Fujino N - Search Results

1

Personalized medicine for cardiovascular diseases.

Tada H, Fujino N, Nomura A, Nakanishi C, Hayashi K, Takamura M, Kawashiri MA. Tada H, et al. Among authors: fujino n. J Hum Genet. 2021 Jan;66(1):67-74. doi: 10.1038/s10038-020-0818-7. Epub 2020 Aug 8. J Hum Genet. 2021. PMID: 32772049 Review.

2

[Monitoring, examination, special equipment, handling of drugs and the keypoints in neonatal emergencies].

Fujino N, Tada H. Fujino N, et al. Josanpu Zasshi. 1981 Apr;35(4):271-7. Josanpu Zasshi. 1981. PMID: 6911165 Japanese. No abstract available.

3

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. Among authors: fujino n. Circulation. 2005 Jun 28;111(25):3352-8. doi: 10.1161/CIRCULATIONAHA.104.527184. Epub 2005 Jun 20. Circulation. 2005. PMID: 15967842

4

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: fujino n. 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

5

Differences in the diagnostic value of various criteria of negative T waves for hypertrophic cardiomyopathy based on a molecular genetic diagnosis.

Konno T, Fujino N, Hayashi K, Uchiyama K, Masuta E, Katoh H, Sakamoto Y, Tsubokawa T, Ino H, Yamagishi M. Konno T, et al. Among authors: fujino n. Clin Sci (Lond). 2007 Jun;112(11):577-82. doi: 10.1042/CS20060293. Clin Sci (Lond). 2007. PMID: 17263690

6

[Restrictive cardiomyopathy associated with heart failure].

Konno T, Ino H, Fujino N, Hayashi K, Yamagishi M. Konno T, et al. Among authors: fujino n. Nihon Rinsho. 2007 May 28;65 Suppl 5:430-7. Nihon Rinsho. 2007. PMID: 17571415 Review. Japanese. No abstract available.

7

Expression and function of ephrin-B1 and its cognate receptor EphB2 in human atherosclerosis: from an aspect of chemotaxis.

Sakamoto A, Ishibashi-Ueda H, Sugamoto Y, Higashikata T, Miyamoto S, Kawashiri MA, Yagi K, Konno T, Hayashi K, Fujino N, Ino H, Takeda Y, Yamagishi M. Sakamoto A, et al. Among authors: fujino n. Clin Sci (Lond). 2008 May;114(10):643-50. doi: 10.1042/CS20070339. Clin Sci (Lond). 2008. PMID: 18092944

8

Assessment of QT intervals and prevalence of short QT syndrome in Japan.

Funada A, Hayashi K, Ino H, Fujino N, Uchiyama K, Sakata K, Masuta E, Sakamoto Y, Tsubokawa T, Yamagishi M. Funada A, et al. Among authors: fujino n. Clin Cardiol. 2008 Jun;31(6):270-4. doi: 10.1002/clc.20208. Clin Cardiol. 2008. PMID: 18543308 Free PMC article.

9

Impact of QT variables on clinical outcome of genotyped hypertrophic cardiomyopathy.

Uchiyama K, Hayashi K, Fujino N, Konno T, Sakamoto Y, Sakata K, Kawashiri MA, Ino H, Yamagishi M. Uchiyama K, et al. Among authors: fujino n. Ann Noninvasive Electrocardiol. 2009 Jan;14(1):65-71. doi: 10.1111/j.1542-474X.2008.00275.x. Ann Noninvasive Electrocardiol. 2009. PMID: 19149795 Free PMC article.

10

Long QT syndrome and associated gene mutation carriers in Japanese children: results from ECG screening examinations.

Hayashi K, Fujino N, Uchiyama K, Ino H, Sakata K, Konno T, Masuta E, Funada A, Sakamoto Y, Tsubokawa T, Nakashima K, Liu L, Higashida H, Hiramaru Y, Shimizu M, Yamagishi M. Hayashi K, et al. Among authors: fujino n. Clin Sci (Lond). 2009 Sep 21;117(12):415-24. doi: 10.1042/CS20080528. Clin Sci (Lond). 2009. PMID: 19371231

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