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

Year Number of Results
2010 1
2011 1
2012 2
2013 1
2014 4
2015 6
2016 1
2017 2
2018 1
2019 2
2020 2
2021 0
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17 results
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Page 1
Hokuriku-plus familial hypercholesterolaemia registry study: rationale and study design.
Tada H, Okada H, Yoshida S, Shimojima M, Nomura A, Tsuda T, Mori M, Takashima SI, Kato T, Usui S, Sakata K, Hayashi K, Fujino N, Inazu A, Takahara S, Imai Y, Matsubara T, Nohara A, Miwa K, Namura M, Terai H, Yoshida T, Araki T, Minamoto M, Aburao T, Ito Y, Nakanishi C, Kawasaki S, Todo Y, Koizumi J, Kita Y, Matsumoto H, Shintaku H, Hodatsu A, Ino H, Higashikata T, Takata M, Misawa K, Yamaguchi M, Noji Y, Osato K, Mabuchi T, Ichise T, Kaku B, Katsuda S, Fujimoto M, Uchiyama K, Fujioka K, Nakahashi T, Nozue T, Michishita I, Usuda K, Otowa K, Okeie K, Hirota S, Aburadani I, Kurokawa K, Takatori O, Hondo S, Oda H, Takata S, Murai H, Kinoshita M, Nagai H, Sekiguchi Y, Sakagami S, Omi W, Fujita C, Katsuki T, Ootsuji H, Igarashi A, Nakano M, Okura S, Maeno K, Mitamura Y, Sugimoto N, Yamamoto M, Akao H, Kajinami K, Takamura M, Kawashiri MA. Tada H, et al. Among authors: hodatsu a. BMJ Open. 2020 Sep 10;10(9):e038623. doi: 10.1136/bmjopen-2020-038623. BMJ Open. 2020. PMID: 32912992 Free PMC article.
Impact of functional studies on exome sequence variant interpretation in early-onset cardiac conduction system diseases.
Hayashi K, Teramoto R, Nomura A, Asano Y, Beerens M, Kurata Y, Kobayashi I, Fujino N, Furusho H, Sakata K, Onoue K, Chiang DY, Kiviniemi TO, Buys E, Sips P, Burch ML, Zhao Y, Kelly AE, Namura M, Kita Y, Tsuchiya T, Kaku B, Oe K, Takeda Y, Konno T, Inoue M, Fujita T, Kato T, Funada A, Tada H, Hodatsu A, Nakanishi C, Sakamoto Y, Tsuda T, Nagata Y, Tanaka Y, Okada H, Usuda K, Cui S, Saito Y, MacRae CA, Takashima S, Yamagishi M, Kawashiri MA, Takamura M. Hayashi K, et al. Among authors: hodatsu a. Cardiovasc Res. 2020 Nov 1;116(13):2116-2130. doi: 10.1093/cvr/cvaa010. Cardiovasc Res. 2020. PMID: 31977013
J Waves for Predicting Cardiac Events in Hypertrophic Cardiomyopathy.
Tsuda T, Hayashi K, Konno T, Sakata K, Fujita T, Hodatsu A, Nagata Y, Teramoto R, Nomura A, Tanaka Y, Furusho H, Takamura M, Kawashiri MA, Fujino N, Yamagishi M. Tsuda T, et al. Among authors: hodatsu a. JACC Clin Electrophysiol. 2017 Oct;3(10):1136-1142. doi: 10.1016/j.jacep.2017.03.010. Epub 2017 Jun 28. JACC Clin Electrophysiol. 2017. PMID: 29759496 Free article.
A KCR1 variant implicated in susceptibility to the long QT syndrome.
Hayashi K, Fujino N, Ino H, Uchiyama K, Sakata K, Konno T, Masuta E, Funada A, Sakamoto Y, Tsubokawa T, Hodatsu A, Yasuda T, Kanaya H, Kim MY, Kupershmidt S, Higashida H, Yamagishi M. Hayashi K, et al. Among authors: hodatsu a. J Mol Cell Cardiol. 2011 Jan;50(1):50-7. doi: 10.1016/j.yjmcc.2010.10.007. Epub 2010 Oct 13. J Mol Cell Cardiol. 2011. PMID: 20950623
Impact of systolic dysfunction in genotyped hypertrophic cardiomyopathy.
Fujino N, Konno T, Hayashi K, Hodatsu A, Fujita T, Tsuda T, Nagata Y, Kawashiri MA, Ino H, Yamagishi M. Fujino N, et al. Among authors: hodatsu a. Clin Cardiol. 2013 Mar;36(3):160-5. doi: 10.1002/clc.22082. Epub 2012 Nov 29. Clin Cardiol. 2013. PMID: 23197398 Free PMC article.
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