Sakata K - Search Results

1

Whole exome sequencing combined with integrated variant annotation prediction identifies asymptomatic Tangier disease with compound heterozygous mutations in ABCA1 gene.

Tada H, Kawashiri MA, Nohara A, Saito R, Tanaka Y, Nomura A, Konno T, Sakata K, Fujino N, Takamura T, Inazu A, Mabuchi H, Yamagishi M, Hayashi K. Tada H, et al. Among authors: sakata k. Atherosclerosis. 2015 Jun;240(2):324-9. doi: 10.1016/j.atherosclerosis.2015.04.003. Epub 2015 Apr 7. Atherosclerosis. 2015. PMID: 25875382

2

Chronologic electrocardiographic changes in patients with hypertrophic cardiomyopathy associated with cardiac troponin 1 mutation.

Shimizu M, Ino H, Yamaguchi M, Terai H, Hayashi K, Kiyama M, Sakata K, Hayashi T, Inoue M, Kaneda T, Mabuchi H. Shimizu M, et al. Among authors: sakata k. Am Heart J. 2002 Feb;143(2):289-93. doi: 10.1067/mhj.2002.119760. Am Heart J. 2002. PMID: 11835033

3

Effects of gender on the number of diseased vessels and clinical outcome in Japanese patients with acute coronary syndrome.

Oe K, Shimizu M, Ino H, Yamaguchi M, Terai H, Hayashi K, Kiyama M, Sakata K, Hayashi T, Inoue M, Kaneda T, Mabuchi H. Oe K, et al. Among authors: sakata k. Circ J. 2002 May;66(5):435-40. doi: 10.1253/circj.66.435. Circ J. 2002. PMID: 12030335 Free article.

4

In-hospital outcome in octogenarians with acute coronary syndrome undergoing emergent coronary angiography.

Oe K, Shimizu M, Ino H, Yamaguchi M, Terai H, Hayashi K, Kiyama M, Sakata K, Hayashi T, Inoue M, Kaneda T, Mabuchi H. Oe K, et al. Among authors: sakata k. Jpn Heart J. 2003 Jan;44(1):11-20. doi: 10.1536/jhj.44.11. Jpn Heart J. 2003. PMID: 12622433 Free article.

5

A novel missense mutation in the myosin binding protein-C gene is responsible for hypertrophic cardiomyopathy with left ventricular dysfunction and dilation in elderly patients.

Konno T, Shimizu M, Ino H, Matsuyama T, Yamaguchi M, Terai H, Hayashi K, Mabuchi T, Kiyama M, Sakata K, Hayashi T, Inoue M, Kaneda T, Mabuchi H. Konno T, et al. Among authors: sakata k. J Am Coll Cardiol. 2003 Mar 5;41(5):781-6. doi: 10.1016/s0735-1097(02)02957-1. J Am Coll Cardiol. 2003. PMID: 12628722 Free article.

6

Cardiac sympathetic nerve activity in patients with hypertrophic cardiomyopathy with malignant ventricular tachyarrhythmias.

Terai H, Shimizu M, Ino H, Yamaguchi M, Hayashi K, Sakata K, Kiyama M, Hayashi T, Inoue M, Taki J, Mabuchi H. Terai H, et al. Among authors: sakata k. J Nucl Cardiol. 2003 May-Jun;10(3):304-10. doi: 10.1016/s1071-3581(03)00362-3. J Nucl Cardiol. 2003. PMID: 12794630

7

Q-T peak dispersion in congenital long QT syndrome: possible marker of mutation of HERG.

Inoue M, Shimizu M, Ino H, Yamaguchi M, Terai H, Hayashi K, Kiyama M, Sakata K, Hayashi T, Mabuchi H. Inoue M, et al. Among authors: sakata k. Circ J. 2003 Jun;67(6):495-8. doi: 10.1253/circj.67.495. Circ J. 2003. PMID: 12808265 Free article.

8

Differentiation between patients with takotsubo cardiomyopathy and those with anterior acute myocardial infarction.

Inoue M, Shimizu M, Ino H, Yamaguchi M, Terai H, Fujino N, Sakata K, Funada A, Tatami R, Ishise S, Kanaya H, Mabuchi H. Inoue M, et al. Among authors: sakata k. Circ J. 2005 Jan;69(1):89-94. doi: 10.1253/circj.69.89. Circ J. 2005. PMID: 15635210 Free article.

9

High incidence of sudden cardiac death with conduction disturbances and atrial cardiomyopathy caused by a nonsense mutation in the STA gene.

Sakata K, Shimizu M, Ino H, Yamaguchi M, Terai H, Fujino N, Hayashi K, Kaneda T, Inoue M, Oda Y, Fujita T, Kaku B, Kanaya H, Mabuchi H. Sakata K, et al. Circulation. 2005 Jun 28;111(25):3352-8. doi: 10.1161/CIRCULATIONAHA.104.527184. Epub 2005 Jun 20. Circulation. 2005. PMID: 15967842

10

Abnormal sympathetic innervation of the heart in a patient with Emery-Dreifuss muscular dystrophy.

Fujiita T, Shimizu M, Kaku B, Kanaya H, Horita Y, Uno Y, Yamazaki T, Ohka T, Sakata K, Mabuchi H. Fujiita T, et al. Among authors: sakata k. Ann Nucl Med. 2005 Jul;19(5):411-4. doi: 10.1007/BF03027407. Ann Nucl Med. 2005. PMID: 16164199

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