Megumi Fukuyama

Long-Term Arrhythmic Outcomes of KCNJ2 Variant Carriers in Japan.

Journal: Circulation. Genomic and precision medicine

Published: September 30, 2025

Congenital Short QT Syndrome　- Review Focused on KCNQ1 p.Val141Met Variant.

Journal: Circulation journal : official journal of the Japanese Circulation Society

Published: May 14, 2025

Long-term follow-up of patients with catecholaminergic polymorphic ventricular tachycardia related to a novel CALM2 variant.

Journal: Journal of cardiology cases

Published: April 03, 2025

Clinical Impact of Genetic Testing for Long QT Syndrome　- Evidence From a Nationwide LQTS Registry in Japan.

Journal: Circulation journal : official journal of the Japanese Circulation Society

Published: March 30, 2025

SCN5A variant type-dependent risk prediction in Brugada syndrome.

Journal: Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology

Published: November 14, 2024

Holter Electrocardiographic Approach to Predicting Outcomes of Pediatric Patients With Long QT Syndrome.

Journal: Circulation journal : official journal of the Japanese Circulation Society

Published: December 03, 2023

Clinical characterization of type 1 long QT syndrome caused by C-terminus Kv7.1 variants.

Journal: Heart rhythm

Published: July 31, 2023

Calmodulinopathy in Japanese Children　- Their Cardiac Phenotypes Are Severe and Show Early Onset in Fetal Life and Infancy.

Journal: Circulation journal : official journal of the Japanese Circulation Society

Published: June 28, 2023

Novel Calmodulin Variant p.E46K Associated With Severe Catecholaminergic Polymorphic Ventricular Tachycardia Produces Robust Arrhythmogenicity in Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes.

Journal: Circulation. Arrhythmia and electrophysiology

Published: March 03, 2023

FFR-CT is extremely useful in detecting hemodynamically significant left-main coronary artery stenosis with right coronary artery hypoplasia: A case report.

Journal: Journal of cardiology cases

Published: February 18, 2023

Clopidogrel Use in CYP2C19 Loss-of-Function Carriers With High Bleeding Risk After Percutaneous Coronary Intervention.

Journal: Circulation journal : official journal of the Japanese Circulation Society

Published: February 15, 2023

Clinical presentation of calmodulin mutations: the International Calmodulinopathy Registry.

Journal: European heart journal

Published: January 18, 2023

Long-Term Arrhythmic Outcomes of KCNJ2 Variant Carriers in Japan.

Long-Term Arrhythmic Outcomes of KCNJ2 Variant Carriers in Japan.

Congenital Short QT Syndrome - Review Focused on KCNQ1 p.Val141Met Variant.

Congenital Short QT Syndrome - Review Focused on KCNQ1 p.Val141Met Variant.

Long-term follow-up of patients with catecholaminergic polymorphic ventricular tachycardia related to a novel CALM2 variant.

Long-term follow-up of patients with catecholaminergic polymorphic ventricular tachycardia related to a novel CALM2 variant.

Clinical Impact of Genetic Testing for Long QT Syndrome - Evidence From a Nationwide LQTS Registry in Japan.

Clinical Impact of Genetic Testing for Long QT Syndrome - Evidence From a Nationwide LQTS Registry in Japan.

SCN5A variant type-dependent risk prediction in Brugada syndrome.

SCN5A variant type-dependent risk prediction in Brugada syndrome.

Holter Electrocardiographic Approach to Predicting Outcomes of Pediatric Patients With Long QT Syndrome.

Holter Electrocardiographic Approach to Predicting Outcomes of Pediatric Patients With Long QT Syndrome.

Clinical characterization of type 1 long QT syndrome caused by C-terminus Kv7.1 variants.

Clinical characterization of type 1 long QT syndrome caused by C-terminus Kv7.1 variants.

Calmodulinopathy in Japanese Children - Their Cardiac Phenotypes Are Severe and Show Early Onset in Fetal Life and Infancy.

Calmodulinopathy in Japanese Children - Their Cardiac Phenotypes Are Severe and Show Early Onset in Fetal Life and Infancy.

Novel Calmodulin Variant p.E46K Associated With Severe Catecholaminergic Polymorphic Ventricular Tachycardia Produces Robust Arrhythmogenicity in Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes.

Novel Calmodulin Variant p.E46K Associated With Severe Catecholaminergic Polymorphic Ventricular Tachycardia Produces Robust Arrhythmogenicity in Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes.

FFR-CT is extremely useful in detecting hemodynamically significant left-main coronary artery stenosis with right coronary artery hypoplasia: A case report.

FFR-CT is extremely useful in detecting hemodynamically significant left-main coronary artery stenosis with right coronary artery hypoplasia: A case report.

Clopidogrel Use in CYP2C19 Loss-of-Function Carriers With High Bleeding Risk After Percutaneous Coronary Intervention.

Clopidogrel Use in CYP2C19 Loss-of-Function Carriers With High Bleeding Risk After Percutaneous Coronary Intervention.

Clinical presentation of calmodulin mutations: the International Calmodulinopathy Registry.

Clinical presentation of calmodulin mutations: the International Calmodulinopathy Registry.

Congenital Short QT Syndrome　- Review Focused on KCNQ1 p.Val141Met Variant.

Congenital Short QT Syndrome　- Review Focused on KCNQ1 p.Val141Met Variant.

Clinical Impact of Genetic Testing for Long QT Syndrome　- Evidence From a Nationwide LQTS Registry in Japan.

Clinical Impact of Genetic Testing for Long QT Syndrome　- Evidence From a Nationwide LQTS Registry in Japan.

Calmodulinopathy in Japanese Children　- Their Cardiac Phenotypes Are Severe and Show Early Onset in Fetal Life and Infancy.

Calmodulinopathy in Japanese Children　- Their Cardiac Phenotypes Are Severe and Show Early Onset in Fetal Life and Infancy.