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Comment
. 2008 Mar-Apr;8(2):37-8.
doi: 10.1111/j.1535-7511.2008.00229.x.

Channeling into the epilepsies

Comment

Channeling into the epilepsies

Tracey D Graves et al. Epilepsy Curr. 2008 Mar-Apr.
No abstract available

PubMed Disclaimer

Comment on

  • The spectrum of SCN1A-related infantile epileptic encephalopathies.
    Harkin LA, McMahon JM, Iona X, Dibbens L, Pelekanos JT, Zuberi SM, Sadleir LG, Andermann E, Gill D, Farrell K, Connolly M, Stanley T, Harbord M, Andermann F, Wang J, Batish SD, Jones JG, Seltzer WK, Gardner A; Infantile Epileptic Encephalopathy Referral Consortium; Sutherland G, Berkovic SF, Mulley JC, Scheffer IE. Harkin LA, et al. Brain. 2007 Mar;130(Pt 3):843-52. doi: 10.1093/brain/awm002. Brain. 2007. PMID: 17347258

References

    1. Scheffer IE, Berkovic SF. Generalised epilepsy with febrile seizures plus. A genetic disorder with heterogenous clinical phenotypes. Bruin. 1997;120:479–490. - PubMed
    1. Claes L, Del-Favero J, Ceulemans B, Lagae L, Van Broeckhoven C, De Jonghe P. De novo mutations in the sodium-channel gene SCNlA cause severe myoclonic epilepsy of infancy. Am J fIum Genet. 2001;68:1327–1332. - PMC - PubMed
    1. Wallace R, Hodgson BL, Grinton BE, Gardiner RM, Robinson R, Rodriguez-Casero V, Sadleir L, Morgan J, Harltin LA, Dibbens LM, Yamamoto T, Andermann E, Mulley JC, Berkovic SF, Scheffer IE. Sodium channel alpha1 -subunit mutations in severe myoclonic epilepsy of infancy and infantile spasms. Neurology. 2003;61:765–769. - PubMed
    1. Berkovic SF, Harkin I, McMahon JM, Peleltanos JT, Zuberi SM, Wirrell EC, Gill DS, Iona X, Mulley JC, Scheffer E. De-novo mutations of the sodium channel gene SCNlA in alleged vaccine encephalopathy: a retrospective study. Lancet Neurol. 2006;5:488–492. - PubMed
    1. Rhodes TI, Vanoye CG, Ohrnori I, Ogiwara 1, Yamakawa K, George AL., Jr Sodium channel dysfunction in intractable childhood epilepsy with generalized tonic-clonic seizures. JPhysiol. 2005;569(Pt 2):433–445. - PMC - PubMed