243 related articles for article (PubMed ID: 19818940)
1. Novel mutation in KCNQ2 causing benign familial neonatal seizures.
Goldberg-Stern H; Kaufmann R; Kivity S; Afawi Z; Heron SE
Pediatr Neurol; 2009 Nov; 41(5):367-70. PubMed ID: 19818940
[TBL] [Abstract][Full Text] [Related]
2. KCNQ2 and KCNQ3 mutations contribute to different idiopathic epilepsy syndromes.
Neubauer BA; Waldegger S; Heinzinger J; Hahn A; Kurlemann G; Fiedler B; Eberhard F; Muhle H; Stephani U; Garkisch S; Eeg-Olofsson O; Müller U; Sander T
Neurology; 2008 Jul; 71(3):177-83. PubMed ID: 18625963
[TBL] [Abstract][Full Text] [Related]
3. 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]
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]
5. Electroconvulsive seizure thresholds and kindling acquisition rates are altered in mouse models of human KCNQ2 and KCNQ3 mutations for benign familial neonatal convulsions.
Otto JF; Singh NA; Dahle EJ; Leppert MF; Pappas CM; Pruess TH; Wilcox KS; White HS
Epilepsia; 2009 Jul; 50(7):1752-9. PubMed ID: 19453707
[TBL] [Abstract][Full Text] [Related]
6. Genetic testing in benign familial epilepsies of the first year of life: clinical and diagnostic significance.
Zara F; Specchio N; Striano P; Robbiano A; Gennaro E; Paravidino R; Vanni N; Beccaria F; Capovilla G; Bianchi A; Caffi L; Cardilli V; Darra F; Bernardina BD; Fusco L; Gaggero R; Giordano L; Guerrini R; Incorpora G; Mastrangelo M; Spaccini L; Laverda AM; Vecchi M; Vanadia F; Veggiotti P; Viri M; Occhi G; Budetta M; Taglialatela M; Coviello DA; Vigevano F; Minetti C
Epilepsia; 2013 Mar; 54(3):425-36. PubMed ID: 23360469
[TBL] [Abstract][Full Text] [Related]
7. A novel missense mutation (N258S) in the KCNQ2 gene in a Turkish family afflicted with benign familial neonatal convulsions (BFNC).
Yalçin O; Cağlayan SH; Saltik S; Cokar O; Ağan K; Dervent A; Steinlein OK
Turk J Pediatr; 2007; 49(4):385-9. PubMed ID: 18246739
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Benign familial neonatal convulsions: novel mutation in a newborn.
Lee IC; Chen JY; Chen YJ; Yu JS; Su PH
Pediatr Neurol; 2009 May; 40(5):387-91. PubMed ID: 19380078
[TBL] [Abstract][Full Text] [Related]
10. [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]
11. 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]
12. Functional analysis of novel KCNQ2 mutations found in patients with Benign Familial Neonatal Convulsions.
Volkers L; Rook MB; Das JH; Verbeek NE; Groenewegen WA; van Kempen MJ; Lindhout D; Koeleman BP
Neurosci Lett; 2009 Oct; 462(1):24-9. PubMed ID: 19559753
[TBL] [Abstract][Full Text] [Related]
13. Novel KCNQ2 mutation in a large Emirati family with benign familial neonatal seizures.
Saadeldin IY; Milhem RM; Al-Gazali L; Ali BR
Pediatr Neurol; 2013 Jan; 48(1):63-6. PubMed ID: 23290024
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Sodium and potassium channel dysfunctions in rare and common idiopathic epilepsy syndromes.
Hahn A; Neubauer BA
Brain Dev; 2009 Aug; 31(7):515-20. PubMed ID: 19464834
[TBL] [Abstract][Full Text] [Related]
16. [Benign familial neonatal convulsions: a model of idiopathic epilepsy].
Hirsch E; de Saint-Martin A; Marescaux C
Rev Neurol (Paris); 1999 Jul; 155(6-7):463-7. PubMed ID: 10472660
[TBL] [Abstract][Full Text] [Related]
17. Developmental changes in KCNQ2 and KCNQ3 expression in human brain: possible contribution to the age-dependent etiology of benign familial neonatal convulsions.
Kanaumi T; Takashima S; Iwasaki H; Itoh M; Mitsudome A; Hirose S
Brain Dev; 2008 May; 30(5):362-9. PubMed ID: 18166285
[TBL] [Abstract][Full Text] [Related]
18. Deletions or duplications in KCNQ2 can cause benign familial neonatal seizures.
Heron SE; Cox K; Grinton BE; Zuberi SM; Kivity S; Afawi Z; Straussberg R; Berkovic SF; Scheffer IE; Mulley JC
J Med Genet; 2007 Dec; 44(12):791-6. PubMed ID: 17675531
[TBL] [Abstract][Full Text] [Related]
19. [Clinical and mutational analysis of KCNQ3 gene in a Chinese family with benign familial neonatal convulsions].
Li HY; Tang BS; Yan XX; Guo JF; Shen L; Song YM; Jiang H; Xia K; Xie ZG; Yang QA
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Aug; 23(4):374-7. PubMed ID: 16883520
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
