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2. A KCNQ2 splice site mutation causing benign neonatal convulsions in a Scottish family. Lee WL; Biervert C; Hallmann K; Tay A; Dean JC; Steinlein OK Neuropediatrics; 2000 Feb; 31(1):9-12. PubMed ID: 10774989 [TBL] [Abstract][Full Text] [Related]
3. Atypical gating of M-type potassium channels conferred by mutations in uncharged residues in the S4 region of KCNQ2 causing benign familial neonatal convulsions. Soldovieri MV; Cilio MR; Miceli F; Bellini G; Miraglia del Giudice E; Castaldo P; Hernandez CC; Shapiro MS; Pascotto A; Annunziato L; Taglialatela M J Neurosci; 2007 May; 27(18):4919-28. PubMed ID: 17475800 [TBL] [Abstract][Full Text] [Related]
4. KCNQ2 and KCNQ3 potassium channel genes in benign familial neonatal convulsions: expansion of the functional and mutation spectrum. Singh NA; Westenskow P; Charlier C; Pappas C; Leslie J; Dillon J; Anderson VE; Sanguinetti MC; Leppert MF; Brain; 2003 Dec; 126(Pt 12):2726-37. PubMed ID: 14534157 [TBL] [Abstract][Full Text] [Related]
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6. Benign familial neonatal convulsions caused by altered gating of KCNQ2/KCNQ3 potassium channels. Castaldo P; del Giudice EM; Coppola G; Pascotto A; Annunziato L; Taglialatela M J Neurosci; 2002 Jan; 22(2):RC199. PubMed ID: 11784811 [TBL] [Abstract][Full Text] [Related]
7. A novel mutation in KCNQ2 gene causes benign familial neonatal convulsions in a Chinese family. Tang B; Li H; Xia K; Jiang H; Pan Q; Shen L; Long Z; Zhao G; Cai F J Neurol Sci; 2004 Jun; 221(1-2):31-4. PubMed ID: 15178210 [TBL] [Abstract][Full Text] [Related]
8. The voltage gated potassium channel KCNQ2 and idiopathic generalized epilepsy. Steinlein OK; Stoodt J; Biervert C; Janz D; Sander T Neuroreport; 1999 Apr; 10(6):1163-6. PubMed ID: 10363917 [TBL] [Abstract][Full Text] [Related]
9. Familial neonatal seizures in 36 families: Clinical and genetic features correlate with outcome. Grinton BE; Heron SE; Pelekanos JT; Zuberi SM; Kivity S; Afawi Z; Williams TC; Casalaz DM; Yendle S; Linder I; Lev D; Lerman-Sagie T; Malone S; Bassan H; Goldberg-Stern H; Stanley T; Hayman M; Calvert S; Korczyn AD; Shevell M; Scheffer IE; Mulley JC; Berkovic SF Epilepsia; 2015 Jul; 56(7):1071-80. PubMed ID: 25982755 [TBL] [Abstract][Full Text] [Related]
10. A de novo KCNQ2 mutation detected in non-familial benign neonatal convulsions. Ishii A; Fukuma G; Uehara A; Miyajima T; Makita Y; Hamachi A; Yasukochi M; Inoue T; Yasumoto S; Okada M; Kaneko S; Mitsudome A; Hirose S Brain Dev; 2009 Jan; 31(1):27-33. PubMed ID: 18640800 [TBL] [Abstract][Full Text] [Related]
11. [A novel mutation of KCNQ2 gene in a Chinese family with benign familial neonatal convulsions]. Li HY; Tang BS; Zhang AM; Cao QH; Meng GL; Jiang H; Shen L Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Dec; 20(6):482-5. PubMed ID: 14669214 [TBL] [Abstract][Full Text] [Related]
12. [A novel mutation in KCNQ2 gene causes benign familial infantile convulsions (BFIC) in a Chinese family]. Zhou XH; Ma AQ; Liu XH; Huang C; Zhang YM; Shi RM Zhonghua Er Ke Za Zhi; 2006 Jul; 44(7):487-91. PubMed ID: 17044971 [TBL] [Abstract][Full Text] [Related]
13. De novo KCNQ2 mutations in patients with benign neonatal seizures. Claes LR; Ceulemans B; Audenaert D; Deprez L; Jansen A; Hasaerts D; Weckx S; Claeys KG; Del-Favero J; Van Broeckhoven C; De Jonghe P Neurology; 2004 Dec; 63(11):2155-8. PubMed ID: 15596769 [TBL] [Abstract][Full Text] [Related]
14. The voltage-gated potassium channel KCNQ2 in Taiwanese children with febrile convulsions. Chou IC; Tsai FJ; Huang CC; Lin CC; Tsai CH Neuroreport; 2002 Oct; 13(15):1971-3. PubMed ID: 12395102 [TBL] [Abstract][Full Text] [Related]
15. M-channels: neurological diseases, neuromodulation, and drug development. Cooper EC; Jan LY Arch Neurol; 2003 Apr; 60(4):496-500. PubMed ID: 12707061 [TBL] [Abstract][Full Text] [Related]
16. Benign familial neonatal convulsions caused by mutation in KCNQ3, exon 6: a European case. Fister P; Soltirovska-Salamon A; Debeljak M; Paro-Panjan D Eur J Paediatr Neurol; 2013 May; 17(3):308-10. PubMed ID: 23146207 [TBL] [Abstract][Full Text] [Related]
17. Genes and mutations in idiopathic epilepsy. Steinlein OK Am J Med Genet; 2001; 106(2):139-45. PubMed ID: 11579434 [TBL] [Abstract][Full Text] [Related]
18. Complete loss of the cytoplasmic carboxyl terminus of the KCNQ2 potassium channel: a novel mutation in a large Czech pedigree with benign neonatal convulsions or other epileptic phenotypes. Pereira S; Roll P; Krizova J; Genton P; Brazdil M; Kuba R; Cau P; Rektor I; Szepetowski P Epilepsia; 2004 Apr; 45(4):384-90. PubMed ID: 15030501 [TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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] [Next] [New Search]