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Impact of being large-for-gestational-age on neonatal mortality and morbidities in extremely premature infants

Pediatric research, 2021-10, Vol.90 (4), p.910-916

2021

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Differential Diagnosis Between Catecholaminergic Polymorphic Ventricular Tachycardia and Long QT Syndrome Type 1　― Modified Schwartz Score

Circulation Journal, 2018/08/24, Vol.82(9), pp.2269-2276

2018

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An NGS-based genotyping in LQTS; minor genes are no longer minor

Journal of human genetics, 2020-12, Vol.65 (12), p.1083-1091

2020

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Increased expression of heme oxygenase-1 suppresses airway branching morphogenesis in fetal mouse lungs exposed to inflammation

Pediatric research, 2020-02, Vol.87 (3), p.494-500

2020

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Dynamic QT Changes in Long QT Syndrome Type 8

Circulation Journal, 2019/06/25, Vol.83(7), pp.1614

2019

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High Prevalence of Late-Appearing T-Wave in Patients With Long QT Syndrome Type 8

Circulation Journal, 2020/03/25, Vol.84(4), pp.559-568

2020

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Novel electrocardiographic criteria for short QT syndrome in children and adolescents

Europace (London, England), 2021-12, Vol.23 (12), p.2029-2038

2021

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Therapeutic response of iNO in preterm infants with hypoxemic respiratory failure

Pediatrics international, 2023-01, Vol.65 (1), p.e15423-n/a

2023

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Increased CaV1.2 late current by a CACNA1C p.R412M variant causes an atypical Timothy syndrome without syndactyly

Scientific reports, 2022-11, Vol.12 (1), p.18984-18984, Article 18984

2022

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Difference in pyruvic acid metabolism between neonatal and adult mouse lungs exposed to hyperoxia

PloS one, 2020-09, Vol.15 (9), p.e0238604-e0238604

2020

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Copy number variations of SCN5A in Brugada syndrome

Heart rhythm, 2018-08, Vol.15 (8), p.1179-1188

2018

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School-based routine screenings of electrocardiograms for the diagnosis of long QT syndrome

Europace (London, England), 2022-10, Vol.24 (9), p.1496-1503

2022

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A severe case of cardiospondylocarpofacial syndrome with a novel MAP3K7 variant

Human genome variation, 2024-02, Vol.11 (1), p.8-8, Article 8

2024

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Efficacy of cEEG and hepatic function to diagnose early acute encephalopathy

Pediatrics international, 2023-01, Vol.65 (1), p.e15494-n/a

2023

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Preterm Infant with Generalized Arterial Calcification of Infancy Who Survived Due to Early Diagnosis and Appropriate Treatment with Bisphosphonates: A Case Report

Children (Basel), 2024-09, Vol.11 (10), p.1176

2024

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Phenotypic Variability of ANK2 Mutations in Patients With Inherited Primary Arrhythmia Syndromes

Circulation Journal, 2016/11/25, Vol.80(12), pp.2435-2442

2016

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Cytomegalovirus‐related sepsis‐like syndrome in very premature infants in Japan

Pediatrics international, 2022-01, Vol.64 (1), p.e14994-n/a

2022

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Pediatric Cohort With Long QT Syndrome　– KCNH2 Mutation Carriers Present Late Onset But Severe Symptoms

Circulation Journal, 2016/02/25, Vol.80(3), pp.696-702

2016

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Thioredoxin-1 Ameliorates Oxygen-Induced Retinopathy in Newborn Mice through Modulation of Proinflammatory and Angiogenic Factors

Antioxidants, 2022-04, Vol.11 (5), p.899

2022

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Short QT syndrome in a boy diagnosed on screening for heart disease

Pediatrics international, 2014-10, Vol.56 (5), p.774-776

2014

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Multigenerational Inheritance of Long QT Syndrome Type 2 in a Japanese Family

Internal Medicine, 2016, Vol.55(3), pp.259-262

2016

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Attenuation of Hyperoxic Lung Injury in Newborn Thioredoxin-1-Overexpressing Mice through the Suppression of Proinflammatory Cytokine mRNA Expression

Biomedicines, 2020-03, Vol.8 (3), p.66

2020

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Microforce Material Tester Using Small Pendulum II

Key engineering materials, 2012-01, Vol.497, p.169-175

2012

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The serum thioredoxin-1 levels are not associated with bronchopulmonary dysplasia and retinopathy of prematurity

Pediatric research, 2024-02, Vol.96 (5), p.1275-1282

2024

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Impact of being large-for-gestational-age on neonatal mortality and morbidities in extremely premature infants

Differential Diagnosis Between Catecholaminergic Polymorphic Ventricular Tachycardia and Long QT Syndrome Type 1　― Modified Schwartz Score

An NGS-based genotyping in LQTS; minor genes are no longer minor

Increased expression of heme oxygenase-1 suppresses airway branching morphogenesis in fetal mouse lungs exposed to inflammation

Dynamic QT Changes in Long QT Syndrome Type 8

High Prevalence of Late-Appearing T-Wave in Patients With Long QT Syndrome Type 8

Novel electrocardiographic criteria for short QT syndrome in children and adolescents

Therapeutic response of iNO in preterm infants with hypoxemic respiratory failure

Increased CaV1.2 late current by a CACNA1C p.R412M variant causes an atypical Timothy syndrome without syndactyly

Difference in pyruvic acid metabolism between neonatal and adult mouse lungs exposed to hyperoxia

Copy number variations of SCN5A in Brugada syndrome

School-based routine screenings of electrocardiograms for the diagnosis of long QT syndrome

A severe case of cardiospondylocarpofacial syndrome with a novel MAP3K7 variant

Efficacy of cEEG and hepatic function to diagnose early acute encephalopathy

Preterm Infant with Generalized Arterial Calcification of Infancy Who Survived Due to Early Diagnosis and Appropriate Treatment with Bisphosphonates: A Case Report

Phenotypic Variability of ANK2 Mutations in Patients With Inherited Primary Arrhythmia Syndromes

Cytomegalovirus‐related sepsis‐like syndrome in very premature infants in Japan

Pediatric Cohort With Long QT Syndrome　– KCNH2 Mutation Carriers Present Late Onset But Severe Symptoms

Contribution of a KCNH2 variant in genotyped long QT syndrome: Romano–Ward syndrome under double mutations and acquired long QT syndrome under heterozygote

Thioredoxin-1 Ameliorates Oxygen-Induced Retinopathy in Newborn Mice through Modulation of Proinflammatory and Angiogenic Factors

Short QT syndrome in a boy diagnosed on screening for heart disease

Multigenerational Inheritance of Long QT Syndrome Type 2 in a Japanese Family

Attenuation of Hyperoxic Lung Injury in Newborn Thioredoxin-1-Overexpressing Mice through the Suppression of Proinflammatory Cytokine mRNA Expression

Microforce Material Tester Using Small Pendulum II

The serum thioredoxin-1 levels are not associated with bronchopulmonary dysplasia and retinopathy of prematurity

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