Akihisa Nitta - Publications

Endocrine Characteristics of 246 Cases of Childhood-Onset Anorexia Nervosa in Japan: A Single-Center Experience.

Journal: Cureus

Published: August 24, 2025

A case of early diagnosis of congenital multisystem langerhans cell histiocytosis with thymic involvement triggered by newborn screening.

Journal: Immunological medicine

Published: June 13, 2025

A case report of odonto-hypophosphatasia with a novel variant in the ALPL gene.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: December 13, 2023

Discordant responses of bone formation and absorption markers in Japanese infants with vitamin D deficiency: a comprehensive matched case-control study.

Journal: JBMR plus

Published: September 13, 2023

Perinatal and neonatal characteristics of Prader-Willi syndrome in Japan.

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

Published: December 23, 2022

Primary hyperparathyroidism in a child with abdominal pain and hematuria.

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

Published: February 01, 2021

Successful treatment of Gaucher disease type 1 by enzyme replacement therapy over a 10-year duration in a Japanese pediatric patient: A case report.

Journal: Experimental and therapeutic medicine

Published: February 20, 2020

Fetal Bone Formation Is Decreased from Middle Pregnancy to Birth.

Journal: The Tohoku journal of experimental medicine

Published: June 07, 2016