Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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

Text availability

Article attribute

Article type

Publication date

Search Results

155 results

Results by year

Filters applied: . Clear all
Page 1
Defining the Genetic Landscape of Congenital Mirror Movements in 80 Affected Individuals.
Collins Hutchinson ML, St-Onge J, Schlienger S, Boudrahem-Addour N, Mougharbel L, Michaud JF, Lloyd C, Bruneau E, Roux C, Sahly AN, Osterman B, Myers KA, Rouleau GA, Jimenez Cruz DA, Rivière JB, Accogli A, Charron F, Srour M. Collins Hutchinson ML, et al. Among authors: myers ka. Mov Disord. 2024 Feb;39(2):400-410. doi: 10.1002/mds.29669. Epub 2024 Feb 5. Mov Disord. 2024. PMID: 38314870
Epilepsy in Legius syndrome: Coincidence or causation?
Medina Lemus A, Boelman C, Myers KA. Medina Lemus A, et al. Among authors: myers ka. Am J Med Genet A. 2024 Jun;194(6):e63547. doi: 10.1002/ajmg.a.63547. Epub 2024 Jan 24. Am J Med Genet A. 2024. PMID: 38268057
mTOR Pathway Somatic Pathogenic Variants in Focal Malformations of Cortical Development: Novel Variants, Topographic Mapping, and Clinical Outcomes.
Krochmalnek E, Accogli A, St-Onge J, Addour-Boudrahem N, Prakash G, Kim SH, Brunette-Clement T, Alhajaj G, Mougharbel L, Bruneau E, Myers KA, Dubeau F, Karamchandani J, Farmer JP, Atkinson J, Hall J, Chantal Poulin C, Rosenblatt B, Lafond-Lapalme J, Weil A, Fallet-Bianco C, Albrecht S, Sonenberg N, Riviere JB, Dudley RW, Srour M. Krochmalnek E, et al. Among authors: myers ka. Neurol Genet. 2023 Oct 26;9(6):e200103. doi: 10.1212/NXG.0000000000200103. eCollection 2023 Dec. Neurol Genet. 2023. PMID: 37900581 Free PMC article.
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.
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.
155 results