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Page 1
Do mutations in SCN1B cause Dravet syndrome?
Kim YO, Dibbens L, Marini C, Suls A, Chemaly N, Mei D, McMahon JM, Iona X, Berkovic SF, De Jonghe P, Guerrini R, Nabbout R, Scheffer IE. Kim YO, et al. Among authors: chemaly n. Epilepsy Res. 2013 Jan;103(1):97-100. doi: 10.1016/j.eplepsyres.2012.10.009. Epub 2012 Nov 20. Epilepsy Res. 2013. PMID: 23182416
[Epidemicology des epilepsies].
Chemaly N, Nabbout R. Chemaly N, et al. Rev Prat. 2012 Dec;62(10):1388-9. Rev Prat. 2012. PMID: 23424918 Review. French. No abstract available.
Arterial Spin Labeling MRI: a step forward in non-invasive delineation of focal cortical dysplasia in children.
Blauwblomme T, Boddaert N, Chémaly N, Chiron C, Pages M, Varlet P, Bourgeois M, Bahi-Buisson N, Kaminska A, Grevent D, Brunelle F, Sainte-Rose C, Archambaud F, Nabbout R. Blauwblomme T, et al. Among authors: chemaly n. Epilepsy Res. 2014 Dec;108(10):1932-9. doi: 10.1016/j.eplepsyres.2014.09.029. Epub 2014 Oct 13. Epilepsy Res. 2014. PMID: 25454505
From splitting GLUT1 deficiency syndromes to overlapping phenotypes.
Hully M, Vuillaumier-Barrot S, Le Bizec C, Boddaert N, Kaminska A, Lascelles K, de Lonlay P, Cances C, des Portes V, Roubertie A, Doummar D, LeBihannic A, Degos B, de Saint Martin A, Flori E, Pedespan JM, Goldenberg A, Vanhulle C, Bekri S, Roubergue A, Heron B, Cournelle MA, Kuster A, Chenouard A, Loiseau MN, Valayannopoulos V, Chemaly N, Gitiaux C, Seta N, Bahi-Buisson N. Hully M, et al. Among authors: chemaly n. Eur J Med Genet. 2015 Sep;58(9):443-54. doi: 10.1016/j.ejmg.2015.06.007. Epub 2015 Jul 17. Eur J Med Genet. 2015. PMID: 26193382
55 results