Makiyama T - Search Results

1

Clinical impact of left ventricular outflow tract obstruction in takotsubo cardiomyopathy.

Kawaji T, Shiomi H, Morimoto T, Tazaki J, Imai M, Saito N, Makiyama T, Shizuta S, Ono K, Kimura T. Kawaji T, et al. Among authors: makiyama t. Circ J. 2015;79(4):839-46. doi: 10.1253/circj.CJ-14-1148. Epub 2015 Jan 28. Circ J. 2015. PMID: 25739572 Free article.

2

[Severe arrythmic events triggered by fever in a case of Brugada syndrome].

Hanazawa K, Tamura T, Doi T, Shizuta S, Makiyama T, Furukawa Y, Nakagawa Y, Kita T, Akao M, Kimura T. Hanazawa K, et al. Among authors: makiyama t. Nihon Naika Gakkai Zasshi. 2007 Nov 10;96(11):2516-8. doi: 10.2169/naika.96.2516. Nihon Naika Gakkai Zasshi. 2007. PMID: 18069304 Japanese. No abstract available.

3

A novel mutation associated with Jervell and Lange-Nielsen syndrome in a Japanese family.

Ohno S, Kubota T, Yoshida H, Tsuji K, Makiyama T, Yamada S, Kuga K, Yamaguchi I, Kita T, Horie M. Ohno S, et al. Among authors: makiyama t. Circ J. 2008 May;72(5):687-93. doi: 10.1253/circj.72.687. Circ J. 2008. PMID: 18441444 Free article.

4

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

5

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. 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.

6

A novel SCN5A gain-of-function mutation M1875T associated with familial atrial fibrillation.

Makiyama T, Akao M, Shizuta S, Doi T, Nishiyama K, Oka Y, Ohno S, Nishio Y, Tsuji K, Itoh H, Kimura T, Kita T, Horie M. Makiyama T, et al. J Am Coll Cardiol. 2008 Oct 14;52(16):1326-34. doi: 10.1016/j.jacc.2008.07.013. J Am Coll Cardiol. 2008. PMID: 18929244 Free article.

7

Dynamic change in ST-segment and spontaneous occurrence of ventricular fibrillation in Brugada syndrome with a novel nonsense mutation in the SCN5A gene during long-term follow-up.

Kawamura M, Ozawa T, Yao T, Ashihara T, Sugimoto Y, Yagi T, Itoh H, Ito M, Makiyama T, Horie M. Kawamura M, et al. Among authors: makiyama t. Circ J. 2009 Mar;73(3):584-8. doi: 10.1253/circj.cj-08-0142. Epub 2008 Dec 12. Circ J. 2009. PMID: 19075524 Free article.

8

Impact of CYP2C19 polymorphisms on the antiplatelet effect of clopidogrel in an actual clinical setting in Japan.

Jinnai T, Horiuchi H, Makiyama T, Tazaki J, Tada T, Akao M, Ono K, Hoshino K, Naruse Y, Takahashi K, Watanabe H, Kita T, Kimura T. Jinnai T, et al. Among authors: makiyama t. Circ J. 2009 Aug;73(8):1498-503. doi: 10.1253/circj.cj-09-0019. Epub 2009 Jun 17. Circ J. 2009. PMID: 19531897 Free article.

9

D85N, a KCNE1 polymorphism, is a disease-causing gene variant in long QT syndrome.

Nishio Y, Makiyama T, Itoh H, Sakaguchi T, Ohno S, Gong YZ, Yamamoto S, Ozawa T, Ding WG, Toyoda F, Kawamura M, Akao M, Matsuura H, Kimura T, Kita T, Horie M. Nishio Y, et al. Among authors: makiyama t. J Am Coll Cardiol. 2009 Aug 25;54(9):812-9. doi: 10.1016/j.jacc.2009.06.005. J Am Coll Cardiol. 2009. PMID: 19695459 Free article.

10

Risk determinants in individuals with a spontaneous type 1 Brugada ECG.

Miyamoto A, Hayashi H, Makiyama T, Yoshino T, Mizusawa Y, Sugimoto Y, Ito M, Xue JQ, Murakami Y, Horie M. Miyamoto A, et al. Among authors: makiyama t. Circ J. 2011;75(4):844-51. doi: 10.1253/circj.cj-10-0903. Epub 2011 Feb 18. Circ J. 2011. PMID: 21343656 Free article.

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