| TAC3/TACR3 Mutations Reveal Preferential Activation of Gonadotropin-Releasing Hormone Release by Neurokinin B in Neonatal Life Followed by Reversal in … E Gianetti, C Tusset, SD Noel, MG Au, AA Dwyer, VA Hughes, AP Abreu, ... The Journal of Clinical Endocrinology & Metabolism 95 (6), 2857-2867, 2010 | 299 | 2010 |
| The importance of autosomal genes in Kallmann syndrome: genotype-phenotype correlations and neuroendocrine characteristics LMB Oliveira, SB Seminara, M Beranova, FJ Hayes, SB Valkenburgh, ... The Journal of Clinical Endocrinology & Metabolism 86 (4), 1532-1538, 2001 | 272 | 2001 |
| 46, XY disorders of sex development (DSD) BB Mendonca, S Domenice, IJP Arnhold, EMF Costa Clinical endocrinology 70 (2), 173-187, 2009 | 225 | 2009 |
| Clinical, hormonal, behavioral, and genetic characteristics of androgen insensitivity syndrome in a Brazilian cohort: five novel mutations in the androgen receptor gene KFS Melo, BB Mendonca, AEC Billerbeck, EMF Costa, M Inácio, ... The Journal of Clinical Endocrinology & Metabolism 88 (7), 3241-3250, 2003 | 209 | 2003 |
| Male pseudohermaphroditism due to steroid 5alpha-reductase 2 deficiency. Diagnosis, psychological evaluation, and management. BB Mendonca, M Inacio, EM Costa, IJ Arnhold, FA Silva, W Nicolau, ... Medicine 75 (2), 64-76, 1996 | 169 | 1996 |
| Spironolactone versus clonidine as a fourth-drug therapy for resistant hypertension: the ReHOT randomized study (Resistant Hypertension Optimal Treatment) EM Krieger, LF Drager, DMA Giorgi, AC Pereira, JAS Barreto-Filho, ... Hypertension 71 (4), 681-690, 2018 | 158 | 2018 |
| Effects of endocrine disruptors in the development of the female reproductive tract EMF Costa, PM Spritzer, A Hohl, TASS Bachega Arquivos Brasileiros de Endocrinologia & Metabologia 58, 153-161, 2014 | 147 | 2014 |
| Loss-of-function mutations in the genes encoding prokineticin-2 or prokineticin receptor-2 cause autosomal recessive Kallmann syndrome AP Abreu, EB Trarbach, M de Castro, EM Frade Costa, B Versiani, ... The Journal of Clinical Endocrinology & Metabolism 93 (10), 4113-4118, 2008 | 136 | 2008 |
| Androgen insensitivity syndrome: a review RL Batista, EMF Costa, AS Rodrigues, NL Gomes, JA Faria Jr, MY Nishi, ... Archives of endocrinology and metabolism 62, 227-235, 2018 | 135 | 2018 |
| Novel fibroblast growth factor receptor 1 mutations in patients with congenital hypogonadotropic hypogonadism with and without anosmia EB Trarbach, EMF Costa, B Versiani, M de Castro, MTM Baptista, ... The Journal of Clinical Endocrinology & Metabolism 91 (10), 4006-4012, 2006 | 130 | 2006 |
| The effects on Trypanosoma cruzi of novel synthetic naphthoquinones are mediated by mitochondrial dysfunction RFS Menna-Barreto, RLS Goncalves, EM Costa, RSF Silva, AV Pinto, ... Free Radical Biology and Medicine 47 (5), 644-653, 2009 | 124 | 2009 |
| Two novel mutations in the gonadotropin-releasing hormone receptor gene in Brazilian patients with hypogonadotropic hypogonadism and normal olfaction EMF Costa, GY Bedecarrats, BB Mendonca, IJP Arnhold, UB Kaiser, ... The Journal of Clinical Endocrinology & Metabolism 86 (6), 2680-2686, 2001 | 122 | 2001 |
| Male Pseudohermaphroditism due to 17 [beta]-Hydroxysteroid Dehydrogenase 3 Deficiency: Diagnosis, Psychological Evaluation, and Management. BB Mendonca, M Inacio, IJP Arnhold, EMF Costa, W Bloise, RM Martin, ... Medicine 79 (5), 299-309, 2000 | 119 | 2000 |
| P450c17 Deficiency in Brazilian Patients: Biochemical Diagnosis through Progesterone Levels Confirmed by CYP17 Genotyping RM Martin, CJ Lin, EMF Costa, ML de Oliveira, A Carrilho, H Villar, ... The Journal of Clinical Endocrinology & Metabolism 88 (12), 5739-5746, 2003 | 116 | 2003 |
| Management of ambiguous genitalia in pseudohermaphrodites: new perspectives on vaginal dilation EMF Costa, BB Mendonca, M Inácio, IJP Arnhold, FAQ Silva, O Lodovici Fertility and Sterility 67 (2), 229-232, 1997 | 108 | 1997 |
| Height and bone mineral density in androgen insensitivity syndrome with mutations in the androgen receptor gene DLS Danilovic, PHS Correa, EMF Costa, KFS Melo, BB Mendonca, ... Osteoporosis International 18, 369-374, 2007 | 104 | 2007 |
| Nonsense Mutations in FGF8 Gene Causing Different Degrees of Human Gonadotropin-Releasing Deficiency EB Trarbach, AP Abreu, LFG Silveira, HM Garmes, MTM Baptista, ... The Journal of Clinical Endocrinology & Metabolism 95 (7), 3491-3496, 2010 | 95 | 2010 |
| 46, XY disorder of sex development (DSD) due to 17β-hydroxysteroid dehydrogenase type 3 deficiency BB Mendonca, NL Gomes, EMF Costa, M Inacio, RM Martin, MY Nishi, ... The Journal of steroid biochemistry and molecular biology 165, 79-85, 2017 | 90 | 2017 |
| Wide spectrum of NR5A1‐related phenotypes in 46, XY and 46, XX individuals S Domenice, AZ Machado, FM Ferreira, B Ferraz‐de‐Souza, AM Lerario, ... Birth Defects Research Part C: Embryo Today: Reviews 108 (4), 309-320, 2016 | 90 | 2016 |
| Synthesis of naphthofuranquinones with activity against Trypanosoma cruzi RSF Silva, EM Costa, ÚLT Trindade, DV Teixeira, FR Maria de Carmo, ... European journal of medicinal chemistry 41 (4), 526-530, 2006 | 88 | 2006 |
