These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
258 related articles for article (PubMed ID: 15079011)
41. Autosomal dominant nocturnal frontal lobe epilepsy. A video-polysomnographic and genetic appraisal of 40 patients and delineation of the epileptic syndrome. Oldani A; Zucconi M; Asselta R; Modugno M; Bonati MT; Dalprà L; Malcovati M; Tenchini ML; Smirne S; Ferini-Strambi L Brain; 1998 Feb; 121 ( Pt 2)():205-23. PubMed ID: 9549500 [TBL] [Abstract][Full Text] [Related]
42. Familial partial epilepsy with variable foci in a Dutch family: clinical characteristics and confirmation of linkage to chromosome 22q. Callenbach PM; van den Maagdenberg AM; Hottenga JJ; van den Boogerd EH; de Coo RF; Lindhout D; Frants RR; Sandkuijl LA; Brouwer OF Epilepsia; 2003 Oct; 44(10):1298-305. PubMed ID: 14510823 [TBL] [Abstract][Full Text] [Related]
43. 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]
45. Childhood absence epilepsy and febrile seizures: a family with a GABA(A) receptor mutation. Marini C; Harkin LA; Wallace RH; Mulley JC; Scheffer IE; Berkovic SF Brain; 2003 Jan; 126(Pt 1):230-40. PubMed ID: 12477709 [TBL] [Abstract][Full Text] [Related]
46. [Clinical features in a Japanese patient with autosomal dominant lateral temporal epilepsy having LGI1 mutation]. Fujita Y; Ikeda A; Kadono K; Kawamata J; Tomimoto H; Fukuyama H; Takahashi R Rinsho Shinkeigaku; 2009 Apr; 49(4):186-90. PubMed ID: 19462817 [TBL] [Abstract][Full Text] [Related]
47. 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]
48. 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]
49. 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]
58. Low penetrance and effect on protein secretion of LGI1 mutations causing autosomal dominant lateral temporal epilepsy. Di Bonaventura C; Operto FF; Busolin G; Egeo G; D'Aniello A; Vitello L; Smaniotto G; Furlan S; Diani E; Michelucci R; Giallonardo AT; Coppola G; Nobile C Epilepsia; 2011 Jul; 52(7):1258-64. PubMed ID: 21504429 [TBL] [Abstract][Full Text] [Related]
59. 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]
60. Exclusion of linkage of genetic focal sharp waves to the HLA region on chromosome 6p in families with benign partial epilepsy with centrotemporal sharp waves. Whitehouse W; Diebold U; Rees M; Parker K; Doose H; Gardiner RM Neuropediatrics; 1993 Aug; 24(4):208-10. PubMed ID: 8232778 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]