Keiko Aso - Publications

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

Longitudinal clinical course in patients with 5α-reductase type 2 deficiency treated with testosterone and dihydrotestosterone during infancy and puberty.

Journal: Endocrine journal

Published: October 10, 2022

Congenital hypogonadotropic hypogonadism complicated by neuroblastoma.

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

Published: November 29, 2021

ACTH-cortisol dissociation in patients with Kawasaki disease: a retrospective study.

Journal: Endocrine journal

Published: February 04, 2021

Predictive effect of antithyroid antibody for relapse of Graves' disease.

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

Published: January 12, 2021

Genome analyses and androgen quantification for an infant with 5α-reductase type 2 deficiency.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: November 26, 2020

Prednisolone therapy in prolonged cerebral edema due to diabetic ketoacidosis.

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

Published: November 15, 2018

Effect of treatment with epoprostenol and endothelin receptor antagonists on the development of thyrotoxicosis in patients with pulmonary arterial hypertension.

Journal: Endocrine journal

Published: September 12, 2017

Rapid diagnosis of prosthetic valve endocarditis from Janeway lesions in a transcatheter aortic valve implantation patient.

Journal: Journal of cardiology cases

Published: July 01, 2015

Thyroid Dysfunction in Neonates Born to Mothers Who Have Undergone Hysterosalpingography Involving an Oil-Soluble Iodinated Contrast Medium.

Journal: Hormone research in paediatrics

Published: May 12, 2015

Hypothyroidism caused by the combination of two heterozygous mutations: one in the TSH receptor gene the other in the DUOX2 gene.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: February 13, 2014

A 3-year-old girl with Graves' disease with hypoglycemia following transient adrenal hyporesponsiveness.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: February 08, 2012