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

Year Number of Results
1976 2
1982 1
1983 1
1987 1
1990 2
1997 1
1998 1
2002 40
2003 44
2004 49
2005 64
2006 61
2007 50
2008 48
2009 49
2010 57
2011 59
2012 69
2013 81
2014 66
2015 51
2016 69
2017 74
2018 57
2019 61
2020 54
2021 44
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1,033 results
Results by year
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Page 1
Potential therapeutic interventions for chronic kidney disease-associated sarcopenia via indoxyl sulfate-induced mitochondrial dysfunction.
Enoki Y, Watanabe H, Arake R, Fujimura R, Ishiodori K, Imafuku T, Nishida K, Sugimoto R, Nagao S, Miyamura S, Ishima Y, Tanaka M, Matsushita K, Komaba H, Fukagawa M, Otagiri M, Maruyama T. Enoki Y, et al. Among authors: watanabe h. J Cachexia Sarcopenia Muscle. 2017 Oct;8(5):735-747. doi: 10.1002/jcsm.12202. Epub 2017 Jun 12. J Cachexia Sarcopenia Muscle. 2017. PMID: 28608457 Free PMC article.
Association of Genetic and Clinical Aspects of Congenital Long QT Syndrome With Life-Threatening Arrhythmias in Japanese Patients.
Shimizu W, Makimoto H, Yamagata K, Kamakura T, Wada M, Miyamoto K, Inoue-Yamada Y, Okamura H, Ishibashi K, Noda T, Nagase S, Miyazaki A, Sakaguchi H, Shiraishi I, Makiyama T, Ohno S, Itoh H, Watanabe H, Hayashi K, Yamagishi M, Morita H, Yoshinaga M, Aizawa Y, Kusano K, Miyamoto Y, Kamakura S, Yasuda S, Ogawa H, Tanaka T, Sumitomo N, Hagiwara N, Fukuda K, Ogawa S, Aizawa Y, Makita N, Ohe T, Horie M, Aiba T. Shimizu W, et al. Among authors: watanabe h. JAMA Cardiol. 2019 Mar 1;4(3):246-254. doi: 10.1001/jamacardio.2018.4925. JAMA Cardiol. 2019. PMID: 30758498 Free PMC article. Retracted.
Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death.
Bezzina CR, Barc J, Mizusawa Y, Remme CA, Gourraud JB, Simonet F, Verkerk AO, Schwartz PJ, Crotti L, Dagradi F, Guicheney P, Fressart V, Leenhardt A, Antzelevitch C, Bartkowiak S, Borggrefe M, Schimpf R, Schulze-Bahr E, Zumhagen S, Behr ER, Bastiaenen R, Tfelt-Hansen J, Olesen MS, Kääb S, Beckmann BM, Weeke P, Watanabe H, Endo N, Minamino T, Horie M, Ohno S, Hasegawa K, Makita N, Nogami A, Shimizu W, Aiba T, Froguel P, Balkau B, Lantieri O, Torchio M, Wiese C, Weber D, Wolswinkel R, Coronel R, Boukens BJ, Bézieau S, Charpentier E, Chatel S, Despres A, Gros F, Kyndt F, Lecointe S, Lindenbaum P, Portero V, Violleau J, Gessler M, Tan HL, Roden DM, Christoffels VM, Le Marec H, Wilde AA, Probst V, Schott JJ, Dina C, Redon R. Bezzina CR, et al. Among authors: watanabe h. Nat Genet. 2013 Sep;45(9):1044-9. doi: 10.1038/ng.2712. Epub 2013 Jul 21. Nat Genet. 2013. PMID: 23872634 Free PMC article.
Genetics of Brugada syndrome.
Watanabe H, Minamino T. Watanabe H, et al. J Hum Genet. 2016 Jan;61(1):57-60. doi: 10.1038/jhg.2015.97. Epub 2015 Jul 30. J Hum Genet. 2016. PMID: 26223181 Free article. Review.
[Rheumatoid arthritis and viral hepatitis].
Kobayashi H, Watanabe H, Ohira H. Kobayashi H, et al. Among authors: watanabe h. Nihon Rinsho. 2016 Jun;74(6):1007-11. Nihon Rinsho. 2016. PMID: 27311193 Review. Japanese.
1,033 results
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