Hiroko Yagi - Publications

Efficacy and Safety of Glecaprevir/Pibrentasvir in Children Aged 3-11 Years With Chronic Hepatitis C: A Real-World, Prospective, Multicenter Study in Japan.

Journal: Hepatology research : the official journal of the Japan Society of Hepatology

Published: June 12, 2025

Screening for imprinting disorders in 58 patients with clinically diagnosed idiopathic short stature.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: April 17, 2020

Relaxin-3 regulates corticotropin-releasing factor gene expression in cultured rat hypothalamic 4B cells.

Journal: Neuroscience letters

Published: September 24, 2018

A familial case of spondyloepiphyseal dysplasia tarda caused by a novel splice site mutation in TRAPPC2.

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

Published: February 20, 2018

Regulation of gonadotropins by urocortin 2 in gonadotropic tumor LβT2 cells.

Journal: Neuroscience letters

Published: July 14, 2017

Five cases of childhood-onset Graves' disease treated with either surgery or radio-iodine therapy.

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

Published: April 10, 2017

Gradually increasing ethinyl estradiol for Turner syndrome may produce good final height but not ideal BMD.

Journal: Endocrine journal

Published: December 06, 2016

A novel heterozygous intronic mutation in POU1F1 is associated with combined pituitary hormone deficiency.

Journal: Endocrine journal

Published: November 26, 2016

Syndromic disorder of sex development due to a novel hemizygous mutation in the carboxyl-terminal domain of ATRX.

Journal: Human genome variation

Published: November 16, 2016

A case of transient neonatal diabetes due to a novel mutation in ABCC8.

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

Published: August 02, 2016

Novel heterozygous mutation in the extracellular domain of FGFR1 associated with Hartsfield syndrome.

Journal: Human genome variation

Published: May 25, 2016

Early-onset urological disorders due to Wolfram syndrome: A case of neonatal onset.

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

Published: September 11, 2015