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 9
2003 7
2004 7
2005 4
2006 6
2007 3
2008 11
2009 10
2010 8
2011 18
2012 21
2013 19
2014 18
2015 17
2016 15
2017 11
2018 10
2019 13
2020 9
2021 13
2022 8
2023 7
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

209 results

Results by year

Filters applied: . Clear all
Page 1
Autosomal Dominant Sleep-Related Hypermotor (Hyperkinetic) Epilepsy.
Kurahashi H, Hirose S. Kurahashi H, et al. Among authors: hirose s. 2002 May 16 [updated 2023 Mar 23]. 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. 2002 May 16 [updated 2023 Mar 23]. 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: 20301348 Free Books & Documents. Review.
Genetics and gene therapy in Dravet syndrome.
Higurashi N, Broccoli V, Hirose S. Higurashi N, et al. Among authors: hirose s. Epilepsy Behav. 2022 Jun;131(Pt B):108043. doi: 10.1016/j.yebeh.2021.108043. Epub 2021 May 28. Epilepsy Behav. 2022. PMID: 34053869 Review.
Clinical spectrum of SCN2A mutations.
Shi X, Yasumoto S, Kurahashi H, Nakagawa E, Fukasawa T, Uchiya S, Hirose S. Shi X, et al. Among authors: hirose s. Brain Dev. 2012 Aug;34(7):541-5. doi: 10.1016/j.braindev.2011.09.016. Epub 2011 Oct 24. Brain Dev. 2012. PMID: 22029951 Review.
Genetics of temporal lobe epilepsy.
Hwang SK, Hirose S. Hwang SK, et al. Among authors: hirose s. Brain Dev. 2012 Sep;34(8):609-16. doi: 10.1016/j.braindev.2011.10.008. Epub 2011 Nov 21. Brain Dev. 2012. PMID: 22105092 Review.
Application of induced pluripotent stem cells in epilepsy.
Hirose S, Tanaka Y, Shibata M, Kimura Y, Ishikawa M, Higurashi N, Yamamoto T, Ichise E, Chiyonobu T, Ishii A. Hirose S, et al. Mol Cell Neurosci. 2020 Oct;108:103535. doi: 10.1016/j.mcn.2020.103535. Epub 2020 Aug 4. Mol Cell Neurosci. 2020. PMID: 32758699 Review.
Nicotinic acetylcholine receptor mutations.
Steinlein OK, Kaneko S, Hirose S. Steinlein OK, et al. Among authors: hirose s. In: Noebels JL, Avoli M, Rogawski MA, Olsen RW, Delgado-Escueta AV, editors. Jasper's Basic Mechanisms of the Epilepsies [Internet]. 4th edition. Bethesda (MD): National Center for Biotechnology Information (US); 2012. In: Noebels JL, Avoli M, Rogawski MA, Olsen RW, Delgado-Escueta AV, editors. Jasper's Basic Mechanisms of the Epilepsies [Internet]. 4th edition. Bethesda (MD): National Center for Biotechnology Information (US); 2012. PMID: 22787678 Free Books & Documents. Review.
Distinct neurological disorders with ATP1A3 mutations.
Heinzen EL, Arzimanoglou A, Brashear A, Clapcote SJ, Gurrieri F, Goldstein DB, Jóhannesson SH, Mikati MA, Neville B, Nicole S, Ozelius LJ, Poulsen H, Schyns T, Sweadner KJ, van den Maagdenberg A, Vilsen B; ATP1A3 Working Group. Heinzen EL, et al. Lancet Neurol. 2014 May;13(5):503-14. doi: 10.1016/S1474-4422(14)70011-0. Lancet Neurol. 2014. PMID: 24739246 Free PMC article. Review.
Genetics of idiopathic epilepsies.
Hirose S, Mitsudome A, Okada M, Kaneko S; Epilepsy Genetic Study Group, Japan. Hirose S, et al. Epilepsia. 2005;46 Suppl 1:38-43. doi: 10.1111/j.0013-9580.2005.461011.x. Epilepsia. 2005. PMID: 15816978 Free article. Review.
209 results