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Genotypic and phenotypic spectrum of pyridoxine-dependent epilepsy (ALDH7A1 deficiency).
Mills PB, Footitt EJ, Mills KA, Tuschl K, Aylett S, Varadkar S, Hemingway C, Marlow N, Rennie J, Baxter P, Dulac O, Nabbout R, Craigen WJ, Schmitt B, Feillet F, Christensen E, De Lonlay P, Pike MG, Hughes MI, Struys EA, Jakobs C, Zuberi SM, Clayton PT. Mills PB, et al. Among authors: dulac o. Brain. 2010 Jul;133(Pt 7):2148-59. doi: 10.1093/brain/awq143. Epub 2010 Jun 16. Brain. 2010. PMID: 20554659 Free PMC article.
Epileptic syndromes in infancy and childhood.
Nabbout R, Dulac O. Nabbout R, et al. Among authors: dulac o. Curr Opin Neurol. 2008 Apr;21(2):161-6. doi: 10.1097/WCO.0b013e3282f7007e. Curr Opin Neurol. 2008. PMID: 18317274 Review.
Pyridoxine dependent epilepsy: a suggestive electroclinical pattern.
Nabbout R, Soufflet C, Plouin P, Dulac O. Nabbout R, et al. Among authors: dulac o. Arch Dis Child Fetal Neonatal Ed. 1999 Sep;81(2):F125-9. doi: 10.1136/fn.81.2.f125. Arch Dis Child Fetal Neonatal Ed. 1999. PMID: 10448181 Free PMC article.
Parental view of epilepsy in Rett Syndrome.
Bahi-Buisson N, Guellec I, Nabbout R, Guet A, Nguyen G, Dulac O, Chiron C. Bahi-Buisson N, et al. Among authors: dulac o. Brain Dev. 2008 Feb;30(2):126-30. doi: 10.1016/j.braindev.2007.07.002. Epub 2007 Aug 17. Brain Dev. 2008. PMID: 17707604
Protocadherin 19 mutations in girls with infantile-onset epilepsy.
Nabbout R, Depienne C, Chiron C, Dulac O. Nabbout R, et al. Among authors: dulac o. Neurology. 2011 Mar 29;76(13):1193-4; author reply 1194. doi: 10.1212/WNL.0b013e31820a9642. Neurology. 2011. PMID: 21444909 No abstract available.
389 results