Ohno S - Search Results

1

An International Multicenter Cohort Study on β-Blockers for the Treatment of Symptomatic Children With Catecholaminergic Polymorphic Ventricular Tachycardia.

Peltenburg PJ, Kallas D, Bos JM, Lieve KVV, Franciosi S, Roston TM, Denjoy I, Sorensen KB, Ohno S, Roses-Noguer F, Aiba T, Maltret A, LaPage MJ, Atallah J, Giudicessi JR, Clur SB, Blom NA, Tanck M, Extramiana F, Kato K, Barc J, Borggrefe M, Behr ER, Sarquella-Brugada G, Tfelt-Hansen J, Zorio E, Swan H, Kammeraad JAE, Krahn AD, Davis A, Sacher F, Schwartz PJ, Roberts JD, Skinner JR, van den Berg MP, Kannankeril PJ, Drago F, Robyns T, Haugaa K, Tavacova T, Semsarian C, Till J, Probst V, Brugada R, Shimizu W, Horie M, Leenhardt A, Ackerman MJ, Sanatani S, van der Werf C, Wilde AAM. Peltenburg PJ, et al. Among authors: ohno s. Circulation. 2022 Feb;145(5):333-344. doi: 10.1161/CIRCULATIONAHA.121.056018. Epub 2021 Dec 7. Circulation. 2022. PMID: 34874747

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: ohno s. 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

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: ohno s. 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.

4

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: ohno s. 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

5

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: ohno s. Circ J. 2008 May;72(5):694-9. doi: 10.1253/circj.72.694. Circ J. 2008. PMID: 18441445 Free article.

6

Mutation analysis of the glycerol-3 phosphate dehydrogenase-1 like (GPD1L) gene in Japanese patients with Brugada syndrome.

Makiyama T, Akao M, Haruna Y, Tsuji K, Doi T, Ohno S, Nishio Y, Kita T, Horie M. Makiyama T, et al. Among authors: ohno s. Circ J. 2008 Oct;72(10):1705-6. doi: 10.1253/circj.cj-08-0508. Epub 2008 Sep 2. Circ J. 2008. PMID: 18762705 Free article.

7

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: ohno s. 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

8

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: ohno s. Europace. 2010 Nov;12(11):1623-9. doi: 10.1093/europace/euq342. Epub 2010 Sep 29. Europace. 2010. PMID: 20880952

9

Atrioventricular block-induced Torsades de Pointes with clinical and molecular backgrounds similar to congenital long QT syndrome.

Oka Y, Itoh H, Ding WG, Shimizu W, Makiyama T, Ohno S, Nishio Y, Sakaguchi T, Miyamoto A, Kawamura M, Matsuura H, Horie M. Oka Y, et al. Among authors: ohno s. Circ J. 2010 Nov;74(12):2562-71. doi: 10.1253/circj.cj-10-0498. Epub 2010 Oct 21. Circ J. 2010. PMID: 20975234 Free article.

10

Phenotype variability in patients carrying KCNJ2 mutations.

Kimura H, Zhou J, Kawamura M, Itoh H, Mizusawa Y, Ding WG, Wu J, Ohno S, Makiyama T, Miyamoto A, Naiki N, Wang Q, Xie Y, Suzuki T, Tateno S, Nakamura Y, Zang WJ, Ito M, Matsuura H, Horie M. Kimura H, et al. Among authors: ohno s. Circ Cardiovasc Genet. 2012 Jun;5(3):344-53. doi: 10.1161/CIRCGENETICS.111.962316. Epub 2012 May 15. Circ Cardiovasc Genet. 2012. PMID: 22589293

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