| Standard transition aluminas. Electron microscopy studies PS Santos, HS Santos, SP Toledo Materials Research 3, 104-114, 2000 | 1643 | 2000 |
| A HIF1α regulatory loop links hypoxia and mitochondrial signals in pheochromocytomas PLM Dahia, KN Ross, ME Wright, CY Hayashida, S Santagata, ... PLoS genetics 1 (1), e8, 2005 | 514 | 2005 |
| Germline mutations in TMEM127 confer susceptibility to pheochromocytoma Y Qin, L Yao, EE King, K Buddavarapu, RE Lenci, ES Chocron, ... Nature genetics 42 (3), 229-233, 2010 | 449 | 2010 |
| Clinical Characteristics and Therapeutic Responses in Patients with Germ-Line AIP Mutations and Pituitary Adenomas: An International Collaborative Study AF Daly, MA Tichomirowa, P Petrossians, E Heliovaara, ML Jaffrain-Rea, ... The Journal of Clinical Endocrinology & Metabolism 95 (11), E373-E383, 2010 | 396 | 2010 |
| Male pseudohermaphroditism due to a homozygous missense mutation of the luteinizing hormone receptor gene H Kremer, R Kraaij, SPA Toledo, M Post, JB Fridman, CY Hayashida, ... Nature genetics 9 (2), 160-164, 1995 | 396 | 1995 |
| Evaluation of gonadal function in 107 intersex patients by means of serum antimullerian hormone measurement RA Rey, C Belville, C Nihoul-Fékété, L Michel-Calemard, MG Forest, ... The Journal of Clinical Endocrinology & Metabolism 84 (2), 627-631, 1999 | 317 | 1999 |
| Familial dwarfism due to a novel mutation of the growth hormone-releasing hormone receptor gene R Salvatori, CY Hayashida, MH Aguiar-Oliveira, JA Phillips III, AHO Souza, ... The Journal of Clinical Endocrinology & Metabolism 84 (3), 917-923, 1999 | 291 | 1999 |
| Exomic Sequencing of Medullary Thyroid Cancer Reveals Dominant and Mutually Exclusive Oncogenic Mutations in RET and RAS N Agrawal, Y Jiao, M Sausen, R Leary, C Bettegowda, NJ Roberts, ... The Journal of Clinical Endocrinology & Metabolism 98 (2), E364-E369, 2013 | 270 | 2013 |
| An inactivating mutation of the luteinizing hormone receptor causes amenorrhea in a 46, XX female SP Toledo, HG Brunner, R Kraaij, M Post, PL Dahia, CY Hayashida, ... The Journal of Clinical Endocrinology & Metabolism 81 (11), 3850-3854, 1996 | 249 | 1996 |
| Spectrum and prevalence of FP/TMEM127 gene mutations in pheochromocytomas and paragangliomas L Yao, F Schiavi, A Cascon, Y Qin, L Inglada-Pérez, EE King, RA Toledo, ... Jama 304 (23), 2611-2619, 2010 | 235 | 2010 |
| Mutations in the RET proto-oncogene and the von Hippel-Lindau disease tumour suppressor gene in sporadic and syndromic phaeochromocytomas. C Eng, PA Crossey, LM Mulligan, CS Healey, C Houghton, A Prowse, ... Journal of Medical Genetics 32 (12), 934-937, 1995 | 226 | 1995 |
| Impaired adrenocorticotropin-adrenal axis in combined pituitary hormone deficiency caused by a two-base pair deletion (301–302delAG) in the prophet of Pit-1 gene F Pernasetti, SPA Toledo, VV Vasilyev, CY Hayashida, JD Cogan, ... The Journal of Clinical Endocrinology & Metabolism 85 (1), 390-397, 2000 | 189 | 2000 |
| Outcomes of adrenal-sparing surgery or total adrenalectomy in phaeochromocytoma associated with multiple endocrine neoplasia type 2: an international retrospective population … F Castinetti, XP Qi, MK Walz, AL Maia, G Sansó, M Peczkowska, ... The Lancet Oncology 15 (6), 648-655, 2014 | 175 | 2014 |
| The desmopressin stimulation test in the differential diagnosis of Cushing's syndrome DA Malerbi, BB Mendonça, B Liberman, SPA Toledo, MCM Corradini, ... Clinical endocrinology 38 (5), 463-472, 1993 | 165 | 1993 |
| Risk profiles and penetrance estimations in multiple endocrine neoplasia type 2A caused by germline RET mutations located in exon 10 K Frank‐Raue, LA Rybicki, Z Erlic, H Schweizer, A Winter, I Milos, ... Human mutation 32 (1), 51-58, 2011 | 158 | 2011 |
| Diverse growth hormone receptor gene mutations in Laron syndrome. MA Berg, J Argente, S Chernausek, R Gracia, J Guevara-Aguirre, M Hopp, ... American journal of human genetics 52 (5), 998, 1993 | 157 | 1993 |
| Hypercalcitoninemia is not pathognomonic of medullary thyroid carcinoma S Toledo, DM Lourenço Jr, MA Santos, MR Tavares, RA Toledo, ... Clinics 64, 699-706, 2009 | 144 | 2009 |
| A homozygous mutation in the luteinizing hormone receptor causes partial Leydig cell hypoplasia: correlation between receptor activity and phenotype JWM Martens, M Verhoef-Post, N Abelin, M Ezabella, SPA Toledo, ... Molecular Endocrinology 12 (6), 775-784, 1998 | 144 | 1998 |
| In vivo and in vitro oncogenic effects of HIF2A mutations in pheochromocytomas and paragangliomas RA Toledo, Y Qin, S Srikantan, NP Morales, Q Li, Y Deng, SW Kim, ... Endocrine-related cancer 20 (3), 349-359, 2013 | 139 | 2013 |
| Acheiropodia is caused by a genomic deletion in C7orf2, the human orthologue of the Lmbr1 gene P Ianakiev, MJ van Baren, MJ Daly, SPA Toledo, MG Cavalcanti, JC Neto, ... The American Journal of Human Genetics 68 (1), 38-45, 2001 | 118 | 2001 |
Delmar Muniz Lourenço JuniorProfessor Colaborador da FMUSP, Médico Assistente do HCFMUSP e ICESPVerified email at usp.br
