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Page 1
Multimodal mapping of regional brain vulnerability to focal cortical dysplasia.
Lee HM, Hong SJ, Gill R, Caldairou B, Wang I, Zhang JG, Deleo F, Schrader D, Bartolomei F, Guye M, Cho KH, Barba C, Sisodiya S, Jackson G, Hogan RE, Wong-Kisiel L, Cascino GD, Schulze-Bonhage A, Lopes-Cendes I, Cendes F, Guerrini R, Bernhardt B, Bernasconi N, Bernasconi A. Lee HM, et al. Brain. 2023 Aug 1;146(8):3404-3415. doi: 10.1093/brain/awad060. Brain. 2023. PMID: 36852571 Free PMC article.
Long-term outcomes after nonlesional extratemporal lobe epilepsy surgery.
Noe K, Sulc V, Wong-Kisiel L, Wirrell E, Van Gompel JJ, Wetjen N, Britton J, So E, Cascino GD, Marsh WR, Meyer F, Horinek D, Giannini C, Watson R, Brinkmann BH, Stead M, Worrell GA. Noe K, et al. JAMA Neurol. 2013 Aug;70(8):1003-8. doi: 10.1001/jamaneurol.2013.209. JAMA Neurol. 2013. PMID: 23732844 Free PMC article. Review.
Statistical SPECT processing in MRI-negative epilepsy surgery.
Sulc V, Stykel S, Hanson DP, Brinkmann BH, Jones DT, Holmes DR 3rd, Robb RA, Senjem ML, Mullan BP, Watson RE Jr, Horinek D, Cascino GD, Wong-Kisiel LC, Britton JW, So EL, Worrell GA. Sulc V, et al. Neurology. 2014 Mar 18;82(11):932-9. doi: 10.1212/WNL.0000000000000209. Epub 2014 Feb 14. Neurology. 2014. PMID: 24532274 Free PMC article.
Routine vs extended outpatient EEG for the detection of interictal epileptiform discharges.
Burkholder DB, Britton JW, Rajasekaran V, Fabris RR, Cherian PJ, Kelly-Williams KM, So EL, Nickels KC, Wong-Kisiel LC, Lagerlund TD, Cascino GD, Worrell GA, Wirrell EC. Burkholder DB, et al. Neurology. 2016 Apr 19;86(16):1524-30. doi: 10.1212/WNL.0000000000002592. Epub 2016 Mar 16. Neurology. 2016. PMID: 26984946 Free PMC article.
Jeavons Syndrome: Clinical Features and Response to Treatment.
Smith KM, Youssef PE, Wirrell EC, Nickels KC, Payne ET, Britton JW, Shin C, Cascino GD, Patterson MC, Wong-Kisiel LC. Smith KM, et al. Pediatr Neurol. 2018 Sep;86:46-51. doi: 10.1016/j.pediatrneurol.2018.06.001. Epub 2018 Jul 10. Pediatr Neurol. 2018. PMID: 30082241
Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders.
Wolff M, Johannesen KM, Hedrich UBS, Masnada S, Rubboli G, Gardella E, Lesca G, Ville D, Milh M, Villard L, Afenjar A, Chantot-Bastaraud S, Mignot C, Lardennois C, Nava C, Schwarz N, Gérard M, Perrin L, Doummar D, Auvin S, Miranda MJ, Hempel M, Brilstra E, Knoers N, Verbeek N, van Kempen M, Braun KP, Mancini G, Biskup S, Hörtnagel K, Döcker M, Bast T, Loddenkemper T, Wong-Kisiel L, Baumeister FM, Fazeli W, Striano P, Dilena R, Fontana E, Zara F, Kurlemann G, Klepper J, Thoene JG, Arndt DH, Deconinck N, Schmitt-Mechelke T, Maier O, Muhle H, Wical B, Finetti C, Brückner R, Pietz J, Golla G, Jillella D, Linnet KM, Charles P, Moog U, Õiglane-Shlik E, Mantovani JF, Park K, Deprez M, Lederer D, Mary S, Scalais E, Selim L, Van Coster R, Lagae L, Nikanorova M, Hjalgrim H, Korenke GC, Trivisano M, Specchio N, Ceulemans B, Dorn T, Helbig KL, Hardies K, Stamberger H, de Jonghe P, Weckhuysen S, Lemke JR, Krägeloh-Mann I, Helbig I, Kluger G, Lerche H, Møller RS. Wolff M, et al. Brain. 2017 May 1;140(5):1316-1336. doi: 10.1093/brain/awx054. Brain. 2017. PMID: 28379373
78 results