Mayumi Enya
Gifu-shi, 5011194, Japan
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 13 publications
First Japanese Family With PDX1-MODY (MODY4): A Novel PDX1 Frameshift Mutation, Clinical Characteristics, and Implications.
Journal: Journal of the Endocrine Society
Published: August 18, 2021
Diagnosis and treatment of primary central nervous system lymphoma with the primary lesion in the hypothalamus: a case report.
Journal: BMC endocrine disorders
Published: July 11, 2020
L-Arginine prevents cereblon-mediated ubiquitination of glucokinase and stimulates glucose-6-phosphate production in pancreatic β-cells.
Journal: Communications biology
Published: March 11, 2020
Clinical manifestations of a sporadic maturity-onset diabetes of the young (MODY) 5 with a whole deletion of HNF1B based on 17q12 microdeletion.
Journal: Endocrine journal
Published: August 09, 2019
Periodontal Disease May be Associated With the Occurrence of Diabetic Retinopathy: A Subgroup Analysis of The Survey of the Diabetes Coordination Notebook in Gifu.
Journal: Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association
Published: April 12, 2019
Genetic Dissection and Clinical Features of MODY6 (NEUROD1-MODY).
Journal: Current diabetes reports
Published: February 23, 2019
Evaluation of the Diabetes Regional Coordination Path using the Diabetes Coordination Notebook in community-based diabetes care.
Journal: Diabetology international
Published: July 10, 2018
No novel, high penetrant gene might remain to be found in Japanese patients with unknown MODY.
Journal: Journal of human genetics
Published: February 02, 2018
Effectiveness of Sodium-Glucose Cotransporter-2 Inhibitor as an Add-on Drug to GLP-1 Receptor Agonists for Glycemic Control of a Patient with Prader-Willi Syndrome: A Case Report.
Journal: Diabetes therapy : research, treatment and education of diabetes and related disorders
Published: December 05, 2017
A first case of adrenomyeloneuropathy with mutation Y174S of the adrenoleukodystrophy gene.
Journal: Neuro endocrinology letters
Published: January 30, 2017
NEUROD1-deficient diabetes (MODY6): Identification of the first cases in Japanese and the clinical features.
Journal: Pediatric diabetes
Published: January 04, 2017
Association of genetic variants of the incretin-related genes with quantitative traits and occurrence of type 2 diabetes in Japanese.
Journal: Molecular genetics and metabolism reports
Published: June 13, 2014
Last Updated: 09/26/2026