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Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancy.
Nabbout R, Gennaro E, Dalla Bernardina B, Dulac O, Madia F, Bertini E, Capovilla G, Chiron C, Cristofori G, Elia M, Fontana E, Gaggero R, Granata T, Guerrini R, Loi M, La Selva L, Lispi ML, Matricardi A, Romeo A, Tzolas V, Valseriati D, Veggiotti P, Vigevano F, Vallée L, Dagna Bricarelli F, Bianchi A, Zara F. Nabbout R, et al. Among authors: dulac o. Neurology. 2003 Jun 24;60(12):1961-7. doi: 10.1212/01.wnl.0000069463.41870.2f. Neurology. 2003. PMID: 12821740
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.
Absence of mutations in major GEFS+ genes in myoclonic astatic epilepsy.
Nabbout R, Kozlovski A, Gennaro E, Bahi-Buisson N, Zara F, Chiron C, Bianchi A, Brice A, Leguern E, Dulac O. Nabbout R, et al. Among authors: dulac o. Epilepsy Res. 2003 Oct;56(2-3):127-33. doi: 10.1016/j.eplepsyres.2003.08.007. Epilepsy Res. 2003. PMID: 14642997
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.
Motor neuropathy contributes to crouching in patients with Dravet syndrome.
Gitiaux C, Chemaly N, Quijano-Roy S, Barnerias C, Desguerre I, Hully M, Chiron C, Dulac O, Nabbout R. Gitiaux C, et al. Among authors: dulac o. Neurology. 2016 Jul 19;87(3):277-81. doi: 10.1212/WNL.0000000000002859. Epub 2016 Jun 17. Neurology. 2016. PMID: 27316242
Epileptic encephalopathies: a brief overview.
Nabbout R, Dulac O. Nabbout R, et al. Among authors: dulac o. J Clin Neurophysiol. 2003 Nov-Dec;20(6):393-7. doi: 10.1097/00004691-200311000-00002. J Clin Neurophysiol. 2003. PMID: 14734929 Review.
389 results