Miki T - Search Results

1

Pharmacogenetic interactions between Angiotensin-converting enzyme insertion/deletion polymorphism and response to cibenzoline in patients with hypertrophic obstructive cardiomyopathy.

Ogimoto A, Okayama H, Nagai T, Ohtsuka T, Suzuki J, Inoue K, Nishimura K, Saito M, Shigematsu Y, Hamada M, Miki T, Higaki J. Ogimoto A, et al. Among authors: miki t. J Cardiovasc Pharmacol. 2010 May;55(5):506-10. doi: 10.1097/FJC.0b013e3181d8bc4b. J Cardiovasc Pharmacol. 2010. PMID: 20179607 Clinical Trial.

2

Relation between angiotensin-converting enzyme II genotype and atrial fibrillation in Japanese patients with hypertrophic cardiomyopathy.

Ogimoto A, Hamada M, Nakura J, Miki T, Hiwada K. Ogimoto A, et al. Among authors: miki t. J Hum Genet. 2002;47(4):184-9. doi: 10.1007/s100380200021. J Hum Genet. 2002. PMID: 12166654

3

Endothelial nitric oxide synthase gene polymorphism (Glu298Asp) in patients with coexistent hypertrophic cardiomyopathy and coronary spastic angina.

Ogimoto A, Shigematsu Y, Nakura J, Hara Y, Ohtsuka T, Kohara K, Hamada M, Miki T, Higaki J. Ogimoto A, et al. Among authors: miki t. J Mol Med (Berl). 2005 Aug;83(8):619-25. doi: 10.1007/s00109-005-0641-9. Epub 2005 Mar 19. J Mol Med (Berl). 2005. PMID: 15778808

4

A985G polymorphism of the endothelin-2 gene and atrial fibrillation in patients with hypertrophic cardiomyopathy.

Nagai T, Ogimoto A, Okayama H, Ohtsuka T, Shigematsu Y, Hamada M, Miki T, Higaki J. Nagai T, et al. Among authors: miki t. Circ J. 2007 Dec;71(12):1932-6. doi: 10.1253/circj.71.1932. Circ J. 2007. PMID: 18037749 Free article.

5

Association of monocyte chemoattractant protein 1 gene polymorphism with susceptibility to nonfamilial idiopathic dilated cardiomyopathy.

Ogimoto A, Okayama H, Nagai T, Ohtsuka T, Suzuki J, Inoue K, Nishimura K, Shigematsu Y, Tabara Y, Kohara K, Miki T, Higaki J. Ogimoto A, et al. Among authors: miki t. J Cardiol. 2009 Aug;54(1):66-70. doi: 10.1016/j.jjcc.2009.04.001. Epub 2009 May 13. J Cardiol. 2009. PMID: 19632522 Free article.

6

Association Between Genetic Variation in the SCN10A Gene and Cardiac Conduction Abnormalities in Patients With Hypertrophic Cardiomyopathy.

Iio C, Ogimoto A, Nagai T, Suzuki J, Inoue K, Nishimura K, Uetani T, Okayama H, Okura T, Shigematsu Y, Tabara Y, Kohara K, Miki T, Hamada M, Higaki J. Iio C, et al. Among authors: miki t. Int Heart J. 2015;56(4):421-7. doi: 10.1536/ihj.14-411. Epub 2015 Jun 24. Int Heart J. 2015. PMID: 26104176 Free article.

7

17-year follow-up study of a patient with obstructive hypertrophic cardiomyopathy with a deletion mutation in the cardiac myosin binding protein C gene.

Ogimoto A, Hamada M, Nakura J, Shigematsu Y, Hara Y, Ohtsuka T, Morishima A, Kimura A, Miki T, Hiwada K. Ogimoto A, et al. Among authors: miki t. Circ J. 2004 Feb;68(2):174-7. doi: 10.1253/circj.68.174. Circ J. 2004. PMID: 14745156 Free article.

8

Impact of synergistic polymorphisms in adrenergic receptor-related genes and cardiovascular events in patients with dilated cardiomyopathy.

Ogimoto A, Okayama H, Nagai T, Suzuki J, Inoue K, Nishimura K, Shigematsu Y, Tabara Y, Miki T, Higaki J. Ogimoto A, et al. Among authors: miki t. Circ J. 2012;76(8):2003-8. doi: 10.1253/circj.cj-11-1014. Epub 2012 May 12. Circ J. 2012. PMID: 22664639 Free article. Clinical Trial.

9

Angiotensin I-converting enzyme insertion/insertion genotype as a genetic risk factor for cardiovascular disease.

Ogimoto A, Hamada M, Miki T, Higaki J. Ogimoto A, et al. Among authors: miki t. Am Heart J. 2005 Jul;150(1):e1; author reply e3. doi: 10.1016/j.ahj.2004.05.063. Am Heart J. 2005. PMID: 16084135 No abstract available.

10

Polymorphism of inhibitory renin-angiotensin system as a genetic risk factor for atrial fibrillation.

Ogimoto A, Higaki J, Miki T. Ogimoto A, et al. Among authors: miki t. Circulation. 2004 Sep 28;110(13):e329; author reply e329. doi: 10.1161/01.CIR.0000142882.58972.51. Circulation. 2004. PMID: 15451813 No abstract available.

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