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Journal Abstract Search

262 related items for PubMed ID: 24375629

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  • 25. Dominant-negative effects of KCNQ2 mutations are associated with epileptic encephalopathy.
    Orhan G, Bock M, Schepers D, Ilina EI, Reichel SN, Löffler H, Jezutkovic N, Weckhuysen S, Mandelstam S, Suls A, Danker T, Guenther E, Scheffer IE, De Jonghe P, Lerche H, Maljevic S.
    Ann Neurol; 2014 Mar; 75(3):382-94. PubMed ID: 24318194
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  • 26. Moderate loss of function of cyclic-AMP-modulated KCNQ2/KCNQ3 K+ channels causes epilepsy.
    Schroeder BC, Kubisch C, Stein V, Jentsch TJ.
    Nature; 1998 Dec 17; 396(6712):687-90. PubMed ID: 9872318
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  • 27. KCNQ2 encephalopathy: emerging phenotype of a neonatal epileptic encephalopathy.
    Weckhuysen S, Mandelstam S, Suls A, Audenaert D, Deconinck T, Claes LR, Deprez L, Smets K, Hristova D, Yordanova I, Jordanova A, Ceulemans B, Jansen A, Hasaerts D, Roelens F, Lagae L, Yendle S, Stanley T, Heron SE, Mulley JC, Berkovic SF, Scheffer IE, de Jonghe P.
    Ann Neurol; 2012 Jan 17; 71(1):15-25. PubMed ID: 22275249
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  • 29. 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 09; 98(21):12272-7. PubMed ID: 11572947
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  • 33. KCNQ2 mutations cause unique neonatal behavior arrests without motor seizures: Functional characterization.
    Wong SH, Liou YM, Yang JJ, Lee IC.
    Epilepsy Behav; 2024 Jul 09; 156():109798. PubMed ID: 38788659
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  • 34. [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 09; 44(7):487-91. PubMed ID: 17044971
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  • 35. Benign familial infantile epilepsy associated with KCNQ3 mutation: a rare occurrence or an underestimated event?
    Nardello R, Mangano GD, Miceli F, Fontana A, Piro E, Salpietro V.
    Epileptic Disord; 2020 Dec 01; 22(6):807-810. PubMed ID: 33337327
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  • 37. Heteromeric Assembly of Truncated Neuronal Kv7 Channels: Implications for Neurologic Disease and Pharmacotherapy.
    Li J, Maghera J, Lamothe SM, Marco EJ, Kurata HT.
    Mol Pharmacol; 2020 Sep 01; 98(3):192-202. PubMed ID: 32580997
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  • 40. 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 01; 79(1):1-5. PubMed ID: 18249525
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