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A Case of Aseptic Meningitis Without Skin Rash Caused by Oka Varicella Vaccine

The Pediatric infectious disease journal, 2022-01, Vol.41 (1), p.78-79

2022

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The iodide transporter Slc26a7 impacts thyroid function more strongly than Slc26a4 in mice

Scientific reports, 2022-07, Vol.12 (1), p.11259-11259, Article 11259

2022

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An infant with a heterozygous variant of ABCG5 presented with hypercholesterolemia only during breastfeeding

Clinical Pediatric Endocrinology, 2023, pp.2022-0075

2023

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Congenital goitrous hypothyroidism is caused by dysfunction of the iodide transporter SLC26A7

Communications biology, 2019-07, Vol.2 (1), p.270, Article 270

2019

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Regional Difference in Myelination in Monocarboxylate Transporter 8 Deficiency: Case Reports and Literature Review of Cases in Japan

Frontiers in neurology, 2021-07, Vol.12

2021

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Partial nephrogenic diabetes insipidus with a novel arginine vasopressin receptor 2 gene variant

Clinical Pediatric Endocrinology, 2022, Vol.31(1), pp.44-49

2022

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Molecular and clinical features of KATP‐channel neonatal diabetes mellitus in Japan

Pediatric diabetes, 2017-11, Vol.18 (7), p.532-539

2017

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Pregnancy outcome of Japanese patients with glucokinase–maturity‐onset diabetes of the young

Journal of diabetes investigation, 2019-11, Vol.10 (6), p.1586-1589

2019

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Questionnaire survey on severe hypoglycemia in pediatric patients with diabetes-English version

Diabetology international, 2024-08, Vol.15 (4), p.666-672

2024

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Incidence rate and characteristics of symptomatic vitamin D deficiency in children: a nationwide survey in Japan

Endocrine Journal, 2018, Vol.65(6), pp.593-599

2018

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Guidelines for Mass Screening of Congenital Hypothyroidism (2014 revision)

Clinical Pediatric Endocrinology, 2015, Vol.24(3), pp.107-133

2015

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Individual Clinically Diagnosed with CHARGE Syndrome but with a Mutation in KMT2D , a Gene Associated with Kabuki Syndrome: A Case Report

Frontiers in genetics, 2017-12, Vol.8, p.210-210

2017

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Guidelines for diagnosis and treatment of 21-hydroxylase deficiency (2014 revision)

Clinical Pediatric Endocrinology, 2015, Vol.24(3), pp.77-105

2015

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Endothelin receptor antagonist attenuates oxidative stress in a neonatal sepsis piglet model

Pediatric research, 2012-12, Vol.72 (6), p.600-605

2012

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Endothelin receptor antagonist attenuates inflammatory response and prolongs the survival time in a neonatal sepsis model

Intensive care medicine, 2010-12, Vol.36 (12), p.2132-2139

2010

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Clinical and genetic investigation of 136 Japanese patients with congenital hypothyroidism

Journal of Pediatric Endocrinology and Metabolism, 2020-05, Vol.33 (6), p.691-701

2020

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Japanese siblings with cartilage‐hair hypoplasia exhibiting different severity

Pediatrics international, 2023-01, Vol.65 (1), p.e15557-n/a

2023

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Edaravone, a Hydroxyl Radical Scavenger, Ameliorates the Severity of Pulmonary Hypertension in a Porcine Model of Neonatal Sepsis

The Tohoku Journal of Experimental Medicine, 2011, Vol.223(4), pp.235-241

2011

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Usefulness of insulin detemir in Japanese children with type 1 diabetes

Pediatrics international, 2012-12, Vol.54 (6), p.773-779

2012

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Clinical significance of heterozygous carriers associated with compensated hypothyroidism in R450H, a common inactivating mutation of the thyrotropin receptor gene in Japanese

Endocrine, 2006-12, Vol.30 (3), p.383-388

2006

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Possible Relationship between Elevated Plasma ACTH and Tall Stature in Familial Glucocorticoid Deficiency

The Tohoku Journal of Experimental Medicine, 2005, Vol.205(2), pp.123-131

2005

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Guidelines for Mass Screening of Congenital Hypothyroidism (2014 revision)

Clinical Pediatric Endocrinology, 2015-07, Vol.24 (3), p.107-133

2015

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Genotype–Phenotype Correlations in 30 Japanese Patients With Congenital Hypothyroidism Attributable to TG Defects

The journal of clinical endocrinology and metabolism, 2024-08, Vol.109 (9), p.2358-2365

2024

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Severity of Virilization of External Genitalia in Japanese Patients with Salt-wasting 21-hydroxylase Deficiency

The Tohoku Journal of Experimental Medicine, 2008, Vol.215(4), pp.341-348

2008

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An infant with a heterozygous variant of ABCG5 presented with hypercholesterolemia only during breastfeeding

Clinical Pediatric Endocrinology, 2023-04, Vol.32 (2), p.114-118

2023

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A Case of Aseptic Meningitis Without Skin Rash Caused by Oka Varicella Vaccine

The iodide transporter Slc26a7 impacts thyroid function more strongly than Slc26a4 in mice

An infant with a heterozygous variant of ABCG5 presented with hypercholesterolemia only during breastfeeding

Congenital goitrous hypothyroidism is caused by dysfunction of the iodide transporter SLC26A7

Regional Difference in Myelination in Monocarboxylate Transporter 8 Deficiency: Case Reports and Literature Review of Cases in Japan

Partial nephrogenic diabetes insipidus with a novel arginine vasopressin receptor 2 gene variant

Molecular and clinical features of KATP‐channel neonatal diabetes mellitus in Japan

Pregnancy outcome of Japanese patients with glucokinase–maturity‐onset diabetes of the young

Questionnaire survey on severe hypoglycemia in pediatric patients with diabetes-English version

Incidence rate and characteristics of symptomatic vitamin D deficiency in children: a nationwide survey in Japan

Guidelines for Mass Screening of Congenital Hypothyroidism (2014 revision)

Individual Clinically Diagnosed with CHARGE Syndrome but with a Mutation in KMT2D , a Gene Associated with Kabuki Syndrome: A Case Report

Guidelines for diagnosis and treatment of 21-hydroxylase deficiency (2014 revision)

Endothelin receptor antagonist attenuates oxidative stress in a neonatal sepsis piglet model

Endothelin receptor antagonist attenuates inflammatory response and prolongs the survival time in a neonatal sepsis model

Clinical and genetic investigation of 136 Japanese patients with congenital hypothyroidism

Japanese siblings with cartilage‐hair hypoplasia exhibiting different severity

Edaravone, a Hydroxyl Radical Scavenger, Ameliorates the Severity of Pulmonary Hypertension in a Porcine Model of Neonatal Sepsis

Usefulness of insulin detemir in Japanese children with type 1 diabetes

Clinical significance of heterozygous carriers associated with compensated hypothyroidism in R450H, a common inactivating mutation of the thyrotropin receptor gene in Japanese

Possible Relationship between Elevated Plasma ACTH and Tall Stature in Familial Glucocorticoid Deficiency

Guidelines for Mass Screening of Congenital Hypothyroidism (2014 revision)

Genotype–Phenotype Correlations in 30 Japanese Patients With Congenital Hypothyroidism Attributable to TG Defects

Severity of Virilization of External Genitalia in Japanese Patients with Salt-wasting 21-hydroxylase Deficiency

An infant with a heterozygous variant of ABCG5 presented with hypercholesterolemia only during breastfeeding

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