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Genetic Testing to Inform Epilepsy Treatment Management From an International Study of Clinical Practice.
JAMA Neurol. 2022 Dec 1;79(12):1267-1276. doi: 10.1001/jamaneurol.2022.3651.
JAMA Neurol. 2022.
PMID: 36315135
Free PMC article.
Epilepsy and Electroencephalographic Abnormalities in SATB2-Associated Syndrome.
Lewis H, Samanta D, Örsell JL, Bosanko KA, Rowell A, Jones M, Dale RC, Taravath S, Hahn CD, Krishnakumar D, Chagnon S, Keller S, Hagebeuk E, Pathak S, Bebin EM, Arndt DH, Alexander JJ, Mainali G, Coppola G, Maclean J, Sparagana S, McNamara N, Smith DM, Raggio V, Cruz M, Fernández-Jaén A, Kava MP, Emrick L, Fish JL, Vanderver A, Helman G, Pierson TM, Zarate YA.
Lewis H, et al.
Pediatr Neurol. 2020 Nov;112:94-100. doi: 10.1016/j.pediatrneurol.2020.04.006. Epub 2020 Apr 13.
Pediatr Neurol. 2020.
PMID: 32446642
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Early genetic testing in pediatric epilepsy: Diagnostic and cost implications.
Swartwood SM, Morales A, Hatchell KE, Moretz C, McKnight D, Demmer L, Chagnon S, Aradhya S, Esplin ED, Bonkowsky JL.
Swartwood SM, et al.
Epilepsia Open. 2024 Feb;9(1):439-444. doi: 10.1002/epi4.12878. Epub 2023 Dec 16.
Epilepsia Open. 2024.
PMID: 38071479
Free PMC article.
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Child neurology: tick paralysis: a diagnosis not to miss.
Chagnon SL, Naik M, Abdel-Hamid H.
Chagnon SL, et al.
Neurology. 2014 Mar 18;82(11):e91-3. doi: 10.1212/WNL.0000000000000216.
Neurology. 2014.
PMID: 24638220
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Early treatment is associated with improved cognition in Hurler syndrome.
Poe MD, Chagnon SL, Escolar ML.
Poe MD, et al. Among authors: chagnon sl.
Ann Neurol. 2014 Nov;76(5):747-53. doi: 10.1002/ana.24246. Epub 2014 Oct 8.
Ann Neurol. 2014.
PMID: 25103575
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