T. Fujita

发表

High Incidence of Sudden Cardiac Death With Conduction Disturbances and Atrial Cardiomyopathy Caused by a Nonsense Mutation in the STA Gene

K. Hayashi, H. Mabuchi, M. Yamaguchi, 2005, Circulation.

Gene mutations in adult Japanese patients with dilated cardiomyopathy.

H. Mabuchi, M. Shimizu, H. Ino, 2005, Circulation journal : official journal of the Japanese Circulation Society.

Characterization of baseline clinical factors associated with incident worsening kidney function in patients with non-valvular atrial fibrillation: the Hokuriku-Plus AF Registry

R. Passman, M. Yamagishi, K. Mori, 2022, Heart and Vessels.

Fragmented QRS predicts heart failure progression in patients with hypertrophic cardiomyopathy.

K. Hayashi, M. Yamagishi, M. Kawashiri, 2014, Circulation journal : official journal of the Japanese Circulation Society.

J Waves for Predicting Cardiac Events in Hypertrophic Cardiomyopathy.

K. Hayashi, M. Yamagishi, M. Kawashiri, 2017, JACC. Clinical electrophysiology.

Compound heterozygosity deteriorates phenotypes of hypertrophic cardiomyopathy with founder MYBPC3 mutation: evidence from patients and zebrafish models.

K. Hayashi, M. Yamagishi, M. Kawashiri, 2014, American journal of physiology. Heart and circulatory physiology.

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

Xiaoping Zhou, H. Mabuchi, M. Shimizu, 2006, Nan fang yi ke da xue xue bao = Journal of Southern Medical University.

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

H. Mabuchi, M. Shimizu, H. Ino, 2006, Clinical science.

Attitudes to bystander cardiopulmonary resuscitation in Japan in 2010.

M. Takamura, M. Okajima, T. Taniguchi, 2012, Circulation journal : official journal of the Japanese Circulation Society.

Increased extent of myocardial fibrosis in genotyped hypertrophic cardiomyopathy with ventricular tachyarrhythmias.

K. Hayashi, M. Yamagishi, M. Kawashiri, 2015, Journal of cardiology.

Sarcomere gene mutations are associated with increased cardiovascular events in left ventricular hypertrophy: results from multicenter registration in Japan.

I. Komuro, M. Yano, Shigeki Kobayashi, 2013, JACC. Heart failure.

Impact of Systolic Dysfunction in Genotyped Hypertrophic Cardiomyopathy

K. Hayashi, M. Yamagishi, M. Kawashiri, 2013, Clinical cardiology.

Impact of functional studies on exome sequence variant interpretation in early-onset cardiac conduction system diseases.

Yanbin Zhao, M. Yamagishi, Micah L. Burch, 2020, Cardiovascular research.

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

H. Mabuchi, M. Shimizu, K. Sakata, 2005, Annals of nuclear medicine.

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

H. Ikeda, H. Mabuchi, M. Shimizu, 2005, Circulation.

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

K. Hayashi, H. Mabuchi, M. Shimizu, 2005, The American journal of cardiology.

Abstract 17669: Compound heterozygosity of Cardiac Myosin Biding Protein C Gene Mutation Worsens Clinical Outcome of Hypertrophic Cardiomyopathy: Evidence from Comparison with Simple Founder Mutation Carriers

K. Hayashi, M. Yamagishi, T. Konno, 2012 .

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

H. Ikeda, H. Mabuchi, M. Shimizu, 2005, Circulation.