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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1993 1
2002 3
2003 3
2004 2
2005 2
2006 4
2007 4
2008 1
2009 1
2010 4
2011 3
2012 3
2013 4
2014 6
2015 6
2016 8
2017 17
2018 18
2019 15
2020 17
2021 16
2022 19
2023 15
2024 6

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155 results

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Page 1
Genetic Epilepsy Syndromes.
Myers KA. Myers KA. Continuum (Minneap Minn). 2022 Apr 1;28(2):339-362. doi: 10.1212/CON.0000000000001077. Continuum (Minneap Minn). 2022. PMID: 35393962 Review.
The Genetic Landscape of Epilepsy of Infancy with Migrating Focal Seizures.
Burgess R, Wang S, McTague A, Boysen KE, Yang X, Zeng Q, Myers KA, Rochtus A, Trivisano M, Gill D; EIMFS Consortium; Sadleir LG, Specchio N, Guerrini R, Marini C, Zhang YH, Mefford HC, Kurian MA, Poduri AH, Scheffer IE. Burgess R, et al. Among authors: myers ka. Ann Neurol. 2019 Dec;86(6):821-831. doi: 10.1002/ana.25619. Ann Neurol. 2019. PMID: 31618474 Free PMC article.
Clinical and functional heterogeneity associated with the disruption of retinoic acid receptor beta.
Caron V, Chassaing N, Ragge N, Boschann F, Ngu AM, Meloche E, Chorfi S, Lakhani SA, Ji W, Steiner L, Marcadier J, Jansen PR, van de Pol LA, van Hagen JM, Russi AS, Le Guyader G, Nordenskjöld M, Nordgren A, Anderlid BM, Plaisancié J, Stoltenburg C, Horn D, Drenckhahn A, Hamdan FF, Lefebvre M, Attie-Bitach T, Forey P, Smirnov V, Ernould F, Jacquemont ML, Grotto S, Alcantud A, Coret A, Ferrer-Avargues R, Srivastava S, Vincent-Delorme C, Romoser S, Safina N, Saade D, Lupski JR, Calame DG, Geneviève D, Chatron N, Schluth-Bolard C, Myers KA, Dobyns WB, Calvas P; DDD Study; Salmon C, Holt R, Elmslie F, Allaire M, Prigozhin DM, Tremblay A, Michaud JL. Caron V, et al. Among authors: myers ka. Genet Med. 2023 Aug;25(8):100856. doi: 10.1016/j.gim.2023.100856. Epub 2023 Apr 20. Genet Med. 2023. PMID: 37092537 Free article.
SCN1A as a therapeutic target for Dravet syndrome.
Myers KA. Myers KA. Expert Opin Ther Targets. 2023 Jan-Jun;27(6):459-467. doi: 10.1080/14728222.2023.2230364. Epub 2023 Jun 29. Expert Opin Ther Targets. 2023. PMID: 37364240 Review.
GRIN2A-Related Speech Disorders and Epilepsy.
Myers KA, Scheffer IE. Myers KA, et al. 2016 Sep 29. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2016 Sep 29. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 27683935 Free Books & Documents. Review.
SUDEP risk and autonomic dysfunction in genetic epilepsies.
Sahly AN, Shevell M, Sadleir LG, Myers KA. Sahly AN, et al. Among authors: myers ka. Auton Neurosci. 2022 Jan;237:102907. doi: 10.1016/j.autneu.2021.102907. Epub 2021 Nov 10. Auton Neurosci. 2022. PMID: 34773737 Review.
Ataxia and Diplopia: A New SCN8A-Related Phenotype.
Laliberté A, Myers KA. Laliberté A, et al. Among authors: myers ka. Neurol Genet. 2023 Jul 10;9(4):e200085. doi: 10.1212/NXG.0000000000200085. eCollection 2023 Aug. Neurol Genet. 2023. PMID: 37440794 Free PMC article.
The phenotypic spectrum of epilepsy associated with periventricular nodular heterotopia.
Paliotti K, Dassi C, Berrahmoune S, Bejaran ML, Davila CEV, Martinez AB, Estupiñà MCF, Mancardi MM, Riva A, Giacomini T, Severino M, Romaniello R, Dubeau F, Srour M, Myers KA. Paliotti K, et al. Among authors: myers ka. J Neurol. 2023 Aug;270(8):3934-3945. doi: 10.1007/s00415-023-11724-z. Epub 2023 Apr 29. J Neurol. 2023. PMID: 37119372
DEPDC5 as a potential therapeutic target for epilepsy.
Myers KA, Scheffer IE. Myers KA, et al. Expert Opin Ther Targets. 2017 Jun;21(6):591-600. doi: 10.1080/14728222.2017.1316715. Epub 2017 Apr 13. Expert Opin Ther Targets. 2017. PMID: 28406046 Review.
155 results