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Year Number of Results
2008 2
2009 3
2010 1
2022 0
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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: abert b. 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
Palinopsia.
Abert B, Ilsen PF. Abert B, et al. Optometry. 2010 Aug;81(8):394-404. doi: 10.1016/j.optm.2009.12.010. Optometry. 2010. PMID: 20655497
[Prevalence of pervasive developmental disorders. A review].
Lenoir P, Bodier C, Desombre H, Malvy J, Abert B, Ould Taleb M, Sauvage D. Lenoir P, et al. Among authors: abert b. Encephale. 2009 Feb;35(1):36-42. doi: 10.1016/j.encep.2007.12.011. Epub 2008 Sep 23. Encephale. 2009. PMID: 19250992 Review. French.