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Journal Abstract Search

809 related items for PubMed ID: 16210358

  • 1. Sodium channel dysfunction in intractable childhood epilepsy with generalized tonic-clonic seizures.
    Rhodes TH, Vanoye CG, Ohmori I, Ogiwara I, Yamakawa K, George AL.
    J Physiol; 2005 Dec 01; 569(Pt 2):433-45. PubMed ID: 16210358
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  • 3. Epilepsy-associated dysfunction in the voltage-gated neuronal sodium channel SCN1A.
    Lossin C, Rhodes TH, Desai RR, Vanoye CG, Wang D, Carniciu S, Devinsky O, George AL.
    J Neurosci; 2003 Dec 10; 23(36):11289-95. PubMed ID: 14672992
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  • 8. The voltage-gated sodium channel Scn8a is a genetic modifier of severe myoclonic epilepsy of infancy.
    Martin MS, Tang B, Papale LA, Yu FH, Catterall WA, Escayg A.
    Hum Mol Genet; 2007 Dec 01; 16(23):2892-9. PubMed ID: 17881658
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  • 9. Effect of localization of missense mutations in SCN1A on epilepsy phenotype severity.
    Kanai K, Hirose S, Oguni H, Fukuma G, Shirasaka Y, Miyajima T, Wada K, Iwasa H, Yasumoto S, Matsuo M, Ito M, Mitsudome A, Kaneko S.
    Neurology; 2004 Jul 27; 63(2):329-34. PubMed ID: 15277629
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  • 12. Nav 1.1 dysfunction in genetic epilepsy with febrile seizures-plus or Dravet syndrome.
    Volkers L, Kahlig KM, Verbeek NE, Das JH, van Kempen MJ, Stroink H, Augustijn P, van Nieuwenhuizen O, Lindhout D, George AL, Koeleman BP, Rook MB.
    Eur J Neurosci; 2011 Oct 27; 34(8):1268-75. PubMed ID: 21864321
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  • 16. Cryptogenic epileptic syndromes related to SCN1A: twelve novel mutations identified.
    Zucca C, Redaelli F, Epifanio R, Zanotta N, Romeo A, Lodi M, Veggiotti P, Airoldi G, Panzeri C, Romaniello R, De Polo G, Bonanni P, Cardinali S, Baschirotto C, Martorell L, Borgatti R, Bresolin N, Bassi MT.
    Arch Neurol; 2008 Apr 27; 65(4):489-94. PubMed ID: 18413471
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  • 17. Na channel gene mutations in epilepsy--the functional consequences.
    Yamakawa K.
    Epilepsy Res; 2006 Aug 27; 70 Suppl 1():S218-22. PubMed ID: 16806834
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  • 18. Nav1.1 channels with mutations of severe myoclonic epilepsy in infancy display attenuated currents.
    Sugawara T, Tsurubuchi Y, Fujiwara T, Mazaki-Miyazaki E, Nagata K, Montal M, Inoue Y, Yamakawa K.
    Epilepsy Res; 2003 May 27; 54(2-3):201-7. PubMed ID: 12837571
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