Hayashi K - Search Results

1

Septal wall thinning and systolic dysfunction in patients with hypertrophic cardiomyopathy caused by a cardiac troponin I gene mutation.

Shimizu M, Ino H, Okeie K, Yamaguchi M, Hayashi K, Nagata M, Itoh H, Iwaki T, Oe K, Konno T, Mabuchi H. Shimizu M, et al. Among authors: hayashi k. Am Heart J. 2002 Apr;143(4):690-5. doi: 10.1067/mhj.2002.120291. Am Heart J. 2002. PMID: 11923807

2

Heterogeneity of cardiac sympathetic nerve activity and systolic dysfunction in patients with hypertrophic cardiomyopathy.

Shimizu M, Ino H, Yamaguchi M, Terai H, Hayashi K, Nakajima K, Taki J, Mabuchi H. Shimizu M, et al. Among authors: hayashi k. J Nucl Med. 2002 Jan;43(1):15-20. J Nucl Med. 2002. PMID: 11801697 Free article.

3

Chronologic electrocardiographic changes in patients with hypertrophic cardiomyopathy associated with cardiac troponin 1 mutation.

Shimizu M, Ino H, Yamaguchi M, Terai H, Hayashi K, Kiyama M, Sakata K, Hayashi T, Inoue M, Kaneda T, Mabuchi H. Shimizu M, et al. Among authors: hayashi k, hayashi t. Am Heart J. 2002 Feb;143(2):289-93. doi: 10.1067/mhj.2002.119760. Am Heart J. 2002. PMID: 11835033

4

Effects of gender on the number of diseased vessels and clinical outcome in Japanese patients with acute coronary syndrome.

Oe K, Shimizu M, Ino H, Yamaguchi M, Terai H, Hayashi K, Kiyama M, Sakata K, Hayashi T, Inoue M, Kaneda T, Mabuchi H. Oe K, et al. Among authors: hayashi k, hayashi t. Circ J. 2002 May;66(5):435-40. doi: 10.1253/circj.66.435. Circ J. 2002. PMID: 12030335 Free article.

5

Characterization of a novel missense mutation E637K in the pore-S6 loop of HERG in a patient with long QT syndrome.

Hayashi K, Shimizu M, Ino H, Yamaguchi M, Mabuchi H, Hoshi N, Higashida H. Hayashi K, et al. Cardiovasc Res. 2002 Apr;54(1):67-76. doi: 10.1016/s0008-6363(02)00240-7. Cardiovasc Res. 2002. PMID: 12062363

6

T-peak to T-end interval may be a better predictor of high-risk patients with hypertrophic cardiomyopathy associated with a cardiac troponin I mutation than QT dispersion.

Shimizu M, Ino H, Okeie K, Yamaguchi M, Nagata M, Hayashi K, Itoh H, Iwaki T, Oe K, Konno T, Mabuchi H. Shimizu M, et al. Among authors: hayashi k. Clin Cardiol. 2002 Jul;25(7):335-9. doi: 10.1002/clc.4950250706. Clin Cardiol. 2002. PMID: 12109867 Free PMC article.

7

In-hospital outcome in octogenarians with acute coronary syndrome undergoing emergent coronary angiography.

Oe K, Shimizu M, Ino H, Yamaguchi M, Terai H, Hayashi K, Kiyama M, Sakata K, Hayashi T, Inoue M, Kaneda T, Mabuchi H. Oe K, et al. Among authors: hayashi k, hayashi t. Jpn Heart J. 2003 Jan;44(1):11-20. doi: 10.1536/jhj.44.11. Jpn Heart J. 2003. PMID: 12622433 Free article.

8

Hemodynamic changes and prognosis in patients with hypertrophic cardiomyopathy and abnormal blood pressure responses during exercise.

Nagata M, Shimizu M, Ino H, Yamaguchi M, Hayashi K, Taki J, Mabuchi H. Nagata M, et al. Among authors: hayashi k. Clin Cardiol. 2003 Feb;26(2):71-6. doi: 10.1002/clc.4960260206. Clin Cardiol. 2003. PMID: 12625597 Free PMC article.

9

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.

10

Clinical and electrophysiological characterization of a novel mutation (F193L) in the KCNQ1 gene associated with long QT syndrome.

Yamaguchi M, Shimizu M, Ino H, Terai H, Hayashi K, Mabuchi H, Hoshi N, Higashida H. Yamaguchi M, et al. Among authors: hayashi k. Clin Sci (Lond). 2003 Apr;104(4):377-82. doi: 10.1042/CS20020152. Clin Sci (Lond). 2003. PMID: 12653681

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