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Human genetics and its impact on cardiovascular disease.
Tada H, Fujino N, Hayashi K, Kawashiri MA, Takamura M. Tada H, et al. Among authors: hayashi k. J Cardiol. 2022 Feb;79(2):233-239. doi: 10.1016/j.jjcc.2021.09.005. Epub 2021 Oct 20. J Cardiol. 2022. PMID: 34551866 Free article. Review.
A novel missense mutation in the myosin binding protein-C gene is responsible for hypertrophic cardiomyopathy with left ventricular dysfunction and dilation in elderly patients.
Konno T, Shimizu M, Ino H, Matsuyama T, Yamaguchi M, Terai H, Hayashi K, Mabuchi T, Kiyama M, Sakata K, Hayashi T, Inoue M, Kaneda T, Mabuchi H. Konno T, et al. Among authors: hayashi k, hayashi t. J Am Coll Cardiol. 2003 Mar 5;41(5):781-6. doi: 10.1016/s0735-1097(02)02957-1. J Am Coll Cardiol. 2003. PMID: 12628722 Free article.
[Restrictive cardiomyopathy associated with heart failure].
Konno T, Ino H, Fujino N, Hayashi K, Yamagishi M. Konno T, et al. Among authors: hayashi k. Nihon Rinsho. 2007 May 28;65 Suppl 5:430-7. Nihon Rinsho. 2007. PMID: 17571415 Review. Japanese. No abstract available.
Assessment of QT intervals and prevalence of short QT syndrome in Japan.
Funada A, Hayashi K, Ino H, Fujino N, Uchiyama K, Sakata K, Masuta E, Sakamoto Y, Tsubokawa T, Yamagishi M. Funada A, et al. Among authors: hayashi k. Clin Cardiol. 2008 Jun;31(6):270-4. doi: 10.1002/clc.20208. Clin Cardiol. 2008. PMID: 18543308 Free PMC article.
Impact of QT variables on clinical outcome of genotyped hypertrophic cardiomyopathy.
Uchiyama K, Hayashi K, Fujino N, Konno T, Sakamoto Y, Sakata K, Kawashiri MA, Ino H, Yamagishi M. Uchiyama K, et al. Among authors: hayashi k. Ann Noninvasive Electrocardiol. 2009 Jan;14(1):65-71. doi: 10.1111/j.1542-474X.2008.00275.x. Ann Noninvasive Electrocardiol. 2009. PMID: 19149795 Free PMC article.
8,733 results