Mechanisms in endocrinology: a sense of time of the glucocorticoid circadian clock: from the ontogeny to the diagnosis of Cushing’s syndrome (2018)
- Authors:
- USP affiliated authors: MOREIRA, AYRTON CUSTODIO - FMRP ; ANTONINI, SONIR ROBERTO RAUBER - FMRP ; CASTRO, MARGARET DE - FMRP
- Unidade: FMRP
- DOI: 10.1530/eje-18-0102
- Subjects: HORMÔNIOS GLICOCORTICOIDES; SISTEMA HIPOTÁLAMO-HIPOFISÁRIO; RITMO CIRCADIANO
- Agências de fomento:
- Language: Inglês
- Imprenta:
- Source:
- Título: European Journal of Endocrinology
- ISSN: 0804-4643
- Volume/Número/Paginação/Ano: v. 179, n. 1, p. R1-R18, 2018
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
MOREIRA, Ayrton Custódio e ANTONINI, Sonir Roberto Rauber e CASTRO, Margaret de. Mechanisms in endocrinology: a sense of time of the glucocorticoid circadian clock: from the ontogeny to the diagnosis of Cushing’s syndrome. European Journal of Endocrinology, v. 179, n. 1, p. R1-R18, 2018Tradução . . Disponível em: https://doi.org/10.1530/eje-18-0102. Acesso em: 23 maio 2025. -
APA
Moreira, A. C., Antonini, S. R. R., & Castro, M. de. (2018). Mechanisms in endocrinology: a sense of time of the glucocorticoid circadian clock: from the ontogeny to the diagnosis of Cushing’s syndrome. European Journal of Endocrinology, 179( 1), R1-R18. doi:10.1530/eje-18-0102 -
NLM
Moreira AC, Antonini SRR, Castro M de. Mechanisms in endocrinology: a sense of time of the glucocorticoid circadian clock: from the ontogeny to the diagnosis of Cushing’s syndrome [Internet]. European Journal of Endocrinology. 2018 ; 179( 1): R1-R18.[citado 2025 maio 23 ] Available from: https://doi.org/10.1530/eje-18-0102 -
Vancouver
Moreira AC, Antonini SRR, Castro M de. Mechanisms in endocrinology: a sense of time of the glucocorticoid circadian clock: from the ontogeny to the diagnosis of Cushing’s syndrome [Internet]. European Journal of Endocrinology. 2018 ; 179( 1): R1-R18.[citado 2025 maio 23 ] Available from: https://doi.org/10.1530/eje-18-0102 - Time course of central precocious puberty development caused by an MKRN3 gene mutation: a prismatic care
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Informações sobre o DOI: 10.1530/eje-18-0102 (Fonte: oaDOI API)
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