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

Year Number of Results
1996 1
1997 1
1998 3
1999 1
2001 2
2002 1
2003 1
2004 3
2005 1
2006 3
2007 5
2008 3
2009 3
2010 5
2011 4
2012 1
2013 3
2014 1
2015 3
2017 1
2018 1
2020 1
2021 2
2022 1
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47 results
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Page 1
Spectrum of SCN1A gene mutations associated with Dravet syndrome: analysis of 333 patients.
Depienne C, Trouillard O, Saint-Martin C, Gourfinkel-An I, Bouteiller D, Carpentier W, Keren B, Abert B, Gautier A, Baulac S, Arzimanoglou A, Cazeneuve C, Nabbout R, LeGuern E. Depienne C, et al. Among authors: gourfinkel an i. J Med Genet. 2009 Mar;46(3):183-91. doi: 10.1136/jmg.2008.062323. Epub 2008 Oct 17. J Med Genet. 2009. PMID: 18930999
Monogenic idiopathic epilepsies.
Gourfinkel-An I, Baulac S, Nabbout R, Ruberg M, Baulac M, Brice A, LeGuern E. Gourfinkel-An I, et al. Lancet Neurol. 2004 Apr;3(4):209-18. doi: 10.1016/S1474-4422(04)00706-9. Lancet Neurol. 2004. PMID: 15039033 Review.
SCN1A-related epilepsy with recessive inheritance: Two further families.
Moretti R, Arnaud L, Bouteiller D, Trouillard O, Moreau P, Buratti J, Rastetter A, Keren B, Des Portes V, Toulouse J, Gourfinkel-An I, Leguern E, Depienne C, Mignot C, Nava C. Moretti R, et al. Among authors: gourfinkel an i. Eur J Paediatr Neurol. 2021 Jul;33:121-124. doi: 10.1016/j.ejpn.2021.05.018. Epub 2021 Jun 5. Eur J Paediatr Neurol. 2021. PMID: 34174751
Outcome of pediatric epilepsies in adulthood.
Gourfinkel-An I, Dubeau F. Gourfinkel-An I, et al. Handb Clin Neurol. 2013;111:809-18. doi: 10.1016/B978-0-444-52891-9.00084-1. Handb Clin Neurol. 2013. PMID: 23622229 Review.
Fever, genes, and epilepsy.
Baulac S, Gourfinkel-An I, Nabbout R, Huberfeld G, Serratosa J, Leguern E, Baulac M. Baulac S, et al. Among authors: gourfinkel an i. Lancet Neurol. 2004 Jul;3(7):421-30. doi: 10.1016/S1474-4422(04)00808-7. Lancet Neurol. 2004. PMID: 15207799 Review.
Genes in infantile epileptic encephalopathies.
Depienne C, Gourfinkel-An I, Baulac S, LeGuern E. Depienne C, et al. Among authors: gourfinkel an i. In: Noebels JL, Avoli M, Rogawski MA, Olsen RW, Delgado-Escueta AV, editors. Jasper's Basic Mechanisms of the Epilepsies [Internet]. 4th edition. Bethesda (MD): National Center for Biotechnology Information (US); 2012. In: Noebels JL, Avoli M, Rogawski MA, Olsen RW, Delgado-Escueta AV, editors. Jasper's Basic Mechanisms of the Epilepsies [Internet]. 4th edition. Bethesda (MD): National Center for Biotechnology Information (US); 2012. PMID: 22787626 Free Books & Documents. Review.
Epilepsy and inborn errors of metabolism in adults: a diagnostic approach.
Sedel F, Gourfinkel-An I, Lyon-Caen O, Baulac M, Saudubray JM, Navarro V. Sedel F, et al. Among authors: gourfinkel an i. J Inherit Metab Dis. 2007 Nov;30(6):846-54. doi: 10.1007/s10545-007-0723-7. Epub 2007 Oct 22. J Inherit Metab Dis. 2007. PMID: 17957491 Review.
A clinical and neurophysiological motor signature of Unverricht-Lundborg disease.
Hainque E, Blancher A, Mesnage V, Rivaud-Pechoux S, Bertrand A, Dupont S, Navarro V, Roze E, Gourfinkel-An I, Apartis E. Hainque E, et al. Among authors: gourfinkel an i. Rev Neurol (Paris). 2018 Jan-Feb;174(1-2):56-65. doi: 10.1016/j.neurol.2017.06.005. Epub 2017 Jul 5. Rev Neurol (Paris). 2018. PMID: 28688606
47 results