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Linkage and mutational analysis of CLCN2 in childhood absence epilepsy.
Everett K, Chioza B, Aicardi J, Aschauer H, Brouwer O, Callenbach P, Covanis A, Dooley J, Dulac O, Durner M, Eeg-Olofsson O, Feucht M, Friis M, Guerrini R, Heils A, Kjeldsen M, Nabbout R, Sander T, Wirrell E, McKeigue P, Robinson R, Taske N, Gardiner M. Everett K, et al. Epilepsy Res. 2007 Jul;75(2-3):145-53. doi: 10.1016/j.eplepsyres.2007.05.004. Epub 2007 Jun 18. Epilepsy Res. 2007. PMID: 17580110 Free article.
Genome wide high density SNP-based linkage analysis of childhood absence epilepsy identifies a susceptibility locus on chromosome 3p23-p14.
Chioza BA, Aicardi J, Aschauer H, Brouwer O, Callenbach P, Covanis A, Dooley JM, Dulac O, Durner M, Eeg-Olofsson O, Feucht M, Friis ML, Guerrini R, Kjeldsen MJ, Nabbout R, Nashef L, Sander T, Sirén A, Wirrell E, McKeigue P, Robinson R, Gardiner RM, Everett KV. Chioza BA, et al. Epilepsy Res. 2009 Dec;87(2-3):247-55. doi: 10.1016/j.eplepsyres.2009.09.010. Epub 2009 Oct 17. Epilepsy Res. 2009. PMID: 19837565 Free PMC article.
Stiripentol in Dravet syndrome: results of a retrospective U.S. study.
Wirrell EC, Laux L, Franz DN, Sullivan J, Saneto RP, Morse RP, Devinsky O, Chugani H, Hernandez A, Hamiwka L, Mikati MA, Valencia I, Le Guern ME, Chancharme L, de Menezes MS. Wirrell EC, et al. Epilepsia. 2013 Sep;54(9):1595-604. doi: 10.1111/epi.12303. Epub 2013 Jul 12. Epilepsia. 2013. PMID: 23848835 Free article.
Sleep abnormalities in children with Dravet syndrome.
Dhamija R, Erickson MK, St Louis EK, Wirrell E, Kotagal S. Dhamija R, et al. Pediatr Neurol. 2014 May;50(5):474-8. doi: 10.1016/j.pediatrneurol.2014.01.017. Epub 2014 Jan 7. Pediatr Neurol. 2014. PMID: 24656210
Pharmacotherapy for Dravet Syndrome.
Wallace A, Wirrell E, Kenney-Jung DL. Wallace A, et al. Paediatr Drugs. 2016 Jun;18(3):197-208. doi: 10.1007/s40272-016-0171-7. Paediatr Drugs. 2016. PMID: 26966048 Review.
273 results