Kentaro Sawano - Publications

Early Pubertal Progression and Increased 11-Oxygenated Androgens in a Girl with Wiedemann-Steiner Syndrome and a KMT2A Variant: A Case Report.

Journal: Molecular syndromology

Published: January 29, 2026

Utility of the FT3-to-FT4 ratio as a screening marker for pediatric Graves' disease.

Journal: Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology

Published: February 14, 2025

De novo retrotransposon insertion into the FGFR1 gene in a boy with congenital hypogonadotropic hypogonadism: a case report.

Journal: Frontiers in endocrinology

Published: January 23, 2025

Atypical case of neonatal-onset Gaucher disease type 3b: A case report.

Journal: Molecular genetics and metabolism reports

Published: December 23, 2024

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

Journal: Children (Basel, Switzerland)

Published: August 24, 2024

Robust growth hormone responses to GH-releasing peptide 2 in adolescents.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: March 08, 2024

Hypocarnitinemia in twins after maternal pivalate-conjugated antibiotic therapy.

Journal: Pediatrics international : official journal of the Japan Pediatric Society

Published: October 09, 2023

A Study of Maternal Patients Diagnosed with Inborn Errors of Metabolism Due to Positive Newborn Mass Screening in Their Newborns.

Journal: Children (Basel, Switzerland)

Published: June 26, 2023

Klinefelter syndrome with penoscrotal transposition and diphallia: A case study.

Journal: Congenital anomalies

Published: December 30, 2022

Asymmetrical Graves' disease in children: potential usefulness of potassium iodide monotherapy.

Journal: BMJ case reports

Published: April 23, 2022

Infantile-Onset Isolated Neurohypophyseal Langerhans Cell Histiocytosis with Central Diabetes Insipidus: A Case Report.

Journal: Children (Basel, Switzerland)

Published: April 14, 2022

Expanding the phenotypic spectrum of ARCN1-related syndrome.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: December 10, 2021