Uchiyama K - Search Results

1

Differences in diagnostic value of four electrocardiographic voltage criteria for hypertrophic cardiomyopathy in a genotyped population.

Konno T, Shimizu M, Ino H, Fujino N, Hayashi K, Uchiyama K, Kaneda T, Inoue M, Fujita T, Masuta E, Funada A, Mabuchi H. Konno T, et al. Among authors: uchiyama k. Am J Cardiol. 2005 Nov 1;96(9):1308-12. doi: 10.1016/j.amjcard.2005.06.078. Epub 2005 Sep 15. Am J Cardiol. 2005. PMID: 16253604

2

T wave peak-to-end interval and QT dispersion in acquired long QT syndrome: a new index for arrhythmogenicity.

Yamaguchi M, Shimizu M, Ino H, Terai H, Uchiyama K, Oe K, Mabuchi T, Konno T, Kaneda T, Mabuchi H. Yamaguchi M, et al. Among authors: uchiyama k. Clin Sci (Lond). 2003 Dec;105(6):671-6. doi: 10.1042/CS20030010. Clin Sci (Lond). 2003. PMID: 12857349

3

Changes in cardiac sympathetic nerve innervation and activity in pathophysiologic transition from typical to end-stage hypertrophic cardiomyopathy.

Terai H, Shimizu M, Ino H, Yamaguchi M, Uchiyama K, Oe K, Nakajima K, Taki J, Kawano M, Mabuchi H. Terai H, et al. Among authors: uchiyama k. J Nucl Med. 2003 Oct;44(10):1612-7. J Nucl Med. 2003. PMID: 14530475 Free article. Clinical Trial.

4

Autopsy findings in siblings with hypertrophic cardiomyopathy caused by Arg92Trp mutation in the cardiac troponin T gene showing dilated cardiomyopathy-like features.

Shimizu M, Ino H, Yamaguchi M, Terai H, Uchiyama K, Inoue M, Ikeda M, Kawashima A, Mabuchi H. Shimizu M, et al. Among authors: uchiyama k. Clin Cardiol. 2003 Nov;26(11):536-9. doi: 10.1002/clc.4960261112. Clin Cardiol. 2003. PMID: 14640471 Free PMC article.

5

Diagnostic value of abnormal Q waves for identification of preclinical carriers of hypertrophic cardiomyopathy based on a molecular genetic diagnosis.

Konno T, Shimizu M, Ino H, Yamaguchi M, Terai H, Uchiyama K, Oe K, Mabuchi T, Kaneda T, Mabuchi H. Konno T, et al. Among authors: uchiyama k. Eur Heart J. 2004 Feb;25(3):246-51. doi: 10.1016/j.ehj.2003.10.031. Eur Heart J. 2004. PMID: 14972426

6

Gene mutations in adult Japanese patients with dilated cardiomyopathy.

Shimizu M, Ino H, Yasuda T, Fujino N, Uchiyama K, Mabuchi T, Konno T, Kaneda T, Fujita T, Masuta E, Katoh M, Funada A, Mabuchi H. Shimizu M, et al. Among authors: uchiyama k. Circ J. 2005 Feb;69(2):150-3. doi: 10.1253/circj.69.150. Circ J. 2005. PMID: 15671604 Free article.

7

Images in cardiovascular medicine. Adult patient with isolated noncompaction of ventricular myocardium.

Kaneda T, Shimizu M, Ino H, Terai H, Fujino N, Uchiyama K, Mabuchi T, Konno T, Fujita T, Masuda E, Kato H, Funada A, Mabuchi H, Ikeda H. Kaneda T, et al. Among authors: uchiyama k. Circulation. 2005 Aug 16;112(7):e96-7. doi: 10.1161/CIRCULATIONAHA.104.500256. Circulation. 2005. PMID: 16103247 No abstract available.

8

Scintigraphic evaluation of regression of abnormal Q waves in myocardial infarction.

Konno T, Shimizu M, Ino H, Yamaguchi M, Terai H, Uchiyama K, Oe K, Mabuchi T, Kaneda T, Mabuchi H. Konno T, et al. Among authors: uchiyama k. Ann Nucl Med. 2005 Jul;19(5):407-9. doi: 10.1007/BF03027406. Ann Nucl Med. 2005. PMID: 16164198

9

A novel mutation in the cardiac myosin-binding protein C gene is responsible for hypertrophic cardiomyopathy with severe ventricular hypertrophy and sudden death.

Konno T, Shimizu M, Ino H, Fujino N, Uchiyama K, Mabuchi T, Sakata K, Kaneda T, Fujita T, Masuta E, Mabuchi H. Konno T, et al. Among authors: uchiyama k. Clin Sci (Lond). 2006 Jan;110(1):125-31. doi: 10.1042/CS20050189. Clin Sci (Lond). 2006. PMID: 16181148

10

Analysis of ankyrin-B gene mutations in patients with long QT syndrome.

Zhou X, Shimizu M, Konno T, Ino H, Fujino N, Uchiyama K, Mabuchi T, Kaneda T, Fujita T, Masuda E, Kato H, Funada A, Mabuchi H. Zhou X, et al. Among authors: uchiyama k. Nan Fang Yi Ke Da Xue Xue Bao. 2006 Jul;26(7):901-3, 909. Nan Fang Yi Ke Da Xue Xue Bao. 2006. PMID: 16864073

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