Anan R - Search Results

1

A novel deletion mutation in the cardiac myosin-binding protein C gene as a cause of Maron's type IV hypertrophic cardiomyopathy.

Anan R, Niimura H, Minagoe S, Tei C. Anan R, et al. Am J Cardiol. 2002 Feb 15;89(4):487-8. doi: 10.1016/s0002-9149(01)02281-0. Am J Cardiol. 2002. PMID: 11835941 No abstract available.

2

Mutations in the genes for sarcomeric proteins in Japanese patients with onset sporadic hypertrophic cardiomyopathy after age 40 years.

Anan R, Niimura H, Takenaka T, Hamasaki S, Tei C. Anan R, et al. Am J Cardiol. 2007 Jun 15;99(12):1750-4. doi: 10.1016/j.amjcard.2007.01.066. Epub 2007 Apr 26. Am J Cardiol. 2007. PMID: 17560888

3

Prevalence and time of appearance of Brugada electrocardiographic pattern in young male adolescents from a three-year follow-up study.

Yoshinaga M, Anan R, Nomura Y, Tanaka Y, Tanaka Y, Sarantuya J, Oku S, Nishi S, Kawano Y, Tei C, Arima K. Yoshinaga M, et al. Among authors: anan r. Am J Cardiol. 2004 Nov 1;94(9):1186-9. doi: 10.1016/j.amjcard.2004.07.092. Am J Cardiol. 2004. PMID: 15518619

4

Limitation of angiography to identify the culprit plaque in acute myocardial infarction with coronary total occlusion utility of coronary plaque temperature measurement to identify the culprit plaque.

Takumi T, Lee S, Hamasaki S, Toyonaga K, Kanda D, Kusumoto K, Toda H, Takenaka T, Miyata M, Anan R, Otsuji Y, Tei C. Takumi T, et al. Among authors: anan r. J Am Coll Cardiol. 2007 Dec 4;50(23):2197-203. doi: 10.1016/j.jacc.2007.07.079. Epub 2007 Nov 19. J Am Coll Cardiol. 2007. PMID: 18061065 Free article. Clinical Trial.

5

Terminal stage cardiac findings in patients with cardiac Fabry disease: an electrocardiographic, echocardiographic, and autopsy study.

Takenaka T, Teraguchi H, Yoshida A, Taguchi S, Ninomiya K, Umekita Y, Yoshida H, Horinouchi M, Tabata K, Yonezawa S, Yoshimitsu M, Higuchi K, Nakao S, Anan R, Minagoe S, Tei C. Takenaka T, et al. Among authors: anan r. J Cardiol. 2008 Feb;51(1):50-9. doi: 10.1016/j.jjcc.2007.12.001. Epub 2008 Feb 6. J Cardiol. 2008. PMID: 18522775 Free article.

6

Novel cardiac beta-myosin heavy chain gene missense mutations (R869C and R870C) that cause familial hypertrophic cardiomyopathy.

Anan R, Shono H, Tei C. Anan R, et al. Hum Mutat. 2000 Jun;15(6):584. doi: 10.1002/1098-1004(200006)15:6<584::AID-HUMU25>3.0.CO;2-R. Hum Mutat. 2000. PMID: 10862102 No abstract available.

7

[Genotype-phenotype correlations in familial hypertrophic cardiomyopathy].

Anan R, Niimura H, Tei C. Anan R, et al. Nihon Rinsho. 2000 Jan;58(1):134-40. Nihon Rinsho. 2000. PMID: 10885301 Review. Japanese.

8

Epsilon waves in a patient with arrhythmogenic right ventricular cardiomyopathy.

Anan R, Takenaka T, Tei C. Anan R, et al. Heart. 2002 Nov;88(5):444. doi: 10.1136/heart.88.5.444-a. Heart. 2002. PMID: 12381622 Free PMC article. No abstract available.

9

Intracardiac thrombus, superior vena cava syndrome, and pulmonary embolism in a patient with Behçet's disease: a case report and literature review.

Kajiya T, Anan R, Kameko M, Mizukami N, Minagoe S, Hamasaki S, Maruyama I, Sakata R, Tei C. Kajiya T, et al. Among authors: anan r. Heart Vessels. 2007 Jul;22(4):278-83. doi: 10.1007/s00380-006-0973-6. Epub 2007 Jul 20. Heart Vessels. 2007. PMID: 17653524 Review.

10

Usefulness and cost effectiveness of cardiovascular screening of young adolescents.

Tanaka Y, Yoshinaga M, Anan R, Tanaka Y, Nomura Y, Oku S, Nishi S, Kawano Y, Tei C, Arima K. Tanaka Y, et al. Among authors: anan r. Med Sci Sports Exerc. 2006 Jan;38(1):2-6. doi: 10.1249/01.mss.0000183187.88000.53. Med Sci Sports Exerc. 2006. PMID: 16394946

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