Yamaguchi M - Search Results

1

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. Clin Sci (Lond). 2003 Apr;104(4):377-82. doi: 10.1042/CS20020152. Clin Sci (Lond). 2003. PMID: 12653681

2

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. Among authors: yamaguchi m. Cardiovasc Res. 2002 Apr;54(1):67-76. doi: 10.1016/s0008-6363(02)00240-7. Cardiovasc Res. 2002. PMID: 12062363

3

Q-T peak dispersion in congenital long QT syndrome: possible marker of mutation of HERG.

Inoue M, Shimizu M, Ino H, Yamaguchi M, Terai H, Hayashi K, Kiyama M, Sakata K, Hayashi T, Mabuchi H. Inoue M, et al. Among authors: yamaguchi m. Circ J. 2003 Jun;67(6):495-8. doi: 10.1253/circj.67.495. Circ J. 2003. PMID: 12808265 Free article.

4

T wave peak-to-end interval and QT dispersion in acquired long QT syndrome: a new index for arrhythmogenicity.

Yamaguchi M, Shimizu M, Ino H, Terai H, Uchiyama K, Oe K, Mabuchi T, Konno T, Kaneda T, Mabuchi H. Yamaguchi M, et al. Clin Sci (Lond). 2003 Dec;105(6):671-6. doi: 10.1042/CS20030010. Clin Sci (Lond). 2003. PMID: 12857349

5

Probucol aggravates long QT syndrome associated with a novel missense mutation M124T in the N-terminus of HERG.

Hayashi K, Shimizu M, Ino H, Yamaguchi M, Terai H, Hoshi N, Higashida H, Terashima N, Uno Y, Kanaya H, Mabuchi H. Hayashi K, et al. Among authors: yamaguchi m. Clin Sci (Lond). 2004 Aug;107(2):175-82. doi: 10.1042/CS20030351. Clin Sci (Lond). 2004. PMID: 15043509

6

Compound heterozygosity for mutations Asp611-->Tyr in KCNQ1 and Asp609-->Gly in KCNH2 associated with severe long QT syndrome.

Yamaguchi M, Shimizu M, Ino H, Terai H, Hayashi K, Kaneda T, Mabuchi H, Sumita R, Oshima T, Hoshi N, Higashida H. Yamaguchi M, et al. Clin Sci (Lond). 2005 Feb;108(2):143-50. doi: 10.1042/CS20040220. Clin Sci (Lond). 2005. PMID: 15500450

7

A novel mutation Lys273Glu in the cardiac troponin T gene shows high degree of penetrance and transition from hypertrophic to dilated cardiomyopathy.

Fujino N, Shimizu M, Ino H, Yamaguchi M, Yasuda T, Nagata M, Konno T, Mabuchi H. Fujino N, et al. Among authors: yamaguchi m. Am J Cardiol. 2002 Jan 1;89(1):29-33. doi: 10.1016/s0002-9149(01)02158-0. Am J Cardiol. 2002. PMID: 11779518

8

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: yamaguchi m. Am Heart J. 2002 Feb;143(2):289-93. doi: 10.1067/mhj.2002.119760. Am Heart J. 2002. PMID: 11835033

9

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: yamaguchi m. Am Heart J. 2002 Apr;143(4):690-5. doi: 10.1067/mhj.2002.120291. Am Heart J. 2002. PMID: 11923807

10

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: yamaguchi m. Circ J. 2002 May;66(5):435-40. doi: 10.1253/circj.66.435. Circ J. 2002. PMID: 12030335 Free article.

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