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Exome Sequencing Fails to Identify the Genetic Cause of Aicardi Syndrome.
Lund C, Striano P, Sorte HS, Parisi P, Iacomino M, Sheng Y, Vigeland MD, Øye AM, Møller RS, Selmer KK, Zara F. Lund C, et al. Mol Syndromol. 2016 Sep;7(4):234-238. doi: 10.1159/000448367. Epub 2016 Aug 17. Mol Syndromol. 2016. PMID: 27781033 Free PMC article.
[Dravet syndrome as a cause of epilepsy and learning disability].
Lund C, Bremer A, Lossius MI, Selmer KK, Brodtkorb E, Nakken KO. Lund C, et al. Tidsskr Nor Laegeforen. 2012 Jan 10;132(1):44-7. doi: 10.4045/tidsskr.11.0539. Tidsskr Nor Laegeforen. 2012. PMID: 22240828 Free article. Review. Norwegian.
CHD2 mutations in Lennox-Gastaut syndrome.
Lund C, Brodtkorb E, Øye AM, Røsby O, Selmer KK. Lund C, et al. Epilepsy Behav. 2014 Apr;33:18-21. doi: 10.1016/j.yebeh.2014.02.005. Epub 2014 Mar 12. Epilepsy Behav. 2014. PMID: 24614520
Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implications.
Johannesen KM, Liu Y, Koko M, Gjerulfsen CE, Sonnenberg L, Schubert J, Fenger CD, Eltokhi A, Rannap M, Koch NA, Lauxmann S, Krüger J, Kegele J, Canafoglia L, Franceschetti S, Mayer T, Rebstock J, Zacher P, Ruf S, Alber M, Sterbova K, Lassuthová P, Vlckova M, Lemke JR, Platzer K, Krey I, Heine C, Wieczorek D, Kroell-Seger J, Lund C, Klein KM, Au PYB, Rho JM, Ho AW, Masnada S, Veggiotti P, Giordano L, Accorsi P, Hoei-Hansen CE, Striano P, Zara F, Verhelst H, Verhoeven JS, Braakman HMH, van der Zwaag B, Harder AVE, Brilstra E, Pendziwiat M, Lebon S, Vaccarezza M, Le NM, Christensen J, Grønborg S, Scherer SW, Howe J, Fazeli W, Howell KB, Leventer R, Stutterd C, Walsh S, Gerard M, Gerard B, Matricardi S, Bonardi CM, Sartori S, Berger A, Hoffman-Zacharska D, Mastrangelo M, Darra F, Vøllo A, Motazacker MM, Lakeman P, Nizon M, Betzler C, Altuzarra C, Caume R, Roubertie A, Gélisse P, Marini C, Guerrini R, Bilan F, Tibussek D, Koch-Hogrebe M, Perry MS, Ichikawa S, Dadali E, Sharkov A, Mishina I, Abramov M, Kanivets I, Korostelev S, Kutsev S, Wain KE, Eisenhauer N, Wagner M, Savatt JM, Müller-Schlüter K, Bassan H, Borovikov A, Nassogne MC, Destrée A, Schoonjans AS, Meuwissen M, Buzatu… See abstract for full author list ➔ Johannesen KM, et al. Among authors: lund c. Brain. 2022 Sep 14;145(9):2991-3009. doi: 10.1093/brain/awab321. Brain. 2022. PMID: 34431999 Free PMC article.
[Lennox-Gastaut syndrome--course and treatment].
Lund C, Brodtkorb E, Nakken KO. Lund C, et al. Tidsskr Nor Laegeforen. 2011 Jan 7;131(1):24-7. doi: 10.4045/tidsskr.09.1540. Tidsskr Nor Laegeforen. 2011. PMID: 21233883 Free article. Review. Norwegian.
Seizures that are not epileptic.
Lund C, Karterud HN. Lund C, et al. Tidsskr Nor Laegeforen. 2013 Mar 5;133(5):537. doi: 10.4045/tidsskr.13.0010. Tidsskr Nor Laegeforen. 2013. PMID: 23463068 Free article. English, Norwegian. No abstract available.
856 results