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

Year Number of Results
2001 1
2002 3
2003 2
2005 2
2006 2
2007 3
2008 2
2009 5
2010 5
2011 4
2012 7
2013 8
2014 12
2015 9
2016 10
2017 9
2018 5
2019 9
2020 7
2021 5
2022 6
2023 3
2024 0

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97 results

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Page 1
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. Among authors: ishii a. 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.
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.
SCN8A encephalopathy: Research progress and prospects.
Meisler MH, Helman G, Hammer MF, Fureman BE, Gaillard WD, Goldin AL, Hirose S, Ishii A, Kroner BL, Lossin C, Mefford HC, Parent JM, Patel M, Schreiber J, Stewart R, Whittemore V, Wilcox K, Wagnon JL, Pearl PL, Vanderver A, Scheffer IE. Meisler MH, et al. Among authors: ishii a. Epilepsia. 2016 Jul;57(7):1027-35. doi: 10.1111/epi.13422. Epub 2016 Jun 8. Epilepsia. 2016. PMID: 27270488 Free PMC article.
HOMOLOGY FOR QUANDLES WITH PARTIAL GROUP OPERATIONS.
Carter S, Ishii A, Saito M, Tanaka K. Carter S, et al. Among authors: ishii a. Pac J Math. 2017;287(1):19-48. doi: 10.2140/pjm.2017.287.19. Epub 2017 Feb 6. Pac J Math. 2017. PMID: 33828340 Free PMC article.
Somatic mosaic deletions involving SCN1A cause Dravet syndrome.
Nakayama T, Ishii A, Yoshida T, Nasu H, Shimojima K, Yamamoto T, Kure S, Hirose S. Nakayama T, et al. Among authors: ishii a. Am J Med Genet A. 2018 Mar;176(3):657-662. doi: 10.1002/ajmg.a.38596. Epub 2018 Jan 17. Am J Med Genet A. 2018. PMID: 29341473
97 results