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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1970 1
1975 2
1977 3
1978 3
1979 2
1980 2
1981 7
1982 7
1983 11
1984 6
1985 5
1986 7
1987 6
1988 9
1989 12
1990 8
1991 8
1992 6
1993 16
1994 11
1995 7
1996 12
1997 10
1998 7
1999 11
2000 12
2001 12
2002 14
2003 10
2004 6
2005 9
2006 17
2007 13
2008 18
2009 12
2010 15
2011 12
2012 9
2013 17
2014 9
2015 8
2016 8
2017 5
2018 6
2019 5
2020 3
2021 0
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Article attribute
Article type
Publication date

Search Results

380 results
Results by year
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Page 1
From genotype to phenotype in Dravet disease.
Gataullina S, Dulac O. Gataullina S, et al. Among authors: dulac o. Seizure. 2017 Jan;44:58-64. doi: 10.1016/j.seizure.2016.10.014. Epub 2016 Oct 21. Seizure. 2017. PMID: 27817982 Free article. Review.
Gene mutations in paediatric epilepsies cause NMDA-pathy, and phasic and tonic GABA-pathy.
Gataullina S, Bienvenu T, Nabbout R, Huberfeld G, Dulac O. Gataullina S, et al. Among authors: dulac o. Dev Med Child Neurol. 2019 Aug;61(8):891-898. doi: 10.1111/dmcn.14152. Epub 2019 Jan 25. Dev Med Child Neurol. 2019. PMID: 30680721 Free article. Review.
Outcome of childhood-onset epilepsy from adolescence to adulthood: Transition issues.
Nabbout R, Andrade DM, Bahi-Buisson N, Cross H, Desquerre I, Dulac O, Granata T, Hirsch E, Navarro V, Ouss L, Pearl PL, Schmidt D, Thiele E, Camfield PR, Camfield CS. Nabbout R, et al. Among authors: dulac o. Epilepsy Behav. 2017 Apr;69:161-169. doi: 10.1016/j.yebeh.2016.11.010. Epub 2017 Feb 28. Epilepsy Behav. 2017. PMID: 28256379 Review.
De novo gain-of-function KCNT1 channel mutations cause malignant migrating partial seizures of infancy.
Barcia G, Fleming MR, Deligniere A, Gazula VR, Brown MR, Langouet M, Chen H, Kronengold J, Abhyankar A, Cilio R, Nitschke P, Kaminska A, Boddaert N, Casanova JL, Desguerre I, Munnich A, Dulac O, Kaczmarek LK, Colleaux L, Nabbout R. Barcia G, et al. Among authors: dulac o. Nat Genet. 2012 Nov;44(11):1255-9. doi: 10.1038/ng.2441. Epub 2012 Oct 21. Nat Genet. 2012. PMID: 23086397 Free PMC article.
Pathogenesis, diagnosis and treatment of Rasmussen encephalitis: a European consensus statement.
Bien CG, Granata T, Antozzi C, Cross JH, Dulac O, Kurthen M, Lassmann H, Mantegazza R, Villemure JG, Spreafico R, Elger CE. Bien CG, et al. Among authors: dulac o. Brain. 2005 Mar;128(Pt 3):454-71. doi: 10.1093/brain/awh415. Epub 2005 Feb 2. Brain. 2005. PMID: 15689357 Review.
Status epilepticus.
Dulac O, Takahashi T. Dulac O, et al. Handb Clin Neurol. 2013;111:681-9. doi: 10.1016/B978-0-444-52891-9.00070-1. Handb Clin Neurol. 2013. PMID: 23622215 Review.
Are Epileptic Spasms a Seizure Type for the Insular Region?
Kharytonov V, Dulac O. Kharytonov V, et al. Among authors: dulac o. Neuropediatrics. 2020 Aug;51(4):295-297. doi: 10.1055/s-0040-1702226. Epub 2020 Mar 28. Neuropediatrics. 2020. PMID: 32221960
Epileptic encephalopathy.
Dulac O. Dulac O. Epilepsia. 2001;42 Suppl 3:23-6. doi: 10.1046/j.1528-1157.2001.042suppl.3023.x. Epilepsia. 2001. PMID: 11520318 Free article. Review.
Pediatric neurology.
Dulac O, Lassonde M, Sarnat HB. Dulac O, et al. Handb Clin Neurol. 2013;111:ix. doi: 10.1016/B978-0-444-52891-9.09995-4. Handb Clin Neurol. 2013. PMID: 23622230 No abstract available.
Basal ganglia dysmorphism in patients with Aicardi syndrome.
Masnada S, Pichiecchio A, Formica M, Arrigoni F, Borrelli P, Accorsi P, Bonanni P, Borgatti R, Bernardina BD, Danieli A, Darra F, Deconinck N, De Giorgis V, Dulac O, Gataullina S, Giordano L, Guerrini R, La Briola F, Mastrangelo M, Montomoli M, Mortilla M, Osanni E, Parisi P, Perucca E, Pinelli L, Romaniello R, Severino M, Vigevano F, Vignoli A, Bahi-Buisson N, Cavallin M, Accogli A, Burgeois M, Capra V, Chaves-Vischer V, Chiapparini L, Colafati G, D'Arrigo S, Desguerre I, Doco-Fenzy M, d'Orsi G, Epitashvili N, Fazzi E, Ferretti A, Fiorini E, Fradin M, Fusco C, Granata T, Johannesen KM, Lebon S, Loget P, Moller RS, Montanaro D, Orcesi S, Quelin C, Rebessi E, Romeo A, Solazzi R, Spagnoli C, Uebler C, Zara F, Arzimanoglou A, Veggiotti P; Aicardi Syndrome International Study Group. Masnada S, et al. Among authors: dulac o. Neurology. 2020 Dec 4:10.1212/WNL.0000000000011237. doi: 10.1212/WNL.0000000000011237. Online ahead of print. Neurology. 2020. PMID: 33277420
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