Komura S - Search Results

1

Human cardiac ryanodine receptor mutations in ion channel disorders in Japan.

Aizawa Y, Mitsuma W, Ikrar T, Komura S, Hanawa H, Miyajima S, Miyoshi F, Kobayashi Y, Chinushi M, Kimura A, Hiraoka M, Aizawa Y. Aizawa Y, et al. Among authors: komura s. Int J Cardiol. 2007 Mar 20;116(2):263-5. doi: 10.1016/j.ijcard.2006.02.024. Epub 2006 Jul 14. Int J Cardiol. 2007. PMID: 16843546

2

A novel mutation in FKBP12.6 binding region of the human cardiac ryanodine receptor gene (R2401H) in a Japanese patient with catecholaminergic polymorphic ventricular tachycardia.

Aizawa Y, Ueda K, Komura S, Washizuka T, Chinushi M, Inagaki N, Matsumoto Y, Hayashi T, Takahashi M, Nakano N, Yasunami M, Kimura A, Hiraoka M, Aizawa Y. Aizawa Y, et al. Among authors: komura s. Int J Cardiol. 2005 Mar 18;99(2):343-5. doi: 10.1016/j.ijcard.2003.11.050. Int J Cardiol. 2005. PMID: 15749201

3

Distinct U wave changes in patients with catecholaminergic polymorphic ventricular tachycardia (CPVT).

Aizawa Y, Komura S, Okada S, Chinushi M, Aizawa Y, Morita H, Ohe T. Aizawa Y, et al. Among authors: komura s. Int Heart J. 2006 May;47(3):381-9. doi: 10.1536/ihj.47.381. Int Heart J. 2006. PMID: 16823244 Free article.

4

Function, subcellular localization and assembly of a novel mutation of KCNJ2 in Andersen's syndrome.

Hosaka Y, Hanawa H, Washizuka T, Chinushi M, Yamashita F, Yoshida T, Komura S, Watanabe H, Aizawa Y. Hosaka Y, et al. Among authors: komura s. J Mol Cell Cardiol. 2003 Apr;35(4):409-15. doi: 10.1016/s0022-2828(03)00046-4. J Mol Cell Cardiol. 2003. PMID: 12689820

5

Incidence and initial characteristics of pilsicainide-induced ventricular arrhythmias in patients with Brugada syndrome.

Chinushi M, Komura S, Izumi D, Furushima H, Tanabe Y, Washizuka T, Aizawa Y. Chinushi M, et al. Among authors: komura s. Pacing Clin Electrophysiol. 2007 May;30(5):662-71. doi: 10.1111/j.1540-8159.2007.00728.x. Pacing Clin Electrophysiol. 2007. PMID: 17461877

6

A double-point mutation in the selectivity filter site of the KCNQ1 potassium channel results in a severe phenotype, LQT1, of long QT syndrome.

Ikrar T, Hanawa H, Watanabe H, Okada S, Aizawa Y, Ramadan MM, Komura S, Yamashita F, Chinushi M, Aizawa Y. Ikrar T, et al. Among authors: komura s. J Cardiovasc Electrophysiol. 2008 May;19(5):541-9. doi: 10.1111/j.1540-8167.2007.01076.x. Epub 2008 Feb 4. J Cardiovasc Electrophysiol. 2008. PMID: 18266681

7

Decrease in amplitude of intracardiac ventricular electrogram and inappropriate therapy in patients with an implantable cardioverter defibrillator.

Watanabe H, Chinushi M, Izumi D, Sato A, Okada S, Okamura K, Komura S, Hosaka Y, Furushima H, Washizuka T, Aizawa Y. Watanabe H, et al. Among authors: komura s. Int Heart J. 2006 May;47(3):363-70. doi: 10.1536/ihj.47.363. Int Heart J. 2006. PMID: 16823242 Free article.

8

Endocardial arrhythmogenic mechanisms of torsades de pointes in patients with the congenital long QT syndrome.

Chinushi M, Furushima H, Hosaka Y, Komura S, Sato A, Iijima K, Aizawa Y. Chinushi M, et al. Among authors: komura s. Intern Med. 2011;50(16):1695-702. doi: 10.2169/internalmedicine.50.5114. Epub 2011 Aug 15. Intern Med. 2011. PMID: 21841328 Free article.

9

Comparison of conduction delay in the right ventricular outflow tract between Brugada syndrome and right ventricular cardiomyopathy: investigation of signal average ECG in the precordial leads.

Furushima H, Chinushi M, Okamura K, Iijima K, Komura S, Tanabe Y, Okada S, Izumi D, Aizawa Y. Furushima H, et al. Among authors: komura s. Europace. 2007 Oct;9(10):951-6. doi: 10.1093/europace/eum128. Epub 2007 Jul 17. Europace. 2007. PMID: 17636305

10

Antiarrhythmic vs. pro-arrhythmic effects depending on the intensity of adrenergic stimulation in a canine anthopleurin-A model of type-3 long QT syndrome.

Chinushi M, Izumi D, Iijima K, Ahara S, Komura S, Furushima H, Hosaka Y, Aizawa Y. Chinushi M, et al. Among authors: komura s. Europace. 2008 Feb;10(2):249-55. doi: 10.1093/europace/eun002. Europace. 2008. PMID: 18256131

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