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Genome sequencing identifies rare tandem repeat expansions and copy number variants in Lennox-Gastaut syndrome.
Qaiser F, Sadoway T, Yin Y, Zulfiqar Ali Q, Nguyen CM, Shum N, Backstrom I, Marques PT, Tabarestani S, Munhoz RP, Krings T, Pearson CE, Yuen RKC, Andrade DM. Qaiser F, et al. Among authors: andrade dm. Brain Commun. 2021 Sep 14;3(3):fcab207. doi: 10.1093/braincomms/fcab207. eCollection 2021. Brain Commun. 2021. PMID: 34622207 Free PMC article.
Hemimegalencephaly: what happens when children get older?
Wu N, Borlot F, Ali A, Krings T, Andrade DM. Wu N, et al. Among authors: andrade dm. Dev Med Child Neurol. 2014 Sep;56(9):905-9. doi: 10.1111/dmcn.12390. Epub 2014 Feb 5. Dev Med Child Neurol. 2014. PMID: 24494819 Free article.
Aicardi syndrome: when to suspect the unexpected.
Nascimento FA, Aljaafari D, Rahim M, Krings T, Andrade D. Nascimento FA, et al. Epileptic Disord. 2016 Jun 1;18(2):216. doi: 10.1684/epd.2016.0826. Epileptic Disord. 2016. PMID: 27193831 No abstract available.
Movement disorders phenomenology in focal motor seizures.
Fasano A, Di Bonaventura C, Bove F, Espay AJ, Morgante F, Fabbrini G, Munhoz RP, Andrade D, Borlot F, Bui E, Di Gennaro G, Iorio R, Katzberg H, Luigetti M, Striano P, Defazio G, Berardelli A. Fasano A, et al. Parkinsonism Relat Disord. 2019 Apr;61:161-165. doi: 10.1016/j.parkreldis.2018.10.021. Epub 2018 Oct 16. Parkinsonism Relat Disord. 2019. PMID: 30361137
Polygenic burden in focal and generalized epilepsies.
Leu C, Stevelink R, Smith AW, Goleva SB, Kanai M, Ferguson L, Campbell C, Kamatani Y, Okada Y, Sisodiya SM, Cavalleri GL, Koeleman BPC, Lerche H, Jehi L, Davis LK, Najm IM, Palotie A, Daly MJ, Busch RM; Epi25 Consortium; Lal D. Leu C, et al. Brain. 2019 Nov 1;142(11):3473-3481. doi: 10.1093/brain/awz292. Brain. 2019. PMID: 31608925 Free PMC article.
184 results