Horie M - Search Results

1

Differential Diagnosis Between Catecholaminergic Polymorphic Ventricular Tachycardia and Long QT Syndrome Type 1　- Modified Schwartz Score.

Ozawa J, Ohno S, Fujii Y, Makiyama T, Suzuki H, Saitoh A, Horie M. Ozawa J, et al. Among authors: horie m. Circ J. 2018 Aug 24;82(9):2269-2276. doi: 10.1253/circj.CJ-17-1032. Epub 2018 Jun 21. Circ J. 2018. PMID: 29925740 Free article.

2

[On the mechanism of beta-adrenergic activation of cardiac outward currents--chloride and delayed rectifier potassium conductance].

Gadsby DC, Horie M, Makita T, Zang WJ, Suzuki H, Kawai C. Gadsby DC, et al. Among authors: horie m. Jpn Circ J. 1992;56 Suppl 5:1344-8. Jpn Circ J. 1992. PMID: 1337921 Japanese. No abstract available.

3

Successful radiofrequency current catheter ablation of accessory atrioventricular pathway after tricuspid replacement in Ebstein's anomaly.

Ai T, Horie M, Washizuka T, Albrecht C, Nishimoto T, Obayashi K, Tsuchiya K, Watanuki M, Sasayama S. Ai T, et al. Among authors: horie m. Jpn Circ J. 1998 Oct;62(10):791-3. doi: 10.1253/jcj.62.791. Jpn Circ J. 1998. PMID: 9805266 Free article.

4

Novel KCNJ2 mutation in familial periodic paralysis with ventricular dysrhythmia.

Ai T, Fujiwara Y, Tsuji K, Otani H, Nakano S, Kubo Y, Horie M. Ai T, et al. Among authors: horie m. Circulation. 2002 Jun 4;105(22):2592-4. doi: 10.1161/01.cir.0000019906.35135.a3. Circulation. 2002. PMID: 12045162

5

Drug-induced long-QT syndrome associated with a subclinical SCN5A mutation.

Makita N, Horie M, Nakamura T, Ai T, Sasaki K, Yokoi H, Sakurai M, Sakuma I, Otani H, Sawa H, Kitabatake A. Makita N, et al. Among authors: horie m. Circulation. 2002 Sep 3;106(10):1269-74. doi: 10.1161/01.cir.0000027139.42087.b6. Circulation. 2002. PMID: 12208804

6

Exercise stress test amplifies genotype-phenotype correlation in the LQT1 and LQT2 forms of the long-QT syndrome.

Takenaka K, Ai T, Shimizu W, Kobori A, Ninomiya T, Otani H, Kubota T, Takaki H, Kamakura S, Horie M. Takenaka K, et al. Among authors: horie m. Circulation. 2003 Feb 18;107(6):838-44. doi: 10.1161/01.cir.0000048142.85076.a2. Circulation. 2003. PMID: 12591753 Clinical Trial.

7

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

8

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: horie m. 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.

9

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.

10

Myocardial creatine concentration in various nonischemic heart diseases assessed by 1H magnetic resonance spectroscopy.

Nakae I, Mitsunami K, Matsuo S, Inubushi T, Morikawa S, Tsutamoto T, Koh T, Horie M. Nakae I, et al. Among authors: horie m. Circ J. 2005 Jun;69(6):711-6. doi: 10.1253/circj.69.711. Circ J. 2005. PMID: 15914951 Free article.

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