| Combined pituitary hormone deficiency caused by PROP1 mutations: update 20 years post-discovery FA Correa, M Nakaguma, JLO Madeira, MY Nishi, MG Abrão, AAL Jorge, ... Archives of Endocrinology and Metabolism 63, 167-174, 2019 | 31 | 2019 |
| Molecular analysis of brazilian patients with combined pituitary hormone deficiency and orthotopic posterior pituitary lobe reveals eight different PROP1 alterations … JLO Madeira, MY Nishi, M Nakaguma, AF Benedetti, IP Biscotto, ... Clinical endocrinology 87 (6), 725-732, 2017 | 16 | 2017 |
| A severe phenotype of Kennedy disease associated with a very large CAG repeat expansion. JLO Madeira, ABC Souza, FS Cunha, RL Batista, NL Gomes, ... Muscle & nerve 57 (1), E95-E97, 2017 | 13 | 2017 |
| A homozygous point mutation in the GH1 promoter (c.-223C>T) leads to reduced GH1 expression in siblings with isolated GH deficiency (IGHD) JLO Madeira, AAL Jorge, RM Martin, LR Montenegro, MM Franca, ... European journal of endocrinology 175 (2), K7-K15, 2016 | 12 | 2016 |
| Homeostasis in networks with multiple input nodes and robustness in bacterial chemotaxis JLO Madeira, F Antoneli Journal of Nonlinear Science 32 (3), 37, 2022 | 7 | 2022 |
| Homeostasis in networks with multiple inputs JL de Oliveira Madeira, F Antoneli Journal of Mathematical Biology 89 (2), 17, 2024 | 1 | 2024 |
| Homozygous CDH2 variant may be associated with hypopituitarism without neurological disorders NGBP Ferreira, JLO Madeira, P Gergics, R Kertsz, JM Marques, ... Endocrine Connections 12 (8), 2023 | 1 | 2023 |
| Análise de um radioimunoensaio iodado para determinação de 11-deoxicortisol JLO Madeira, LZ Bussmann, HP Lima-Valassi, BB Mendonça Arquivos Brasileiros de Endocrinologia & Metabologia 58 (3), 232-236, 2014 | 1 | 2014 |
| Analysis of an iodide radioimmunoassay for 11-deoxicortisol measurement JLO Madeira, LZ Bussmann, HP Lima-Valassi, BB Mendonça Arquivos Brasileiros de Endocrinologia e Metabologia, 2014 | 1 | 2014 |
| Extensive Molecular Diagnosis in a Large Cohort of Androgen Insensitivity Syndrome RL Batista, MY Nishi, ADS Rodrigues, NL Gomes, JA Faria, IJP Arnhold, ... 99th Annual Meeting of the Endocrine Society, 2017 | | 2017 |
| Reversible Pituitary Function after Linear Growth in Patients with Congenital Hypopituitarism IP Biscotto, JLO Madeira, F Correa, AP Otto, EF Costalonga, MM Franca, ... 99th Annual Meeting of the Endocrine Society, 2017 | | 2017 |
| PARTIAL RECOVERY OF PITUITARY FUNCTION AFTER LINEAR GROWTH IN PATIENTS WITH CONGENITAL COMBINED PITUITARY HORMONE DEFICIENCY (CPHD) JLO Madeira, IP Biscotto, FA Correa, AP Otto, EF Costalonga, MM Franca, ... KARGER, 2017 | | 2017 |
| Molecular analysis of brazilian patients with combined pituitary hormone deficiency (CPHD) and orthotopic posterior pituitary lobe (OPP) reveals 8 different PROP1 alterations … JLO Madeira, AAL Jorge, BB Mendonça Hormone research in paediatrics 88, 43-44, 2017 | | 2017 |
| Aromatase excess syndrome (AES) in a 10-year old girl with gigantomastia JLO Madeira, CC Silva, AP Otto, EB Trarbach, MY Nishi, M Gianotti, ... Hormone Research in Paediatrics, 2017 | | 2017 |
| Hipopituitarismo em crianças e adultos LRS CARVALHO, CV CHANG, FA CORRêA, JLO MADEIRA, MF GUZZO, ... Endocrinologia: princípios e práticas [2ed.], 2017 | | 2017 |
| A Novel OTX2 Mutation, P. H230L, Causes Hypopituitarism with Incomplete Penetrance: Exome Sequencing to Identify Modifier Genes J Madeira, M Moreira, M Franca, A Otto, F Correa, I Arnhold, B Mendonca, ... Hormone Research in Paediatrics, 2015 | | 2015 |
| A Homozygous Point Mutation in the GH1 Promoter (-161T> C) Leads to Reduced GH Expression in Siblings with Isolated GH Deficiency (IGHD) L Carvalho, J Madeira, R Martin, L Montenegro, M Franca, E Costalonga, ... KARGER, 2015 | | 2015 |
| A Homozygous Point Mutation in the GH1 Promoter ([mdash] 161T [gt] C) Leads to Reduced GH Expression in Siblings with Isolated GH Deficiency J Madeira, R Martin, L Montenegro, M Franca, E Costalonga, F Correa, ... European Society for Paediatric Endocrinology, 2014 | | 2014 |
| Deficiências hipotálamo-hipofisárias múltiplas por mutações nos genes HESX1 e SOX3 LR Carvalho, M Moreira, JLO Madeira, BB MENDONçA, IJP Arnhold Investigação da baixa estatura: do fenótipo ao genótipo, 2012 | | 2012 |
| In vitro evaluation of an intraventricular axial flow pump for mechanical circulatory support LF KUBRUSLY, AF MARTINS, J MADEIRA, S Savytzky, D WOLLMAN, ... Brazilian Journal of Cardiovascular Surgery 15, 169-172, 2000 | | 2000 |
Berenice Bilharinho de MendonçaFaculdade de Medicina da Universidade de São PauloVerified email at usp.br
