Validation of a radioimmunoassay for 11-deoxycortisol measurement for the diagnosis of hyperandrogenic disorders

• Grant number: 10/05188-0
• Support Opportunities: Scholarships in Brazil - Scientific Initiation
• Start date: June 01, 2010
• End date: May 31, 2013
• Field of knowledge: Health Sciences - Medicine - Medical Clinics
• Principal Investigator: Berenice Bilharinho de Mendonça
• Grantee: João Luiz de Oliveira Madeira
• Host Institution: Faculdade de Medicina (FM). Universidade de São Paulo (USP). São Paulo , SP, Brazil
• Associated research grant: 05/04726-0 - Molecular characterization of congenital endocrine diseases that affect growth and development, AP.TEM

Scientific publications

(References retrieved automatically from Web of Science and SciELO through information on FAPESP grants and their corresponding numbers as mentioned in the publications by the authors)

JOÃO LUIZ DE OLIVEIRA MADEIRA; LUCIANE ZGODA BUSSMANN; HELENA PANTELIOU LIMA-VALASSI; BERENICE BILHARINHO DE MENDONÇA. Análise de um radioimunoensaio iodado para determinação de 11-deoxicortisol. Arquivos Brasileiros de Endocrinologia e Metabologia, v. 58, n. 3, p. 232-236, 2014-04-00. (10/05188-0)

MADEIRA, JOAO L. O.; JORGE, ALEXANDER A. L.; MARTIN, REGINA M.; MONTENEGRO, LUCIANA R.; FRANCA, MARCELA M.; COSTALONGA, EVERLAYNY F.; CORREA, FERNANDA A.; OTTO, ALINE P.; ARNHOLD, IVO J. P.; FREITAS, HELAYNE S.; et al. A homozygous point mutation in the GH1 promoter (c.-223C > T) leads to reduced GH1 expression in siblings with isolated GH deficiency (IGHD). EUROPEAN JOURNAL OF ENDOCRINOLOGY, v. 175, n. 2, p. K7-K15, AUG 2016. (13/03236-5, 10/05188-0)