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Last Updated: 10/31/2025
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Found 140 publications
A case of Rabson-Mendenhall syndrome treated with empagliflozin combined with metformin
Journal: Zhonghua er ke za zhi = Chinese journal of pediatrics
Published: September 17, 2025
Genealogical Rabson-Mendenhall syndrome caused by INSR Gene Mutation.
Journal: American journal of physiology. Endocrinology and metabolism
Published: June 11, 2025
Rabson-Mendenhall Syndrome Nearly Misdiagnosed as Type 1 Diabetes Mellitus: A Case Report.
Journal: Cureus
Published: March 25, 2025
Donohue syndrome with a homozygous INSR exon 14 deletion: a case report.
Journal: Oxford medical case reports
Published: March 17, 2025
Case Report: The long-term effects of the empagliflozin therapy on glycemia and renal function in a patient with Rabson-Mendenhall syndrome caused by two heterozygous variants in INSR gene.
Journal: Frontiers in endocrinology
Published: January 13, 2025
Rabson-Mendenhall syndrome presented as severe acanthosis nigricans in an infant harboring novel mutations in the INSR gene: a case report.
Journal: Frontiers in pediatrics
Published: October 15, 2024
Congenital hyperinsulinism in the Ukraine: a 10-year national study.
Journal: Frontiers in endocrinology
Published: September 17, 2024
Editorial: Personalized therapies for monogenic diabetes.
Journal: Frontiers in genetics
Published: September 14, 2024
Insulin resistant diabetes mellitus in a girl with mild Rabson-Mendenhall syndrome: efficacy of sodium glucose co-transporter 2 inhibitor.
Journal: Diabetology international
Published: June 05, 2024
Rabson-Mendenhall Syndrome: Analysis of the Clinical Characteristics and Gene Mutations in 42 Patients.
Journal: Journal of the Endocrine Society
Published: December 15, 2023
A Novel Mutation in the INSR Gene Causes Severe Insulin Resistance and Rabson-Mendenhall Syndrome in a Paraguayan Patient.
Journal: International journal of molecular sciences
Published: November 07, 2023
Last Updated: 10/31/2025