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Postmortem Genetic Analysis Of Sudden Unexplained Death Syndrome Under 50 Years Of Age: A Next-Generation Sequencing Study

Heart rhythm, 2016-07, Vol.13 (7), p.1544-1551

2016

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A Novel NKX2-5 Variant in a Child with Left Ventricular Noncompaction, Atrial Septal Defect, Atrioventricular Conduction Disorder, and Syncope

Journal of clinical medicine, 2022-06, Vol.11 (11), p.3171

2022

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TBX5 R264K acts as a modifier to develop dilated cardiomyopathy in mice independently of T-box pathway

PloS one, 2020-04, Vol.15 (4), p.e0227393-e0227393

2020

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Lack of modulatory effect of the SCN5A R1193Q polymorphism on cardiac fast Na+ current at body temperature

PloS one, 2018-11, Vol.13 (11), p.e0207437-e0207437

2018

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Intramyocardial bronchogenic cyst: histological appearance and a review of the literature

Cardiovascular pathology, 2017-05, Vol.28, p.64-67

2017

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Sudden unexpected death with primary adrenal lymphoma

Legal medicine (Tokyo, Japan), 2018-11, Vol.35, p.25-28

2018

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Novel MYH7 Variant in the Neonate of a Mother with Gestational Diabetes Mellitus Showing Left Ventricular Hypertrophy and Noncompaction

Genes, 2024-03, Vol.15 (3), p.381

2024

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Clinical and Echocardiographic Impact of Tafazzin Variants on Dilated Cardiomyopathy Phenotype in Left Ventricular Non-Compaction Patients in Early Infancy

Circulation Journal, 2018/09/25, Vol.82(10), pp.2609-2618

2018

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An Autopsy Case of Sudden Unexpected Death of a Young Adult in a Hot Bath: Molecular Analysis Using Next-Generation DNA Sequencing

Clinical medicine insights. Case reports, 2017, Vol.2017 (10), p.1179547617702884

2017

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Nitrative Stress and Tau Accumulation in Amyotrophic Lateral Sclerosis/Parkinsonism-Dementia Complex (ALS/PDC) in the Kii Peninsula, Japan

Frontiers in neuroscience, 2018-01, Vol.11, p.751-751

2018

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Pseudoaneurysmal defect of mitral-aortic intervalvular fibrosa is likely to be a cerebral embolic source. An autopsy study in remote period from the stroke

Pathology international, 2016-08, Vol.66 (8), p.472-474

2016

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Low-frequency maternal novel MYH7 mosaicism mutation in recurrent fetal-onset severe left ventricular noncompaction: a case report

Frontiers in pediatrics, 2023-06, Vol.11, p.1195222

2023

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Tachycardia-Induced Cardiomyopathy in an Infant with Atrial Flutter and Prolonged Recovery of Cardiac Function

Journal of clinical medicine, 2024-06, Vol.13 (11), p.3313

2024

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A double heterozygous variant in MYH6 and MYH7 associated with hypertrophic cardiomyopathy in a Japanese Family

Journal of cardiology cases, 2022-04, Vol.25 (4), p.213-217

2022

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Left Ventricular Noncompaction and Congenital Heart Disease Increases the Risk of Congestive Heart Failure

Journal of clinical medicine, 2020-03, Vol.9 (3), p.785

2020

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Clinicopathological and Genetic Profiles of Cases with Myocyte Disarray—Investigation for Establishing the Autopsy Diagnostic Criteria for Hypertrophic Cardiomyopathy

Journal of clinical medicine, 2019-04, Vol.8 (4), p.463

2019

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Latent pathogenicity of the G38S polymorphism of KCNE1 K+ channel modulator

Heart and vessels, 2017-02, Vol.32 (2), p.186-192

2017

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A mutant HCN4 channel in a family with bradycardia, left bundle branch block, and left ventricular noncompaction

Heart and vessels, 2018-07, Vol.33 (7), p.802-819

2018

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The Susceptibilities of Human Ether-à-Go-Go-Related Gene Channel with the G487R Mutation to Arrhythmogenic Factors

Biological and Pharmaceutical Bulletin, 2015/05/01, Vol.38(5), pp.781-784

2015

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A Case Report of a Rare Heterozygous Variant in the Desmin Gene Associated With Hypertrophic Cardiomyopathy and Complete Atrioventricular Block

CJC open (Online), 2021-09, Vol.3 (9), p.1195-1198

2021

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Anomalous origin of the right coronary artery evaluated with multidetector computed tomography and its clinical relevance

Journal of cardiology, 2016-09, Vol.68 (3), p.196-201

2016

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High takeoff of the left main coronary artery at autopsy after sudden unexpected death in a male

Pathology, 2014-06, Vol.46 (4), p.361-364

2014

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Modification of KCNH2-Encoded Cardiac Potassium Channels by KCNE1 Polymorphism: Reply

Circulation Journal, 2014/08/25, Vol.78(9), pp.2331

2014

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Glycine/Serine Polymorphism at Position 38 Influences KCNE1 Subunit’s Modulatory Actions on Rapid and Slow Delayed Rectifier K+ Currents

Circulation Journal, 2014, Vol.78(3), pp.610-618

2014

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The Susceptibilities of Human Ether-a-Go-Go-Related Gene Channel with the G487R Mutation to Arrhythmogenic Factors

Biological and Pharmaceutical Bulletin, 2015-05, Vol.38 (5), p.781-784

2015

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Postmortem Genetic Analysis Of Sudden Unexplained Death Syndrome Under 50 Years Of Age: A Next-Generation Sequencing Study

A Novel NKX2-5 Variant in a Child with Left Ventricular Noncompaction, Atrial Septal Defect, Atrioventricular Conduction Disorder, and Syncope

TBX5 R264K acts as a modifier to develop dilated cardiomyopathy in mice independently of T-box pathway

Lack of modulatory effect of the SCN5A R1193Q polymorphism on cardiac fast Na+ current at body temperature

Intramyocardial bronchogenic cyst: histological appearance and a review of the literature

Sudden unexpected death with primary adrenal lymphoma

Novel MYH7 Variant in the Neonate of a Mother with Gestational Diabetes Mellitus Showing Left Ventricular Hypertrophy and Noncompaction

Clinical and Echocardiographic Impact of Tafazzin Variants on Dilated Cardiomyopathy Phenotype in Left Ventricular Non-Compaction Patients in Early Infancy

An Autopsy Case of Sudden Unexpected Death of a Young Adult in a Hot Bath: Molecular Analysis Using Next-Generation DNA Sequencing

Nitrative Stress and Tau Accumulation in Amyotrophic Lateral Sclerosis/Parkinsonism-Dementia Complex (ALS/PDC) in the Kii Peninsula, Japan

Pseudoaneurysmal defect of mitral-aortic intervalvular fibrosa is likely to be a cerebral embolic source. An autopsy study in remote period from the stroke

Low-frequency maternal novel MYH7 mosaicism mutation in recurrent fetal-onset severe left ventricular noncompaction: a case report

Tachycardia-Induced Cardiomyopathy in an Infant with Atrial Flutter and Prolonged Recovery of Cardiac Function

A double heterozygous variant in MYH6 and MYH7 associated with hypertrophic cardiomyopathy in a Japanese Family

Left Ventricular Noncompaction and Congenital Heart Disease Increases the Risk of Congestive Heart Failure

Clinicopathological and Genetic Profiles of Cases with Myocyte Disarray—Investigation for Establishing the Autopsy Diagnostic Criteria for Hypertrophic Cardiomyopathy

Latent pathogenicity of the G38S polymorphism of KCNE1 K+ channel modulator

A mutant HCN4 channel in a family with bradycardia, left bundle branch block, and left ventricular noncompaction

The Susceptibilities of Human Ether-à-Go-Go-Related Gene Channel with the G487R Mutation to Arrhythmogenic Factors

A Case Report of a Rare Heterozygous Variant in the Desmin Gene Associated With Hypertrophic Cardiomyopathy and Complete Atrioventricular Block

Anomalous origin of the right coronary artery evaluated with multidetector computed tomography and its clinical relevance

High takeoff of the left main coronary artery at autopsy after sudden unexpected death in a male

Modification of KCNH2-Encoded Cardiac Potassium Channels by KCNE1 Polymorphism: Reply

Glycine/Serine Polymorphism at Position 38 Influences KCNE1 Subunit’s Modulatory Actions on Rapid and Slow Delayed Rectifier K+ Currents

The Susceptibilities of Human Ether-a-Go-Go-Related Gene Channel with the G487R Mutation to Arrhythmogenic Factors

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