Contribution of Clinical Evaluation in estimation of pre-test probability in the diagnosis of cushing syndrome under a Bayesian perspective (2011)
- Authors:
- USP affiliated authors: CASTRO, MARGARET DE - FMRP ; MOREIRA, AYRTON CUSTODIO - FMRP ; MARTINEZ, EDSON ZANGIACOMI - FMRP
- Unidade: FMRP
- Assunto: ENDOCRINOLOGIA
- Language: Inglês
- Imprenta:
- Publisher place: Chevy Chase
- Date published: 2011
- Source:
- Título do periódico: Endocrine Reviews
- ISSN: 0163-769X
- Volume/Número/Paginação/Ano: v. 32, suppl. 3, res. P1-633, 2011
- Conference titles: International Pituitary Congress
-
ABNT
CIPOLI, Daniel; MARTINEZ, Edson Zangiacomi; CASTRO, Margaret de; MOREIRA, Ayrton Custódio. Contribution of Clinical Evaluation in estimation of pre-test probability in the diagnosis of cushing syndrome under a Bayesian perspective. Endocrine Reviews[S.l: s.n.], 2011. -
APA
Cipoli, D., Martinez, E. Z., Castro, M. de, & Moreira, A. C. (2011). Contribution of Clinical Evaluation in estimation of pre-test probability in the diagnosis of cushing syndrome under a Bayesian perspective. Endocrine Reviews. Chevy Chase. -
NLM
Cipoli D, Martinez EZ, Castro M de, Moreira AC. Contribution of Clinical Evaluation in estimation of pre-test probability in the diagnosis of cushing syndrome under a Bayesian perspective. Endocrine Reviews. 2011 ; 32 -
Vancouver
Cipoli D, Martinez EZ, Castro M de, Moreira AC. Contribution of Clinical Evaluation in estimation of pre-test probability in the diagnosis of cushing syndrome under a Bayesian perspective. Endocrine Reviews. 2011 ; 32 - Late-night salivary cortisol has a better performance than urinary free cortisol in the diagnosis of Cushing's syndrome
- Clinical judgment to estimate pretest probability in the diagnosis of Cushing's syndrome under a Bayesian perspective
- Ontogeny of the synchronisation between adrenal clock genes, adrenal steroidogenesis-related genes and the circadian rhythm of the HPA axis in rats
- Peripheral clock system circadian imbalance in Cushing's disease
- Efetio fundador da mutação Q356X no gene CYP11B1 em pacientes com deficiência da '11beta'- hidroxilase
- O gene homeobox Hexx1 nos defeitos da linha média cerebral (DLMC)
- Diagnóstico laboratorial da Síndorme de Cushing
- Concentrações séricas de GH, IGF-I e IGFBP-3 na acromegalia tratada com octreotida sc e LAR
- Neoplasia endócrina múltipla tipo 2A (NEM 2A): estudo molecular e bioquímico
- Late night salivary cortisol (LNSF) versus 24-H urinary free cortisol (UFC) in the diagnosis of cushing's syndrome (CS): a concomitant samples collection study during three consecutive days
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