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Journal Abstract Search

134 related items for PubMed ID: 33337327

  • 1. 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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  • 4. 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 01; 17(3):308-10. PubMed ID: 23146207
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  • 10. Phenotypes and PRRT2 mutations in Chinese families with benign familial infantile epilepsy and infantile convulsions with paroxysmal choreoathetosis.
    Yang X, Zhang Y, Xu X, Wang S, Yang Z, Wu Y, Liu X, Wu X.
    BMC Neurol; 2013 Dec 26; 13():209. PubMed ID: 24370076
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  • 11. A novel mutation in KCNQ3-related benign familial neonatal epilepsy: electroclinical features and neurodevelopmental outcome.
    Piro E, Nardello R, Gennaro E, Fontana A, Taglialatela M, Mangano GD, Corsello G, Mangano S.
    Epileptic Disord; 2019 Feb 01; 21(1):87-91. PubMed ID: 30782577
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  • 12. 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, BFNC Physician Consortium.
    Brain; 2003 Dec 01; 126(Pt 12):2726-37. PubMed ID: 14534157
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  • 15. Lack of potassium current in W309R mutant KCNQ3 channel causing benign familial neonatal convulsions (BFNC).
    Sugiura Y, Nakatsu F, Hiroyasu K, Ishii A, Hirose S, Okada M, Jibiki I, Ohno H, Kaneko S, Ugawa Y.
    Epilepsy Res; 2009 Mar 01; 84(1):82-5. PubMed ID: 19167866
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  • 19. 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 15; 71(3):177-83. PubMed ID: 18625963
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