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Remarkable effect of transdermal nicotine in children with CHRNA4-related autosomal dominant sleep-related hypermotor epilepsy.
Lossius K, de Saint Martin A, Myren-Svelstad S, Bjørnvold M, Minken G, Seegmuller C, Valenti Hirsch MP, Chelly J, Steinlein O, Picard F, Brodtkorb E. Lossius K, et al. Among authors: seegmuller c. Epilepsy Behav. 2020 Apr;105:106944. doi: 10.1016/j.yebeh.2020.106944. Epub 2020 Feb 22. Epilepsy Behav. 2020. PMID: 32097883 Free article.
Idiopathic focal epilepsies: the "lost tribe".
Pal DK, Ferrie C, Addis L, Akiyama T, Capovilla G, Caraballo R, de Saint-Martin A, Fejerman N, Guerrini R, Hamandi K, Helbig I, Ioannides AA, Kobayashi K, Lal D, Lesca G, Muhle H, Neubauer BA, Pisano T, Rudolf G, Seegmuller C, Shibata T, Smith A, Striano P, Strug LJ, Szepetowski P, Valeta T, Yoshinaga H, Koutroumanidis M. Pal DK, et al. Among authors: seegmuller c. Epileptic Disord. 2016 Sep 1;18(3):252-88. doi: 10.1684/epd.2016.0839. Epileptic Disord. 2016. PMID: 27435520 Review. English.
Landau-Kleffner syndrome is not an eponymic badge of ignorance.
Hirsch E, Valenti MP, Rudolf G, Seegmuller C, de Saint Martin A, Maquet P, Wioland N, Metz-Lutz MN, Marescaux C, Arzimanoglou A. Hirsch E, et al. Among authors: seegmuller c. Epilepsy Res. 2006 Aug;70 Suppl 1:S239-47. doi: 10.1016/j.eplepsyres.2006.02.010. Epub 2006 Jun 27. Epilepsy Res. 2006. PMID: 16806832 Review.
Landau-Kleffner syndrome: sleep EEG characteristics at onset.
Massa R, de Saint-Martin A, Hirsch E, Marescaux C, Motte J, Seegmuller C, Kleitz C, Metz-Lutz M. Massa R, et al. Among authors: seegmuller c. Clin Neurophysiol. 2000 Sep;111 Suppl 2:S87-93. doi: 10.1016/s1388-2457(00)00407-7. Clin Neurophysiol. 2000. PMID: 10996560
Intelligence quotient improves after antiepileptic drug withdrawal following pediatric epilepsy surgery.
Boshuisen K, van Schooneveld MM, Uiterwaal CS, Cross JH, Harrison S, Polster T, Daehn M, Djimjadi S, Yalnizoglu D, Turanli G, Sassen R, Hoppe C, Kuczaty S, Barba C, Kahane P, Schubert-Bast S, Reuner G, Bast T, Strobl K, Mayer H, de Saint-Martin A, Seegmuller C, Laurent A, Arzimanoglou A, Braun KP; TimeToStop cognitive outcome study group. Boshuisen K, et al. Among authors: seegmuller c. Ann Neurol. 2015 Jul;78(1):104-14. doi: 10.1002/ana.24427. Ann Neurol. 2015. PMID: 25899932
SRPX2 mutations in disorders of language cortex and cognition.
Roll P, Rudolf G, Pereira S, Royer B, Scheffer IE, Massacrier A, Valenti MP, Roeckel-Trevisiol N, Jamali S, Beclin C, Seegmuller C, Metz-Lutz MN, Lemainque A, Delepine M, Caloustian C, de Saint Martin A, Bruneau N, Depétris D, Mattéi MG, Flori E, Robaglia-Schlupp A, Lévy N, Neubauer BA, Ravid R, Marescaux C, Berkovic SF, Hirsch E, Lathrop M, Cau P, Szepetowski P. Roll P, et al. Among authors: seegmuller c. Hum Mol Genet. 2006 Apr 1;15(7):1195-207. doi: 10.1093/hmg/ddl035. Epub 2006 Feb 23. Hum Mol Genet. 2006. PMID: 16497722
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