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Page 1
French guidelines on stereoelectroencephalography (SEEG).
Isnard J, Taussig D, Bartolomei F, Bourdillon P, Catenoix H, Chassoux F, Chipaux M, Clémenceau S, Colnat-Coulbois S, Denuelle M, Derrey S, Devaux B, Dorfmüller G, Gilard V, Guenot M, Job-Chapron AS, Landré E, Lebas A, Maillard L, McGonigal A, Minotti L, Montavont A, Navarro V, Nica A, Reyns N, Scholly J, Sol JC, Szurhaj W, Trebuchon A, Tyvaert L, Valenti-Hirsch MP, Valton L, Vignal JP, Sauleau P. Isnard J, et al. Among authors: valton l. Neurophysiol Clin. 2018 Feb;48(1):5-13. doi: 10.1016/j.neucli.2017.11.005. Epub 2017 Dec 23. Neurophysiol Clin. 2018. PMID: 29277357 Review.
CACNA1A-associated epilepsy: Electroclinical findings and treatment response on seizures in 18 patients.
Le Roux M, Barth M, Gueden S, Desbordes de Cepoy P, Aeby A, Vilain C, Hirsch E, de Saint Martin A, Portes VD, Lesca G, Riquet A, Chaton L, Villeneuve N, Villard L, Cances C, Valton L, Renaldo F, Vermersch AI, Altuzarra C, Nguyen-Morel MA, Van Gils J, Angelini C, Biraben A, Arnaud L, Riant F, Van Bogaert P. Le Roux M, et al. Among authors: valton l. Eur J Paediatr Neurol. 2021 Jul;33:75-85. doi: 10.1016/j.ejpn.2021.05.010. Epub 2021 May 26. Eur J Paediatr Neurol. 2021. PMID: 34102571 Free article.
Etiological assessment of status epilepticus.
Valton L, Benaiteau M, Denuelle M, Rulquin F, Hachon Le Camus C, Hein C, Viguier A, Curot J. Valton L, et al. Rev Neurol (Paris). 2020 Jun;176(6):408-426. doi: 10.1016/j.neurol.2019.12.010. Epub 2020 Apr 21. Rev Neurol (Paris). 2020. PMID: 32331701 Review.
Planning and management of SEEG.
Chassoux F, Navarro V, Catenoix H, Valton L, Vignal JP. Chassoux F, et al. Among authors: valton l. Neurophysiol Clin. 2018 Feb;48(1):25-37. doi: 10.1016/j.neucli.2017.11.007. Epub 2017 Dec 15. Neurophysiol Clin. 2018. PMID: 29254835 Review.
[Mood disorders and epilepsy surgery: A review].
Yrondi A, Arbus C, Valton L, Schmitt L. Yrondi A, et al. Among authors: valton l. Encephale. 2017 Apr;43(2):154-159. doi: 10.1016/j.encep.2016.02.015. Epub 2016 Jun 2. Encephale. 2017. PMID: 27265566 Review. French.
Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes.
Chen S, Abou-Khalil BW, Afawi Z, Ali QZ, Amadori E, Anderson A, Anderson J, Andrade DM, Annesi G, Arslan M, Auce P, Bahlo M, Baker MD, Balagura G, Balestrini S, Banks E, Barba C, Barboza K, Bartolomei F, Bass N, Baum LW, Baumgartner TH, Baykan B, Bebek N, Becker F, Bennett CA, Beydoun A, Bianchini C, Bisulli F, Blackwood D, Blatt I, Borggräfe I, Bosselmann C, Braatz V, Brand H, Brockmann K, Buono RJ, Busch RM, Caglayan SH, Canafoglia L, Canavati C, Castellotti B, Cavalleri GL, Cerrato F, Chassoux F, Cherian C, Cherny SS, Cheung CL, Chou IJ, Chung SK, Churchhouse C, Ciullo V, Clark PO, Cole AJ, Cosico M, Cossette P, Cotsapas C, Cusick C, Daly MJ, Davis LK, Jonghe P, Delanty N, Dennig D, Depondt C, Derambure P, Devinsky O, Di Vito L, Dickerson F, Dlugos DJ, Doccini V, Doherty CP, El-Naggar H, Ellis CA, Epstein L, Evans M, Faucon A, Feng YA, Ferguson L, Ferraro TN, Da Silva IF, Ferri L, Feucht M, Fields MC, Fitzgerald M, Fonferko-Shadrach B, Fortunato F, Franceschetti S, French JA, Freri E, Fu JM, Gabriel S, Gagliardi M, Gambardella A, Gauthier L, Giangregorio T, Gili T, Glauser TA, Goldberg E, Goldman A, Goldstein DB, Granata T, Grant R, Greenberg DA, Guerrini R, Gundogdu-Eken A, Gu… See abstract for full author list ➔ Chen S, et al. Among authors: valton l. medRxiv [Preprint]. 2024 Sep 20:2023.02.22.23286310. doi: 10.1101/2023.02.22.23286310. medRxiv. 2024. Update in: Nat Neurosci. 2024 Oct;27(10):1864-1879. doi: 10.1038/s41593-024-01747-8 PMID: 36865150 Free PMC article. Updated. Preprint.
67 results