Miki T - Search Results

1

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.

2

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.

3

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.

4

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.

5

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

6

Association of endothelin-1 gene variant with hypertension.

Jin JJ, Nakura J, Wu Z, Yamamoto M, Abe M, Tabara Y, Yamamoto Y, Igase M, Kohara K, Miki T. Jin JJ, et al. Among authors: miki t. Hypertension. 2003 Jan;41(1):163-7. doi: 10.1161/01.hyp.0000043680.75107.cf. Hypertension. 2003. PMID: 12511547

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

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

9

Genotype risk score of common susceptible variants for prediction of type 2 diabetes mellitus in Japanese: the Shimanami Health Promoting Program (J-SHIPP study). Development of type 2 diabetes mellitus and genotype risk score.

Tabara Y, Osawa H, Kawamoto R, Onuma H, Shimizu I, Makino H, Kohara K, Miki T. Tabara Y, et al. Among authors: miki t. Metabolism. 2011 Nov;60(11):1634-40. doi: 10.1016/j.metabol.2011.03.014. Epub 2011 May 6. Metabolism. 2011. PMID: 21550079

10

The Association between Hypertension and Dementia in the Elderly.

Igase M, Kohara K, Miki T. Igase M, et al. Among authors: miki t. Int J Hypertens. 2012;2012:320648. doi: 10.1155/2012/320648. Epub 2011 Nov 3. Int J Hypertens. 2012. PMID: 22121477 Free PMC article.

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