Nao Shibata - Publications

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

Journal: Molecular genetics and metabolism reports

Published: December 23, 2024

Cutoff value of serum 25-hydroxyvitamin D leading to vitamin D deficiency for children in Japan.

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

Published: September 30, 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

Clinical and molecular analyses of isolated central congenital hypothyroidism based on a survey conducted in Japan.

Journal: Endocrine journal

Published: March 10, 2024

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

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: March 08, 2024

Successful Multimodal Treatment of Intracranial Growing Teratoma Syndrome with Malignant Features.

Journal: Current oncology (Toronto, Ont.)

Published: February 16, 2024

Reliable detection of genetic alterations in cyst fluid DNA for the diagnosis of brain tumors.

Journal: Journal of neuro-oncology

Published: November 10, 2023

Incidence and Risk Factors for Adrenal Crisis in Pediatric-onset Adrenal Insufficiency: A Prospective Study.

Journal: The Journal of clinical endocrinology and metabolism

Published: August 03, 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

Peripheral precocious puberty in a girl with an intracranial hCG-producing tumor: case report and literature review.

Journal: Endocrine journal

Published: July 19, 2021

A Japanese family with a heterozygous novel mutation in the Indian hedgehog gene exhibiting a broad spectrum of clinical features and radiological findings.

Journal: Congenital anomalies

Published: April 30, 2021