Rie Yamaguchi
Hamamatsu, Japan
Last Updated: 09/26/2026
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Found 10 publications
Familial campomelic dysplasia due to maternal germinal mosaicism.
Journal: Congenital anomalies
Published: November 13, 2017
Reciprocal Regulation of 11β-HSDs May Predict Steroid Sensitivity in Childhood Nephrotic Syndrome.
Journal: Pediatrics
Published: May 24, 2016
Combined steroidogenic characters of fetal adrenal and Leydig cells in childhood adrenocortical carcinoma.
Journal: The Journal of steroid biochemistry and molecular biology
Published: November 19, 2015
Impact of a novel homozygous mutation in nicotinamide nucleotide transhydrogenase on mitochondrial DNA integrity in a case of familial glucocorticoid deficiency.
Journal: BBA clinical
Published: August 27, 2015
Development of waist circumference percentiles for Japanese children and an examination of their screening utility for childhood metabolic syndrome: a population-based cross-sectional study.
Journal: BMC public health
Published: April 03, 2015
Urinary myo-inositol levels in Japanese schoolchildren with normal glucose tolerance.
Journal: Journal of pediatric endocrinology & metabolism : JPEM
Published: March 04, 2015
Japanese founder duplications/triplications involving BHLHA9 are associated with split-hand/foot malformation with or without long bone deficiency and Gollop-Wolfgang complex.
Journal: Orphanet journal of rare diseases
Published: April 15, 2014
Identification of AP2S1 mutation and effects of low calcium formula in an infant with hypercalcemia and hypercalciuria.
Journal: The Journal of clinical endocrinology and metabolism
Published: October 02, 2013
A novel homozygous mutation of the nicotinamide nucleotide transhydrogenase gene in a Japanese patient with familial glucocorticoid deficiency.
Journal: Endocrine journal
Published: March 12, 2013
The lipid fraction of human milk initiates adipocyte differentiation in 3T3-L1 cells.
Journal: Early human development
Published: February 05, 2013
Showing 1-10 of 10
Last Updated: 09/26/2026