Horie M - Search Results

1

Clinical and electrocardiographic characteristics of patients with short QT interval in a large hospital-based population.

Miyamoto A, Hayashi H, Yoshino T, Kawaguchi T, Taniguchi A, Itoh H, Sugimoto Y, Itoh M, Makiyama T, Xue JQ, Murakami Y, Horie M. Miyamoto A, et al. Among authors: horie m. Heart Rhythm. 2012 Jan;9(1):66-74. doi: 10.1016/j.hrthm.2011.08.016. Epub 2011 Aug 17. Heart Rhythm. 2012. PMID: 21855519

2

Additional gene variants reduce effectiveness of beta-blockers in the LQT1 form of long QT syndrome.

Kobori A, Sarai N, Shimizu W, Nakamura Y, Murakami Y, Makiyama T, Ohno S, Takenaka K, Ninomiya T, Fujiwara Y, Matsuoka S, Takano M, Noma A, Kita T, Horie M. Kobori A, et al. Among authors: horie m. J Cardiovasc Electrophysiol. 2004 Feb;15(2):190-9. doi: 10.1046/j.1540-8167.2004.03212.x. J Cardiovasc Electrophysiol. 2004. PMID: 15028050

3

Double SCN5A mutation underlying asymptomatic Brugada syndrome.

Yokoi H, Makita N, Sasaki K, Takagi Y, Okumura Y, Nishino T, Makiyama T, Kitabatake A, Horie M, Watanabe I, Tsutsui H. Yokoi H, et al. Among authors: horie m. Heart Rhythm. 2005 Mar;2(3):285-92. doi: 10.1016/j.hrthm.2004.11.022. Heart Rhythm. 2005. PMID: 15851320 Free article.

4

High risk for bradyarrhythmic complications in patients with Brugada syndrome caused by SCN5A gene mutations.

Makiyama T, Akao M, Tsuji K, Doi T, Ohno S, Takenaka K, Kobori A, Ninomiya T, Yoshida H, Takano M, Makita N, Yanagisawa F, Higashi Y, Takeyama Y, Kita T, Horie M. Makiyama T, et al. Among authors: horie m. J Am Coll Cardiol. 2005 Dec 6;46(11):2100-6. doi: 10.1016/j.jacc.2005.08.043. Epub 2005 Nov 4. J Am Coll Cardiol. 2005. PMID: 16325048 Free article.

5

Blockade of angiotensin II type 1 receptor improves the arrhythmia morbidity in mice with left ventricular hypertrophy.

Zhang C, Yasuno S, Kuwahara K, Zankov DP, Kobori A, Makiyama T, Horie M. Zhang C, et al. Among authors: horie m. Circ J. 2006 Mar;70(3):335-41. doi: 10.1253/circj.70.335. Circ J. 2006. PMID: 16501302 Free article.

6

Arrhythmogenesis in the short-QT syndrome associated with combined HERG channel gating defects: a simulation study.

Itoh H, Horie M, Ito M, Imoto K. Itoh H, et al. Among authors: horie m. Circ J. 2006 Apr;70(4):502-8. doi: 10.1253/circj.70.502. Circ J. 2006. PMID: 16565572 Free article.

7

Primary malignant lymphoma of the right atrium resulting in superior vena caval syndrome in an HIV-positive patient: depiction at multislice computed tomography and magnetic resonance imaging.

Matsuo S, Sato Y, Miyamoto A, Nakae I, Saeki M, Hodohara K, Horie M. Matsuo S, et al. Among authors: horie m. Cardiovasc Revasc Med. 2006 Oct-Dec;7(4):255-7. doi: 10.1016/j.carrev.2006.03.108. Cardiovasc Revasc Med. 2006. PMID: 17174876

8

Genotype-phenotype correlations of KCNJ2 mutations in Japanese patients with Andersen-Tawil syndrome.

Haruna Y, Kobori A, Makiyama T, Yoshida H, Akao M, Doi T, Tsuji K, Ono S, Nishio Y, Shimizu W, Inoue T, Murakami T, Tsuboi N, Yamanouchi H, Ushinohama H, Nakamura Y, Yoshinaga M, Horigome H, Aizawa Y, Kita T, Horie M. Haruna Y, et al. Among authors: horie m. Hum Mutat. 2007 Feb;28(2):208. doi: 10.1002/humu.9483. Hum Mutat. 2007. PMID: 17221872

9

The association between morning hypertension and metabolic syndrome in hypertensive patients.

Tamaki S, Nakamura Y, Yoshino T, Matsumoto Y, Tarutani Y, Okabayashi T, Kawashima T, Horie M. Tamaki S, et al. Among authors: horie m. Hypertens Res. 2006 Oct;29(10):783-8. doi: 10.1291/hypres.29.783. Hypertens Res. 2006. PMID: 17283865

10

Mechanistic basis for the pathogenesis of long QT syndrome associated with a common splicing mutation in KCNQ1 gene.

Tsuji K, Akao M, Ishii TM, Ohno S, Makiyama T, Takenaka K, Doi T, Haruna Y, Yoshida H, Nakashima T, Kita T, Horie M. Tsuji K, et al. Among authors: horie m. J Mol Cell Cardiol. 2007 Mar;42(3):662-9. doi: 10.1016/j.yjmcc.2006.12.015. Epub 2007 Jan 5. J Mol Cell Cardiol. 2007. PMID: 17292394

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