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Caffeine Intoxication in Pregnancy: Report of a case

Archives of academic emergency medicine, 2019-11, Vol.7 (1)

2019

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Emphysematous cystitis successfully treated with hyperbaric oxygen therapy: case report

Undersea & hyperbaric medicine, 2018-11, Vol.45 (6), p.701-703

2018

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Successful Cardiac, Lung, and Kidney Transplantation from a Methanol-poisoned Donor

JMA journal, 2024, Vol.7 (1), p.133-135

2024

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Successfully treated case of severe hypothermia secondary to myxedema coma

Acute medicine & surgery, 2023, Vol.10 (1), p.e828-e828

2023

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Epileptic Seizure from Ginkgo Nut Intoxication in an Adult

Case reports in emergency medicine, 2020, Vol.2020, p.5072954-5072954

2020

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Extracorporeal cardiopulmonary resuscitation in out-of-hospital cardiac arrest patients by cannulating the right internal jugular vein for outflow

Nihon Shūchū Chiryō Igakkai zasshi, 2017-03, Vol.24 (2), p.131-135

2017

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Caffeine Intoxication in Pregnancy; a case Report

Archives of academic emergency medicine, 2019, Vol.7 (1), p.e67-e67

2019

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Ictal Cardiorespiratory Arrest Associated with Status Epilepticus in Panayiotopoulos Syndrome

Acta medica Okayama, 2018, Vol.72 (3), p.297-300

2018

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Blended phenotype of AP4E1 deficiency and Angelman syndrome caused by paternal isodisomy of chromosome 15

Brain & development (Tokyo. 1979), 2020-03, Vol.42 (3), p.289-292

2020

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Omega-3 fatty acid epoxides produced by PAF-AH2 in mast cells regulate pulmonary vascular remodeling

Nature communications, 2022-05, Vol.13 (1), p.3013-3013, Article 3013

2022

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Extracorporeal cardiopulmonary resuscitation in adult patients with out-of-hospital cardiac arrest: a retrospective large cohort multicenter study in Japan

Critical care (London, England), 2022-05, Vol.26 (1), p.129-129, Article 129

2022

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Peripheral pulmonary stenosis with Noonan syndrome treated by balloon pulmonary angioplasty

Pulmonary circulation, 2020-10, Vol.10 (4), p.1-3

2020

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TNFRSF13B c.226G>A (p.Gly76Ser) as a Novel Causative Mutation for Pulmonary Arterial Hypertension

Journal of the American Heart Association, 2021-02, Vol.10 (5), p.e019245

2021

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Bulk and surface uniformity of magnetic and electronic structures in epitaxial W / Mn 3 Sn / MgO films revealed by fluorescence- and electron-yield x-ray magnetic circular dichroism

Physical review. B, 2024-08, Vol.110 (6), Article L060412

2024

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Mexiletine shortens the QT interval in a pedigree of KCNH2 related long QT syndrome

Journal of arrhythmia, 2020-02, Vol.36 (1), p.193-196

2020

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A genetic and developmental biological approach for a family with complex congenital heart diseases-evidence of digenic inheritance

Frontiers in cardiovascular medicine, 2023-04, Vol.10, p.1135141-1135141

2023

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A Novel SCN5A Mutation Found in a Familial Case of Long QT Syndrome Complicated by Severe Left Ventricular Dysfunction

Canadian journal of cardiology, 2017-04, Vol.33 (4), p.554.e5-554.e7

2017

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Poor outcomes in carriers of the RNF213 variant (p.Arg4810Lys) with pulmonary arterial hypertension

The Journal of heart and lung transplantation, 2020-02, Vol.39 (2), p.103-112

2020

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Sex-Dependent Phenotypic Variability of an SCN5A Mutation: Brugada Syndrome and Sick Sinus Syndrome

Journal of the American Heart Association, 2018-09, Vol.7 (18), p.e009387-e009387

2018

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Update of the genotype and phenotype of KMT2D and KDM6A by genetic screening of 100 patients with clinically suspected Kabuki syndrome

American journal of medical genetics. Part A, 2020-10, Vol.182 (10), p.2333-2344

2020

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Fra‐1/AP‐1 Impairs Inflammatory Responses and Chondrogenesis in Fracture Healing

Journal of bone and mineral research, 2009-12, Vol.24 (12), p.2056-2065

2009

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TET2 Variants in Japanese Patients With Pulmonary Arterial Hypertension

CJC open (Online), 2022-04, Vol.4 (4), p.416-419

2022

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Development of monomorphic ventricular tachycardia in a patient with fever‐induced Brugada syndrome

Journal of arrhythmia, 2018-08, Vol.34 (4), p.465-468

2018

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An RyR2 Mutation found in a family with a Short-coupled Variant of Torsade de Pointes

International journal of cardiology, 2017-01, Vol.227, p.367-369

2017

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Caffeine Intoxication in Pregnancy: Report of a case

Emphysematous cystitis successfully treated with hyperbaric oxygen therapy: case report

Successful Cardiac, Lung, and Kidney Transplantation from a Methanol-poisoned Donor

Successfully treated case of severe hypothermia secondary to myxedema coma

Epileptic Seizure from Ginkgo Nut Intoxication in an Adult

Extracorporeal cardiopulmonary resuscitation in out-of-hospital cardiac arrest patients by cannulating the right internal jugular vein for outflow

Caffeine Intoxication in Pregnancy; a case Report

Ictal Cardiorespiratory Arrest Associated with Status Epilepticus in Panayiotopoulos Syndrome

Blended phenotype of AP4E1 deficiency and Angelman syndrome caused by paternal isodisomy of chromosome 15

Omega-3 fatty acid epoxides produced by PAF-AH2 in mast cells regulate pulmonary vascular remodeling

Extracorporeal cardiopulmonary resuscitation in adult patients with out-of-hospital cardiac arrest: a retrospective large cohort multicenter study in Japan

Peripheral pulmonary stenosis with Noonan syndrome treated by balloon pulmonary angioplasty

TNFRSF13B c.226G>A (p.Gly76Ser) as a Novel Causative Mutation for Pulmonary Arterial Hypertension

Bulk and surface uniformity of magnetic and electronic structures in epitaxial W / Mn 3 Sn / MgO films revealed by fluorescence- and electron-yield x-ray magnetic circular dichroism

Mexiletine shortens the QT interval in a pedigree of KCNH2 related long QT syndrome

A genetic and developmental biological approach for a family with complex congenital heart diseases-evidence of digenic inheritance

Mutations in B3GALT6, which Encodes a Glycosaminoglycan Linker Region Enzyme, Cause a Spectrum of Skeletal and Connective Tissue Disorders

A Novel SCN5A Mutation Found in a Familial Case of Long QT Syndrome Complicated by Severe Left Ventricular Dysfunction

Poor outcomes in carriers of the RNF213 variant (p.Arg4810Lys) with pulmonary arterial hypertension

Sex-Dependent Phenotypic Variability of an SCN5A Mutation: Brugada Syndrome and Sick Sinus Syndrome

Update of the genotype and phenotype of KMT2D and KDM6A by genetic screening of 100 patients with clinically suspected Kabuki syndrome

Fra‐1/AP‐1 Impairs Inflammatory Responses and Chondrogenesis in Fracture Healing

TET2 Variants in Japanese Patients With Pulmonary Arterial Hypertension

Development of monomorphic ventricular tachycardia in a patient with fever‐induced Brugada syndrome

An RyR2 Mutation found in a family with a Short-coupled Variant of Torsade de Pointes

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