Enteroendocrine Connections in Congenital Isolated GH Deficiency Due to a GHRH Receptor Gene Mutation

Autor: Cindi G. Marinho, Viviane C. Campos, Enaldo Vieira de Melo, Flávia Oliveira Costa, Manuel H. Aguiar-Oliveira, Djane A. Oliveira, Meirielly L.A. Barbosa, Mônica Cristina Nogueira, Margaret de Castro, Manuela A. Melo, Ívina E. S. Rocha, Ana Carolina Bueno, Nayra P. Damascena, Ângela C.G.B. Leal, Roberto Salvatori, Jinssica S.S. Dos Santos, Carla R. P. Oliveira, Elenilde G. Santos, Cynthia S Barros-Oliveira, Alécia A Oliveira-Santos, Paula F.C. Santos

Publikováno v: Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP

CONTEXT GH and IGF-1 are crucial for attainment of normal body size and regulation of food intake, nutrient storage, and insulin sensitivity. Enteroendocrine connections exist between the GH-IGF-1 axis and insulin, ghrelin, and glucagon-like peptide

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b811d2fdd5b40fcf552afc49f7bc533
https://pubmed.ncbi.nlm.nih.gov/30860584