Ryosei Iemura

Chiba, Japan

Last Updated: 09/26/2026

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Found 11 publications

Gonadotropin Suppression During Mini-Puberty as an Early Biomarker of Classic 21-Hydroxylase Deficiency.

Gonadotropin Suppression During Mini-Puberty as an Early Biomarker of Classic 21-Hydroxylase Deficiency.

Journal: Endocrinology, diabetes & metabolism
Published: June 27, 2026

Congenital adrenal hypoplasia with neurodevelopmental delay due to contiguous Xp21 deletion: a case series with review of literature.

Congenital adrenal hypoplasia with neurodevelopmental delay due to contiguous Xp21 deletion: a case series with review of literature.

Journal: Endocrine journal
Published: November 24, 2025

Severe hepatic steatosis contributes to liver dysfunction in non-obese patients with insulin-resistant diabetes mellitus after hematopoietic stem cell transplantation.

Severe hepatic steatosis contributes to liver dysfunction in non-obese patients with insulin-resistant diabetes mellitus after hematopoietic stem cell transplantation.

Journal: Pediatrics international : official journal of the Japan Pediatric Society
Published: December 17, 2024

Impact of the COVID-19 Pandemic on Epidemiological Trends in Pediatric Cervical Abscess-Forming Infections.

Impact of the COVID-19 Pandemic on Epidemiological Trends in Pediatric Cervical Abscess-Forming Infections.

Journal: Microorganisms
Published: December 05, 2024

Clinical features of neonatal Graves' disease revealed by twelve cases that require- antithyroid therapy.

Clinical features of neonatal Graves' disease revealed by twelve cases that require- antithyroid therapy.

Journal: Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology
Published: November 12, 2024

Classic 21-hydroxylase deficiency in opposite-sex twins.

Classic 21-hydroxylase deficiency in opposite-sex twins.

Journal: Pediatrics international : official journal of the Japan Pediatric Society
Published: August 14, 2024

Familial and early recurrent pheochromocytoma in a child with a novel in-frame duplication variant of VHL.

Familial and early recurrent pheochromocytoma in a child with a novel in-frame duplication variant of VHL.

Journal: Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology
Published: February 13, 2024

Clinical management of diazoxide-unresponsive congenital hyperinsulinism: A single-center experience.

Clinical management of diazoxide-unresponsive congenital hyperinsulinism: A single-center experience.

Journal: Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology
Published: January 09, 2024

Phenotypic Variation in 46,XX Disorders of Sex Development due to the Fourth Zinc Finger Domain Variant of WT1: A Familial Case Report.

Phenotypic Variation in 46,XX Disorders of Sex Development due to the Fourth Zinc Finger Domain Variant of WT1: A Familial Case Report.

Journal: Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation
Published: September 07, 2022

BMP2 is a potential causative gene for isolated dextrocardia situs solitus.

BMP2 is a potential causative gene for isolated dextrocardia situs solitus.

Journal: European journal of medical genetics
Published: July 20, 2022

Autonomously functioning thyroid nodule due to a somatic TSHR mutation.

Autonomously functioning thyroid nodule due to a somatic TSHR mutation.

Journal: Pediatrics international : official journal of the Japan Pediatric Society
Published: December 02, 2021
Showing 1-11 of 11

Last Updated: 09/26/2026