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

Year Number of Results
2002 3
2003 4
2004 8
2005 7
2006 14
2007 13
2008 3
2009 1
2010 7
2011 4
2012 3
2013 10
2014 6
2015 9
2016 10
2017 8
2018 3
2019 5
2020 4
2021 4
2022 1
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109 results
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Page 1
Efficacy of Istradefylline for the Treatment of ADCY5-Related Disease.
Miyamoto R, Kawarai T, Takeuchi T, Izumi Y, Goto S, Kaji R. Miyamoto R, et al. Among authors: kawarai t. Mov Disord Clin Pract. 2020 Sep 7;7(7):852-853. doi: 10.1002/mdc3.13067. eCollection 2020 Oct. Mov Disord Clin Pract. 2020. PMID: 33043083 Free PMC article.
[Dystonia genes and elucidation of their roles in dystonia pathogenesis].
Kawarai T, Miyamoto R, Murakami N, Miyazaki Y, Koizumi H, Sako W, Mukai Y, Sato K, Matsumoto S, Sakamoto T, Izumi Y, Kaji R. Kawarai T, et al. Rinsho Shinkeigaku. 2013;53(6):419-29. doi: 10.5692/clinicalneurol.53.419. Rinsho Shinkeigaku. 2013. PMID: 23782819 Review. Japanese.
Rapid-Onset Dystonia-Parkinsonism Phenotype Consistency for a Novel Variant of ATP1A3 in Patients Across 3 Global Populations.
Hoshino K, Sweadner KJ, Kawarai T, Saute JA, Freitas J, Damásio J, Donis KC, Kimura K, Fukuda H, Hayashi M, Higuchi T, Ikeda Y, Ozelius LJ, Kaji R. Hoshino K, et al. Among authors: kawarai t. Neurol Genet. 2021 Mar 15;7(2):e562. doi: 10.1212/NXG.0000000000000562. eCollection 2021 Apr. Neurol Genet. 2021. PMID: 33977143 Free PMC article. No abstract available.
Phenotype variability and allelic heterogeneity in KMT2B-Associated disease.
Kawarai T, Miyamoto R, Nakagawa E, Koichihara R, Sakamoto T, Mure H, Morigaki R, Koizumi H, Oki R, Montecchiani C, Caltagirone C, Orlacchio A, Hattori A, Mashimo H, Izumi Y, Mezaki T, Kumada S, Taniguchi M, Yokochi F, Saitoh S, Goto S, Kaji R. Kawarai T, et al. Parkinsonism Relat Disord. 2018 Jul;52:55-61. doi: 10.1016/j.parkreldis.2018.03.022. Epub 2018 Apr 5. Parkinsonism Relat Disord. 2018. PMID: 29653907
109 results