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Journal Abstract Search

156 related items for PubMed ID: 23146207

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  • 2. A novel mutation of KCNQ3 gene in a Chinese family with benign familial neonatal convulsions.
    Li H, Li N, Shen L, Jiang H, Yang Q, Song Y, Guo J, Xia K, Pan Q, Tang B.
    Epilepsy Res; 2008 Mar; 79(1):1-5. PubMed ID: 18249525
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  • 6. 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 Mar; 49(4):385-9. PubMed ID: 18246739
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  • 7. 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
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  • 9. [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
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  • 11. Role of KCNQ2 and KCNQ3 genes in juvenile idiopathic epilepsy in Arabian foals.
    Lichter-Peled A, Polani S, Stanyon R, Rocchi M, Kahila Bar-Gal G.
    Vet J; 2013 Apr; 196(1):57-63. PubMed ID: 23182620
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  • 12. 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
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  • 13. 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 02; 462(1):24-9. PubMed ID: 19559753
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  • 15. 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 02; 31(1):9-12. PubMed ID: 10774989
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  • 17. The first Korean case of KCNQ2 mutation in a family with benign familial neonatal convulsions.
    Yum MS, Ko TS, Yoo HW.
    J Korean Med Sci; 2010 Feb 02; 25(2):324-6. PubMed ID: 20119593
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  • 20. Mouse models of human KCNQ2 and KCNQ3 mutations for benign familial neonatal convulsions show seizures and neuronal plasticity without synaptic reorganization.
    Singh NA, Otto JF, Dahle EJ, Pappas C, Leslie JD, Vilaythong A, Noebels JL, White HS, Wilcox KS, Leppert MF.
    J Physiol; 2008 Jul 15; 586(14):3405-23. PubMed ID: 18483067
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