Miyamoto Y - Search Results

1

Long QT syndrome with compound mutations is associated with a more severe phenotype: a Japanese multicenter study.

Itoh H, Shimizu W, Hayashi K, Yamagata K, Sakaguchi T, Ohno S, Makiyama T, Akao M, Ai T, Noda T, Miyazaki A, Miyamoto Y, Yamagishi M, Kamakura S, Horie M. Itoh H, et al. Among authors: miyamoto y. Heart Rhythm. 2010 Oct;7(10):1411-8. doi: 10.1016/j.hrthm.2010.06.013. Epub 2010 Jun 9. Heart Rhythm. 2010. PMID: 20541041

2

Plasma levels of brain and atrial natriuretic peptides elevate in proportion to left ventricular end-systolic wall stress in patients with aortic stenosis.

Ikeda T, Matsuda K, Itoh H, Shirakami G, Miyamoto Y, Yoshimasa T, Nakao K, Ban T. Ikeda T, et al. Among authors: miyamoto y. Am Heart J. 1997 Mar;133(3):307-14. doi: 10.1016/s0002-8703(97)70225-4. Am Heart J. 1997. PMID: 9060799

3

Frequency and clinical characteristics of dilated cardiomyopathy caused by desmin gene mutation in a Japanese population.

Miyamoto Y, Akita H, Shiga N, Takai E, Iwai C, Mizutani K, Kawai H, Takarada A, Yokoyama M. Miyamoto Y, et al. Eur Heart J. 2001 Dec;22(24):2284-9. doi: 10.1053/euhj.2001.2836. Eur Heart J. 2001. PMID: 11728149

4

Mutation site-specific differences in arrhythmic risk and sensitivity to sympathetic stimulation in the LQT1 form of congenital long QT syndrome: multicenter study in Japan.

Shimizu W, Horie M, Ohno S, Takenaka K, Yamaguchi M, Shimizu M, Washizuka T, Aizawa Y, Nakamura K, Ohe T, Aiba T, Miyamoto Y, Yoshimasa Y, Towbin JA, Priori SG, Kamakura S. Shimizu W, et al. Among authors: miyamoto y. J Am Coll Cardiol. 2004 Jul 7;44(1):117-25. doi: 10.1016/j.jacc.2004.03.043. J Am Coll Cardiol. 2004. PMID: 15234419 Free article.

5

Diagnostic value of epinephrine test for genotyping LQT1, LQT2, and LQT3 forms of congenital long QT syndrome.

Shimizu W, Noda T, Takaki H, Nagaya N, Satomi K, Kurita T, Suyama K, Aihara N, Sunagawa K, Echigo S, Miyamoto Y, Yoshimasa Y, Nakamura K, Ohe T, Towbin JA, Priori SG, Kamakura S. Shimizu W, et al. Among authors: miyamoto y. Heart Rhythm. 2004 Sep;1(3):276-83. doi: 10.1016/j.hrthm.2004.04.021. Heart Rhythm. 2004. PMID: 15851169 Clinical Trial.

6

Common sodium channel promoter haplotype in asian subjects underlies variability in cardiac conduction.

Bezzina CR, Shimizu W, Yang P, Koopmann TT, Tanck MW, Miyamoto Y, Kamakura S, Roden DM, Wilde AA. Bezzina CR, et al. Among authors: miyamoto y. Circulation. 2006 Jan 24;113(3):338-44. doi: 10.1161/CIRCULATIONAHA.105.580811. Epub 2006 Jan 16. Circulation. 2006. PMID: 16415376

7

Clinical aspects of type-1 long-QT syndrome by location, coding type, and biophysical function of mutations involving the KCNQ1 gene.

Moss AJ, Shimizu W, Wilde AA, Towbin JA, Zareba W, Robinson JL, Qi M, Vincent GM, Ackerman MJ, Kaufman ES, Hofman N, Seth R, Kamakura S, Miyamoto Y, Goldenberg I, Andrews ML, McNitt S. Moss AJ, et al. Among authors: miyamoto y. Circulation. 2007 May 15;115(19):2481-9. doi: 10.1161/CIRCULATIONAHA.106.665406. Epub 2007 Apr 30. Circulation. 2007. PMID: 17470695 Free PMC article.

8

Age- and genotype-specific triggers for life-threatening arrhythmia in the genotyped long QT syndrome.

Sakaguchi T, Shimizu W, Itoh H, Noda T, Miyamoto Y, Nagaoka I, Oka Y, Ashihara T, Ito M, Tsuji K, Ohno S, Makiyama T, Kamakura S, Horie M. Sakaguchi T, et al. Among authors: miyamoto y. J Cardiovasc Electrophysiol. 2008 Aug;19(8):794-9. doi: 10.1111/j.1540-8167.2008.01138.x. Epub 2008 Mar 26. J Cardiovasc Electrophysiol. 2008. PMID: 18373596

9

Mutation site dependent variability of cardiac events in Japanese LQT2 form of congenital long-QT syndrome.

Nagaoka I, Shimizu W, Itoh H, Yamamoto S, Sakaguchi T, Oka Y, Tsuji K, Ashihara T, Ito M, Yoshida H, Ohno S, Makiyama T, Miyamoto Y, Noda T, Kamakura S, Akao M, Horie M. Nagaoka I, et al. Among authors: miyamoto y. Circ J. 2008 May;72(5):694-9. doi: 10.1253/circj.72.694. Circ J. 2008. PMID: 18441445 Free article.

10

Novel KCNE3 mutation reduces repolarizing potassium current and associated with long QT syndrome.

Ohno S, Toyoda F, Zankov DP, Yoshida H, Makiyama T, Tsuji K, Honda T, Obayashi K, Ueyama H, Shimizu W, Miyamoto Y, Kamakura S, Matsuura H, Kita T, Horie M. Ohno S, et al. Among authors: miyamoto y. Hum Mutat. 2009 Apr;30(4):557-63. doi: 10.1002/humu.20834. Hum Mutat. 2009. PMID: 19306396

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