Ichiro Miyata

Tokyo, 1058461, Japan

Last Updated: 09/26/2026

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Found 10 publications

Growth hormone resistance induced by amino acid deprivation in fao cells is independent of FGF21.

Growth hormone resistance induced by amino acid deprivation in fao cells is independent of FGF21.

Journal: Biochemical and biophysical research communications

Published: February 28, 2024

Essential Amino Acid Intake Is Required for Sustaining Serum Insulin-like Growth Factor-I Levels but Is Not Necessarily Needed for Body Growth.

Essential Amino Acid Intake Is Required for Sustaining Serum Insulin-like Growth Factor-I Levels but Is Not Necessarily Needed for Body Growth.

Journal: Cells

Published: March 25, 2022

Novel biallelic splice-site BBS1 variants in Bardet-Biedle syndrome: a case report of the first Japanese patient.

Novel biallelic splice-site BBS1 variants in Bardet-Biedle syndrome: a case report of the first Japanese patient.

Journal: Documenta ophthalmologica. Advances in ophthalmology

Published: December 24, 2019

Fetal Goitrous Hypothyroidism and Polyhydramnios in a Patient with Compound Heterozygous DUOXA2 Mutations.

Fetal Goitrous Hypothyroidism and Polyhydramnios in a Patient with Compound Heterozygous DUOXA2 Mutations.

Journal: Hormone research in paediatrics

Published: April 11, 2018

Discovery of GnIH and Its Role in Hypothyroidism-Induced Delayed Puberty.

Discovery of GnIH and Its Role in Hypothyroidism-Induced Delayed Puberty.

Journal: Endocrinology

Published: March 29, 2017

Structural Basis and Genotype-Phenotype Correlations of INSR Mutations Causing Severe Insulin Resistance.

Structural Basis and Genotype-Phenotype Correlations of INSR Mutations Causing Severe Insulin Resistance.

Journal: Diabetes

Published: March 09, 2017

A novel NR3C2 mutation in a Japanese patient with the renal form of pseudohypoaldosteronism type 1.

A novel NR3C2 mutation in a Japanese patient with the renal form of pseudohypoaldosteronism type 1.

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

Published: October 06, 2015

Three novel mutations of the MCT8 (SLC16A2) gene: individual and temporal variations of endocrinological and radiological features.

Three novel mutations of the MCT8 (SLC16A2) gene: individual and temporal variations of endocrinological and radiological features.

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

Published: October 05, 2015

Atypical clinical features of children with central nervous system tumor: Delayed diagnosis and switch in handedness.

Atypical clinical features of children with central nervous system tumor: Delayed diagnosis and switch in handedness.

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

Published: August 13, 2015

Treatment situation of male hypogonadotropic hypogonadism in pediatrics and proposal of testosterone and gonadotropins replacement therapy protocols.

Treatment situation of male hypogonadotropic hypogonadism in pediatrics and proposal of testosterone and gonadotropins replacement therapy protocols.

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

Published: May 28, 2014

Showing 1-10 of 10

Last Updated: 09/26/2026