Open AccessMON-437 Enteroendocrine Connections in Congenital Isolated GH Deficiency Due to GHRH Receptor Gene Mutation
Author(s) -
Alécia A Oliveira-Santos,
Mônica Cristiogueira,
Margaret de Castro,
Roberto Salvatori,
Ana Carolina Arruda,
Cind G. Marinho,
Cynthia S Barros-Oliveira,
Ângela C O Leal,
Nicole Prata Damascena,
Djane A. Oliveira,
Manuela A. Melo,
Carla R. P. Oliveira,
F. Costa,
Jessica Ss dos Santos,
Paula F.C. Santos,
Viviane C. Campos,
Elenilde G. Santos,
Manuel H. AguiarOliveira
Publication year - 2019
Publication title -
journal of the endocrine society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.046
H-Index - 20
ISSN - 2472-1972
DOI - 10.1210/js.2019-mon-437
Subject(s) - endocrinology , medicine , ghrelin , ighd , insulin , enteroendocrine cell , incretin , biology , dyslipidemia , hormone , endocrine system , type 2 diabetes , growth hormone deficiency , diabetes mellitus , growth hormone