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Enteroendocrine Connections in Congenital Isolated GH Deficiency Due to a GHRH Receptor Gene Mutation.
Oliveira-Santos AA, Salvatori R, Nogueira MC, Bueno AC, Barros-Oliveira CS, Leal ÂCGB, Marinho CG, Damascena NP, Oliveira DA, Melo MA, Oliveira CRP, da Costa FO, Dos Santos JSS, Santos PFC, Campos VC, Santos EG, Melo EV, Barbosa MLA, Rocha IES, de Castro M, Aguiar-Oliveira MH. Oliveira-Santos AA, et al. Among authors: bueno ac. J Clin Endocrinol Metab. 2019 Jul 1;104(7):2777-2784. doi: 10.1210/jc.2019-00094. J Clin Endocrinol Metab. 2019. PMID: 30860584
Reduced fibroblast growth factor 21 and β-Klotho secretion in untreated congenital isolated GH deficiency.
Oliveira-Santos AA, Salvatori R, Bueno AC, Nogueira MC, Campos VC, Melo MA, Oliveira CRP, Barros-Oliveira CS, Marinho CG, Damascena NP, Santos EG, Melo EV, de Paula FJA, de Castro M, Aguiar-Oliveira MH. Oliveira-Santos AA, et al. Among authors: bueno ac. Endocrine. 2021 Jul;73(1):160-165. doi: 10.1007/s12020-021-02700-6. Epub 2021 Mar 26. Endocrine. 2021. PMID: 33770382
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