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29. A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family. Charlier C; Singh NA; Ryan SG; Lewis TB; Reus BE; Leach RJ; Leppert M Nat Genet; 1998 Jan; 18(1):53-5. PubMed ID: 9425900 [TBL] [Abstract][Full Text] [Related]
30. Benign childhood epilepsy with centrotemporal spikes and electroencephalography trait are not linked to EBN1 and EBN2 of benign neonatal familial convulsions. Neubauer BA; Moises HW; Lässker U; Waltz S; Diebold U; Stephani U Epilepsia; 1997 Jul; 38(7):782-7. PubMed ID: 9579905 [TBL] [Abstract][Full Text] [Related]
31. A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns. Singh NA; Charlier C; Stauffer D; DuPont BR; Leach RJ; Melis R; Ronen GM; Bjerre I; Quattlebaum T; Murphy JV; McHarg ML; Gagnon D; Rosales TO; Peiffer A; Anderson VE; Leppert M Nat Genet; 1998 Jan; 18(1):25-9. PubMed ID: 9425895 [TBL] [Abstract][Full Text] [Related]
32. Myokymia and neonatal epilepsy caused by a mutation in the voltage sensor of the KCNQ2 K+ channel. Dedek K; Kunath B; Kananura C; Reuner U; Jentsch TJ; Steinlein OK Proc Natl Acad Sci U S A; 2001 Oct; 98(21):12272-7. PubMed ID: 11572947 [TBL] [Abstract][Full Text] [Related]
33. [Molecular defects may cause epilepsy. New discoveries can provide better possibilities for directional diagnostics and treatment]. Brismar T Lakartidningen; 2000 Nov; 97(45):5102-6. PubMed ID: 11116887 [TBL] [Abstract][Full Text] [Related]
34. KCNQ2 abnormality in BECTS: benign childhood epilepsy with centrotemporal spikes following benign neonatal seizures resulting from a mutation of KCNQ2. Ishii A; Miyajima T; Kurahashi H; Wang JW; Yasumoto S; Kaneko S; Hirose S Epilepsy Res; 2012 Nov; 102(1-2):122-5. PubMed ID: 22884718 [TBL] [Abstract][Full Text] [Related]
35. Familial pericentric inversion of chromosome 5 in a family with benign neonatal convulsions. Concolino D; Iembo MA; Rossi E; Giglio S; Coppola G; Miraglia Del Giudice E; Strisciuglio P J Med Genet; 2002 Mar; 39(3):214-6. PubMed ID: 11897828 [No Abstract] [Full Text] [Related]
38. Homozygous deletion in KVLQT1 associated with Jervell and Lange-Nielsen syndrome. Chen Q; Zhang D; Gingell RL; Moss AJ; Napolitano C; Priori SG; Schwartz PJ; Kehoe E; Robinson JL; Schulze-Bahr E; Wang Q; Towbin JA Circulation; 1999 Mar; 99(10):1344-7. PubMed ID: 10077519 [TBL] [Abstract][Full Text] [Related]
39. Evidence of a third locus for benign familial convulsions. Lewis TB; Shevell MI; Andermann E; Ryan SG; Leach RJ J Child Neurol; 1996 May; 11(3):211-4. PubMed ID: 8734025 [TBL] [Abstract][Full Text] [Related]
40. Deletions involving both KCNQ2 and CHRNA4 present with benign familial neonatal seizures. Kurahashi H; Wang JW; Ishii A; Kojima T; Wakai S; Kizawa T; Fujimoto Y; Kikkawa K; Yoshimura K; Inoue T; Yasumoto S; Ogawa A; Kaneko S; Hirose S Neurology; 2009 Oct; 73(15):1214-7. PubMed ID: 19822871 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]