| Regulation of aromatase expression in estrogen-responsive breast and uterine disease: from bench to treatment SE Bulun, Z Lin, G Imir, S Amin, M Demura, B Yilmaz, R Martin, ... Pharmacological reviews 57 (3), 359-383, 2005 | 698 | 2005 |
| Diagnosis and management of pseudohypoparathyroidism and related disorders: first international Consensus Statement G Mantovani, M Bastepe, D Monk, L De Sanctis, S Thiele, A Usardi, ... Nature Reviews Endocrinology 14 (8), 476-500, 2018 | 277 | 2018 |
| An inherited mutation outside the highly conserved DNA-binding domain of the p53 tumor suppressor protein in children and adults with sporadic adrenocortical tumors AC Latronico, EM Pinto, S Domenice, MCBV Fragoso, RM Martin, ... The Journal of Clinical Endocrinology & Metabolism 86 (10), 4970-4973, 2001 | 248 | 2001 |
| Cushing’s Syndrome Secondary to Adrenocorticotropin-Independent Macronodular Adrenocortical Hyperplasia due to Activating Mutations of GNAS1 Gene MCBV Fragoso, S Domenice, AC Latronico, RM Martin, MAA Pereira, ... The Journal of Clinical Endocrinology & Metabolism 88 (5), 2147-2151, 2003 | 197 | 2003 |
| Aromatase excess in cancers of breast, endometrium and ovary SE Bulun, D Chen, M Lu, H Zhao, Y Cheng, M Demura, B Yilmaz, ... The Journal of steroid biochemistry and molecular biology 106 (1-5), 81-96, 2007 | 125 | 2007 |
| 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 | 122 | 2003 |
| Male pseudohermaphroditism due to 17β-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 | 122 | 2000 |
| 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 | 97 | 2017 |
| Bone quality and osteoporosis therapy RM Martin, PHS Correa Arquivos Brasileiros de Endocrinologia & Metabologia 54, 186-199, 2010 | 93 | 2010 |
| Regional rearrangements in chromosome 15q21 cause formation of cryptic promoters for the CYP19 (aromatase) gene M Demura, RM Martin, M Shozu, S Sebastian, K Takayama, WT Hsu, ... Human molecular genetics 16 (21), 2529-2541, 2007 | 80 | 2007 |
| An unusual phenotype of Frasier syndrome due to IVS9+ 4C> T mutation in the WT1 gene: predominantly male ambiguous genitalia and absence of gonadal dysgenesis KFS Melo, RM Martin, EMF Costa, FM Carvalho, AA Jorge, IJP Arnhold, ... The Journal of Clinical Endocrinology & Metabolism 87 (6), 2500-2505, 2002 | 80 | 2002 |
| Familial hyperestrogenism in both sexes: clinical, hormonal, and molecular studies of two siblings RM Martin, CJ Lin, MY Nishi, AEC Billerbeck, AC Latronico, DW Russell, ... The Journal of Clinical Endocrinology & Metabolism 88 (7), 3027-3034, 2003 | 71 | 2003 |
| Recommendations for diagnosis and treatment of pseudohypoparathyroidism and related disorders: an updated practical tool for physicians and patients G Mantovani, M Bastepe, D Monk, L De Sanctis, S Thiele, SF Ahmed, ... Hormone research in paediatrics 93 (3), 182-196, 2020 | 58 | 2020 |
| Successful live birth in a woman with 17α-hydroxylase deficiency through IVF frozen-thawed embryo transfer PHM Bianchi, GRFCA Gouveia, EMF Costa, S Domenice, RM Martin, ... The Journal of Clinical Endocrinology & Metabolism 101 (2), 345-348, 2016 | 56 | 2016 |
| Origin of an ovarian steroid cell tumor causing isosexual pseudoprecocious puberty demonstrated by the expression of adrenal steroidogenic enzymes and adrenocorticotropin receptor CJ Lin, AAL Jorge, AC Latronico, S Marui, MCV Fragoso, RM Martin, ... The Journal of Clinical Endocrinology & Metabolism 85 (3), 1211-1214, 2000 | 53 | 2000 |
| Combined pituitary hormone deficiency (CPHD) due to a complete PROP1 deletion MG Abrão, MV Leite, LR Carvalho, AEC Billerbeck, MY Nishi, AS Barbosa, ... Clinical endocrinology 65 (3), 294-300, 2006 | 42 | 2006 |
| Assessment of the role of transcript for GATA-4 as a marker of unfavorable outcome in human adrenocortical neoplasms AS Barbosa, LR Giacaglia, RM Martin, BB Mendonca, CJ Lin BMC endocrine disorders 4, 1-11, 2004 | 41 | 2004 |
| Evaluation of bone mineral density and microarchitectural parameters by DXA and HR-pQCT in 37 children and adults with X-linked hypophosphatemic rickets GP Colares Neto, RMR Pereira, JC Alvarenga, L Takayama, MFA Funari, ... Osteoporosis International 28, 1685-1692, 2017 | 40 | 2017 |
| Oral and maxillofacial manifestations of chronic kidney disease–mineral and bone disorder: a multicenter retrospective study FSC Pontes, MA Lopes, LL de Souza, DS da Mata Rezende, ... Oral surgery, oral medicine, oral pathology and oral radiology 125 (1), 31-43, 2018 | 35 | 2018 |
| Clinical, hormonal, ovarian, and genetic aspects of 46, XX patients with congenital adrenal hyperplasia due to CYP17A1 defects LC de Carvalho, VN Brito, RM Martin, AM Zamboni, LG Gomes, M Inácio, ... Fertility and Sterility 105 (6), 1612-1619, 2016 | 33 | 2016 |
