Sakurada H - Search Results

1

Genomic organization and mutational analysis of HERG, a gene responsible for familial long QT syndrome.

Itoh T, Tanaka T, Nagai R, Kamiya T, Sawayama T, Nakayama T, Tomoike H, Sakurada H, Yazaki Y, Nakamura Y. Itoh T, et al. Among authors: sakurada h. Hum Genet. 1998 Apr;102(4):435-9. doi: 10.1007/s004390050717. Hum Genet. 1998. PMID: 9600240

2

Voltage-shift of the current activation in HERG S4 mutation (R534C) in LQT2.

Nakajima T, Furukawa T, Hirano Y, Tanaka T, Sakurada H, Takahashi T, Nagai R, Itoh T, Katayama Y, Nakamura Y, Hiraoka M. Nakajima T, et al. Among authors: sakurada h. Cardiovasc Res. 1999 Nov;44(2):283-93. doi: 10.1016/s0008-6363(99)00195-9. Cardiovasc Res. 1999. PMID: 10690305

3

Correlation of genetic etiology with response to beta-adrenergic blockade among symptomatic patients with familial long-QT syndrome.

Itoh T, Kikuchi K, Odagawa Y, Takata S, Yano K, Okada S, Haneda N, Ogawa S, Nakano O, Kawahara Y, Kasai H, Nakayama T, Fukutomi T, Sakurada H, Shimizu A, Yazaki Y, Nagai R, Nakamura Y, Tanaka T. Itoh T, et al. Among authors: sakurada h. J Hum Genet. 2001;46(1):38-40. doi: 10.1007/s100380170123. J Hum Genet. 2001. PMID: 11289718

4

Genotype-Phenotype Correlation of SCN5A Mutation for the Clinical and Electrocardiographic Characteristics of Probands With Brugada Syndrome: A Japanese Multicenter Registry.

Yamagata K, Horie M, Aiba T, Ogawa S, Aizawa Y, Ohe T, Yamagishi M, Makita N, Sakurada H, Tanaka T, Shimizu A, Hagiwara N, Kishi R, Nakano Y, Takagi M, Makiyama T, Ohno S, Fukuda K, Watanabe H, Morita H, Hayashi K, Kusano K, Kamakura S, Yasuda S, Ogawa H, Miyamoto Y, Kapplinger JD, Ackerman MJ, Shimizu W. Yamagata K, et al. Among authors: sakurada h. Circulation. 2017 Jun 6;135(23):2255-2270. doi: 10.1161/CIRCULATIONAHA.117.027983. Epub 2017 Mar 24. Circulation. 2017. PMID: 28341781

5

A novel SCN5A mutation associated with idiopathic ventricular fibrillation without typical ECG findings of Brugada syndrome.

Akai J, Makita N, Sakurada H, Shirai N, Ueda K, Kitabatake A, Nakazawa K, Kimura A, Hiraoka M. Akai J, et al. Among authors: sakurada h. FEBS Lett. 2000 Aug 11;479(1-2):29-34. doi: 10.1016/s0014-5793(00)01875-5. FEBS Lett. 2000. PMID: 10940383 Free article.

6

Novel SCN3B mutation associated with brugada syndrome affects intracellular trafficking and function of Nav1.5.

Ishikawa T, Takahashi N, Ohno S, Sakurada H, Nakamura K, On YK, Park JE, Makiyama T, Horie M, Arimura T, Makita N, Kimura A. Ishikawa T, et al. Among authors: sakurada h. Circ J. 2013;77(4):959-67. doi: 10.1253/circj.cj-12-0995. Epub 2012 Dec 21. Circ J. 2013. PMID: 23257389 Free article. Clinical Trial.

7

Impact of Blood Pressure Visit-to-Visit Variability on Adverse Events in Patients With Nonvalvular Atrial Fibrillation: Subanalysis of the J-RHYTHM Registry.

Kodani E, Inoue H, Atarashi H, Okumura K, Yamashita T, Otsuka T, Origasa H; J‐RHYTHM Registry Investigators *. Kodani E, et al. J Am Heart Assoc. 2021 Jan 5;10(1):e018585. doi: 10.1161/JAHA.120.018585. Epub 2020 Dec 29. J Am Heart Assoc. 2021. PMID: 33372541 Free PMC article.

8

Electrocardiographic features in a patient with the coexistence of long QT syndrome and coronary vasospasm.

Tanaka Y, Nishizaki M, Yamawake N, Sakurada H, Hiraoka M. Tanaka Y, et al. Among authors: sakurada h. Pacing Clin Electrophysiol. 2008 Aug;31(8):1065-9. doi: 10.1111/j.1540-8159.2008.01137.x. Pacing Clin Electrophysiol. 2008. PMID: 18684266

9

A novel disease gene for Brugada syndrome: sarcolemmal membrane-associated protein gene mutations impair intracellular trafficking of hNav1.5.

Ishikawa T, Sato A, Marcou CA, Tester DJ, Ackerman MJ, Crotti L, Schwartz PJ, On YK, Park JE, Nakamura K, Hiraoka M, Nakazawa K, Sakurada H, Arimura T, Makita N, Kimura A. Ishikawa T, et al. Among authors: sakurada h. Circ Arrhythm Electrophysiol. 2012 Dec;5(6):1098-107. doi: 10.1161/CIRCEP.111.969972. Epub 2012 Oct 12. Circ Arrhythm Electrophysiol. 2012. PMID: 23064965

10

Effects of glucose-induced insulin secretion on ventricular repolarization in patients with congenital long QT syndrome.

Nishizaki M, Ashikaga T, Yamawake N, Fujii H, Arita M, Sumitomo N, Sakurada H, Hiraoka M. Nishizaki M, et al. Among authors: sakurada h. Circ J. 2002 Jan;66(1):35-40. doi: 10.1253/circj.66.35. Circ J. 2002. PMID: 11999663 Free article.

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