GLP-1 Receptor Agonist Treatment in Morbid Obesity and Type 2 Diabetes Due to Pathogenic Homozygous Melanocortin-4 Receptor Mutation: A Case Report-Reference-Cited by-同舟云学术

GLP-1 Receptor Agonist Treatment in Morbid Obesity and Type 2 Diabetes Due to Pathogenic Homozygous Melanocortin-4 Receptor Mutation: A Case Report

Published:2020-04 Issue:1 Volume:1 Page:100006
ISSN:2666-3791
Container-title:Cell Reports Medicine
language:en
Short-container-title:Cell Reports Medicine

Author:

Iepsen Eva W.,Have Christian T.,Veedfald Simon^ORCID,Madsbad Sten^ORCID,Holst Jens J.,Grarup Niels^ORCID,Pedersen Oluf,Brandslund Ivan^ORCID,Holm Jens-Christian,Hansen Torben,Torekov Signe S.^ORCID

Funder

The Danish Diabetes Academy

Novo Nordisk Foundation

The Lundbeck Foundation

Augustinus Foundation

Region Zealand Health Scientific Research Foundation

Aase and Ejnar Danielsens Foundation

Michaelsen Foundation

Tripartite Immunometabolism Consortium

Publisher

Elsevier BV

Subject

General Biochemistry, Genetics and Molecular Biology

Reference26 articles.

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2. Dominant and recessive inheritance of morbid obesity associated with melanocortin 4 receptor deficiency;Farooqi;J. Clin. Invest.,2000

3. Melanocortin 4 receptor mutations in obese Czech children: studies of prevalence, phenotype development, weight reduction response, and functional analysis;Hainerová;J. Clin. Endocrinol. Metab.,2007

4. Prevalence of mutations and functional analyses of melanocortin 4 receptor variants identified among 750 men with juvenile-onset obesity;Larsen;J. Clin. Endocrinol. Metab.,2005

5. Patients with Obesity Caused by Melanocortin-4 Receptor Mutations Can Be Treated with a Glucagon-like Peptide-1 Receptor Agonist;Iepsen;Cell Metab.,2018

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