Noboru Fujino

[Restrictive cardiomyopathy associated with heart failure].

A novel beta-myosin heavy chain gene mutation, p.Met531Arg, identified in isolated left ventricular non-compaction in humans, results in left ventricular hypertrophy that progresses to dilation in a mouse model.

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

Impact of anti-apoptotic and anti-oxidative effects of bone marrow mesenchymal stem cells with transient overexpression of heme oxygenase-1 on myocardial ischemia.

Heterogeneity of clinical manifestation of hypertrophic cardiomyopathy caused by deletion of lysine 183 in cardiac troponin I gene.

Impact of renin-angiotensin system polymorphisms on development of systolic dysfunction in hypertrophic cardiomyopathy. Evidence from a study of genotyped patients.

Efficacy and safety of coadministration of rosuvastatin, ezetimibe, and colestimide in heterozygous familial hypercholesterolemia.

Impact of systolic dysfunction in genotyped hypertrophic cardiomyopathy.

Current perspectives in genetic cardiovascular disorders: from basic to clinical aspects.

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

Left ventricular apical aneurysm and systolic dysfunction in hypertrophic cardiomyopathy.

High sensitivity of late gadolinium enhancement for predicting microscopic myocardial scarring in biopsied specimens in hypertrophic cardiomyopathy.

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

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

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

Right ventricular hypertrophy is associated with cardiovascular events in hypertrophic cardiomyopathy: evidence from study with magnetic resonance imaging.

Electrocardiographic QRS Fragmentation as a Marker for Myocardial Fibrosis in Hypertrophic Cardiomyopathy.

Functional Characterization of Rare Variants Implicated in Susceptibility to Lone Atrial Fibrillation.

Hypokalemia and the Disappearance of Giant Negative T Waves.

Overview of the 81 Annual Scientific Meeting of the Japanese Circulation Society　- Cardiovascular Medicine for the Next Generation.

Characteristics of induced pluripotent stem cells from clinically divergent female monozygotic twins with Danon disease.

Heat Failure Phenotypes Induced by Knockdown of DAPIT in Zebrafish: A New Insight into Mechanism of Dilated Cardiomyopathy.

Late Gadolinium Enhancement for Prediction of Mutation-Positive Hypertrophic Cardiomyopathy on the Basis of Panel-Wide Sequencing.

Author Correction: Heart Failure Phenotypes Induced by Knockdown of DAPIT in Zebrafish: A New Insight into Mechanism of Dilated Cardiomyopathy.

Impact of Updated Diagnostic Criteria for Long QT Syndrome on Clinical Detection of Diseased Patients: Results From a Study of Patients Carrying Gene Mutations.

Limited effects of long-term enzyme replacement therapy on the cardiac conduction system in Fabry disease.

Impact of inflow reduction of arteriovenous fistula on systemic hemodynamics in a patient with high-output heart failure during hemodialysis: A case report.

Idiopathic dissection from left subclavian artery to brachial artery: Spontaneous repair with conservative management.

Impact of cardiac myosin light chain kinase gene mutation on development of dilated cardiomyopathy.

Impact of renal function on mid-term outcomes in heart failure patients treated with tolvaptan.