Open AccessMON-437 Enteroendocrine Connections in Congenital Isolated GH Deficiency Due to GHRH Receptor Gene Mutation
Author(s) -
Alécia A. OliveiraSantos,
Mônica Cristiogueira,
Margaret de Castro,
Roberto Salvatori,
Ana Carolina Arruda,
Cind G. Marinho,
Cynthia S. Barros-Oliveira,
Ângela C. Leal,
Nayra P. Damascena,
D A S Oliveira,
Manuela A. Melo,
Carla R. P. Oliveira,
Flávia Oliveira da 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
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