Miyamoto Y - Search Results

1

Exome Analyses of Long QT Syndrome Reveal Candidate Pathogenic Mutations in Calmodulin-Interacting Genes.

Shigemizu D, Aiba T, Nakagawa H, Ozaki K, Miya F, Satake W, Toda T, Miyamoto Y, Fujimoto A, Suzuki Y, Kubo M, Tsunoda T, Shimizu W, Tanaka T. Shigemizu D, et al. Among authors: miyamoto y. PLoS One. 2015 Jul 1;10(7):e0130329. doi: 10.1371/journal.pone.0130329. eCollection 2015. PLoS One. 2015. PMID: 26132555 Free PMC article.

2

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.

3

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.

4

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.

5

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

6

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.

7

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

8

Genotype-phenotype aspects of type 2 long QT syndrome.

Shimizu W, Moss AJ, Wilde AA, Towbin JA, Ackerman MJ, January CT, Tester DJ, Zareba W, Robinson JL, Qi M, Vincent GM, Kaufman ES, Hofman N, Noda T, Kamakura S, Miyamoto Y, Shah S, Amin V, Goldenberg I, Andrews ML, McNitt S. Shimizu W, et al. Among authors: miyamoto y. J Am Coll Cardiol. 2009 Nov 24;54(22):2052-62. doi: 10.1016/j.jacc.2009.08.028. J Am Coll Cardiol. 2009. PMID: 19926013 Free PMC article.

9

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

10

Heart rate-dependent variability of cardiac events in type 2 congenital long-QT syndrome.

Nagaoka I, Shimizu W, Mizusawa Y, Sakaguchi T, Itoh H, Ohno S, Makiyama T, Yamagata K, Makimoto H, Miyamoto Y, Kamakura S, Horie M. Nagaoka I, et al. Among authors: miyamoto y. Europace. 2010 Nov;12(11):1623-9. doi: 10.1093/europace/euq342. Epub 2010 Sep 29. Europace. 2010. PMID: 20880952

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