Katsuyuki Matsui
Otsu, 5202192, Japan
Last Updated: 09/26/2026
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Found 13 publications
Risks of using standard reference ranges for carbohydrate and lipid metabolism in low-carbohydrate diets: insights from ketogenic diet therapy in children with refractory epilepsy.
Journal: Diabetology international
Published: December 24, 2025
Clinical practice guidelines for the management of differences of sex development in Japan.
Journal: Endocrine journal
Published: December 03, 2025
Clinical practice guidelines for the management of differences of sex development in Japan.
Journal: Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology
Published: August 13, 2025
Questionnaire survey on severe hypoglycemia in pediatric patients with diabetes-English version.
Journal: Diabetology international
Published: June 05, 2024
Use of a long-term continuous glucose monitor for predicting sulfonylurea dose in patients with neonatal diabetes mellitus: a case series.
Journal: Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology
Published: October 05, 2023
Ketogenic diet for refractory epilepsy with MEHMO syndrome: Caution for acute necrotizing pancreatitis.
Journal: Brain & development
Published: September 28, 2020
Pregnancy outcome of Japanese patients with glucokinase-maturity-onset diabetes of the young.
Journal: Journal of diabetes investigation
Published: December 04, 2018
Genotype of UGT1A1 and phenotype correlation between Crigler-Najjar syndrome type II and Gilbert syndrome.
Journal: Journal of gastroenterology and hepatology
Published: February 10, 2015
Increased expression of GAP43 in interneurons in a rat model of experimental polymicrogyria.
Journal: Journal of child neurology
Published: May 05, 2014
Bilirubin uridine diphosphate-glucuronosyltransferase variation is a genetic basis of breast milk jaundice.
Journal: The Journal of pediatrics
Published: October 10, 2013
A novel large deletion (exons 12, 13) and a missense mutation (p.G46R) in the PAH in a Japanese patient with phenylketonuria.
Journal: World journal of pediatrics : WJP
Published: March 29, 2013
Last Updated: 09/26/2026