi M; Gallo M; Geracitano S; Puccio G; Colao R; Frangipane F; Mirabelli M; Smirne N; Maletta RG; Bruni AC J Neurol; 2008 Apr; 255(4):604-6. PubMed ID: 18350357 [No Abstract] [Full Text] [Related]
19. 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]
20. Mutation of sodium channel SCN3A in a patient with cryptogenic pediatric partial epilepsy. Holland KD; Kearney JA; Glauser TA; Buck G; Keddache M; Blankston JR; Glaaser IW; Kass RS; Meisler MH Neurosci Lett; 2008 Mar; 433(1):65-70. PubMed ID: 18242854 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]