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Portuguese version of the Literacy Independent Cognitive Assessment (LICA) instrument in the evaluation of individuals aged 50 years or older with Itabaianinha syndrome.
Santos LB, Kellner M, Lisboa W, Faro A, Oliveira CRP, Batista VO, Oliveira-Santos AA, de Brito ÍVA, Marinho CG, Campos VC, Villar-Gouy KR, Leal ÂC, Amorim RS, Melo EV, Santos EG, Salvatori R, Aguiar-Oliveira MH. Santos LB, et al. Among authors: marinho cg. Arch Endocrinol Metab. 2024 Aug 13;68:e230265. doi: 10.20945/2359-4292-2023-0265. eCollection 2024. Arch Endocrinol Metab. 2024. PMID: 39420931 Free PMC article.
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: marinho cg. 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: marinho cg. Endocrine. 2021 Jul;73(1):160-165. doi: 10.1007/s12020-021-02700-6. Epub 2021 Mar 26. Endocrine. 2021. PMID: 33770382
Quantitative measures of the vascular and neural components of the retina in adult individuals with congenital and untreated growth hormone deficiency.
Menezes NV, Barros-Oliveira CS, Salvatori R, Gois VC, Marinho CG, Oliveira CRP, Campos VC, Oliveira-Santos AA, Santos-Júnior HT, Santos EG, Melo EV, Faro ACN, Oliveira NV, Gumes-Felix HM, Melo GB, Aguiar-Oliveira MH. Menezes NV, et al. Among authors: marinho cg. Int J Retina Vitreous. 2022 Oct 1;8(1):72. doi: 10.1186/s40942-022-00408-x. Int J Retina Vitreous. 2022. PMID: 36183116 Free PMC article.
Sweat and vitamin D status in congenital, lifetime, untreated GH deficiency.
Barros-Oliveira CS, Salvatori R, Dos Santos JSS, Santos PFC, Oliveira-Santos AA, Marinho CG, Santos EG, Leal ÂCGB, Campos VC, Damascena NP, Oliveira CRP, Aguiar-Oliveira MH. Barros-Oliveira CS, et al. Among authors: marinho cg. Endocrine. 2019 Sep;65(3):710-713. doi: 10.1007/s12020-019-01998-7. Epub 2019 Jul 10. Endocrine. 2019. PMID: 31292841
Cerebral vasoreactivity, a surrogate marker of cerebrovascular disease, is not impaired in subjects with lifetime, untreated, congenital isolated GH deficiency.
Marinho CG, Melo HA, Salvatori R, Nunes MAP, Oliveira CRP, Campos VC, Barros-Oliveira CS, Oliveira-Santos AA, Menezes NV, Santos-Júnior HT, Santos EG, Melo MA, Oliveira JLM, Melo EV, Aguiar-Oliveira MH. Marinho CG, et al. Endocrine. 2020 Nov;70(2):388-395. doi: 10.1007/s12020-020-02415-0. Epub 2020 Jul 12. Endocrine. 2020. PMID: 32656695
Circulating microRNA profile in humans and mice with congenital GH deficiency.
Saccon TD, Schneider A, Marinho CG, Nunes ADC, Noureddine S, Dhahbi J, Nunez Lopez YO, LeMunyan G, Salvatori R, Oliveira CRP, Oliveira-Santos AA, Musi N, Bartke A, Aguiar-Oliveira MH, Masternak MM. Saccon TD, et al. Among authors: marinho cg. Aging Cell. 2021 Jul;20(7):e13420. doi: 10.1111/acel.13420. Epub 2021 Jun 12. Aging Cell. 2021. PMID: 34118183 Free PMC article.
15 results