‪Berenice Bilharinho de Mendonça‬

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IVO ARNHOLDProfessor Livre Docente Endocrinologia, Faculdade de Medicina da Universidade de São PauloAdresse e-mail validée de usp.br
Ana Claudia LatronicoProfessora Titular da Endocrinologia, Departamento de Clínica Médica da Faculdade da USPAdresse e-mail validée de usp.br
Elaine Maria Frade CostaProfessora Livre Docente - Faculdade de Medicina da Universidade de São PauloAdresse e-mail validée de hcnet.usp.br
SORAHIA DOMENICEProfessora Assistente do Hospital das Clínicas da Faculdade de Medicina da USPAdresse e-mail validée de hcnet.usp.br
Alexander Augusto de Lima JorgeFaculdade de Medicina da Universidade de São Paulo - FMUSPAdresse e-mail validée de usp.br
Mirian Yumie NishiPesquisador Cientifico do Hospital das Clínicas da Faculdade de Medicina da Universidade de São PauloAdresse e-mail validée de usp.br
VINICIUS NAHIME DE BRITOUnidade de Endocrinologia do Desenvolvimento e Laboratório de Hormônios e Genética Molecular LIM 42Adresse e-mail validée de hc.fm.usp.br
Tania Aparecida Sartori Sanchez Bac...Professora Associada da Faculdade de Medicina da Universidade de São PauloAdresse e-mail validée de hcnet.usp.br
Luciani R CarvalhoHospital das Clínicas da Faculdade de Medicina de São PauloAdresse e-mail validée de usp.br
Antonio Marcondes LerarioUniversity of MichiganAdresse e-mail validée de umich.edu
Madson Queiroz AlmeidaProfessor Livre-Docente da Faculdade de Medicina da USPAdresse e-mail validée de usp.br
Luciana MontenegroPesqusiadora da Faculdade de Medicina da Universidade de São PauloAdresse e-mail validée de usp.br
Maria Cláudia Nogueira ZerbiniFacudade de Medicina-USPAdresse e-mail validée de usp.br
Leticia F Gontijo SilveiraProfessora Adjunta do Departamento de Clínica Médica da UFMGAdresse e-mail validée de ufmg.br
Bernardo Leo WajchenbergInstituto do Coração do H C FMUSPAdresse e-mail validée de incor.usp.br
Gil Guerra-JuniorUNICAMPAdresse e-mail validée de fcm.unicamp.br
Milena Gurgel TelesMédica Assistente da Disciplina de Endocrinologia e Metabologia, Faculdade de Medicina da Universidade de São PauloAdresse e-mail validée de usp.br
Carlos Alberto LonguiProfessor em Medicina, Faculdade de Ciencias Médicas da Santa Casa de São PauloAdresse e-mail validée de fcmsantacasasp.edu.br
Filomena Marino CarvalhoAssociate Professor, Department of Pathology, Faculdade de Medicina da Universidade de São PauloAdresse e-mail validée de usp.br
Sandra Mara Ferreira VillaresMédica Assistente do Hospital das Clínicas da FMUSPAdresse e-mail validée de hcnet.usp.br

Suivre

Berenice Bilharinho de Mendonça

Faculdade de Medicina da Universidade de São Paulo

Adresse e-mail validée de usp.br

Endocrinologia e Metabologia


Titre Trier par citations Trier par année Trier par titre	Citée par Citée par	Année
Male pseudohermaphroditism caused by mutations of testicular 17β–hydroxysteroid dehydrogenase 3 WM Geissler, DL Davis, L Wu, KD Bradshaw, S Patel, BB Mendonca, ... Nature genetics 7 (1), 34-39, 1994	735	1994
A GPR54-activating mutation in a patient with central precocious puberty MG Teles, SDC Bianco, VN Brito, EB Trarbach, W Kuohung, S Xu, ... New England Journal of Medicine 358 (7), 709-715, 2008	717	2008
Comprehensive pan-genomic characterization of adrenocortical carcinoma S Zheng, AD Cherniack, N Dewal, RA Moffitt, L Danilova, BA Murray, ... Cancer cell 29 (5), 723-736, 2016	695	2016
Central precocious puberty caused by mutations in the imprinted gene MKRN3 AP Abreu, A Dauber, DB Macedo, SD Noel, VN Brito, JC Gill, P Cukier, ... New England Journal of Medicine 368 (26), 2467-2475, 2013	588	2013
Mutant P450 oxidoreductase causes disordered steroidogenesis with and without Antley-Bixler syndrome CE Flück, T Tajima, AV Pandey, W Arlt, K Okuhara, CF Verge, EW Jabs, ... Nature genetics 36 (3), 228-230, 2004	541	2004
Molecular genetics of steroid 5 alpha-reductase 2 deficiency. AE Thigpen, DL Davis, A Milatovich, BB Mendonca, J Imperato-McGinley, ... The Journal of clinical investigation 90 (3), 799-809, 1992	491	1992
Testicular and ovarian resistance to luteinizing hormone caused by inactivating mutations of the luteinizing hormone–receptor gene AC Latronico, J Anasti, IJP Arnhold, R Rapaport, BB Mendonca, W Bloise, ... New England journal of medicine 334 (8), 507-512, 1996	445	1996
Mutations of the KISS1 Gene in Disorders of Puberty LG Silveira, SD Noel, AP Silveira-Neto, AP Abreu, VN Brito, MG Santos, ... The Journal of Clinical Endocrinology & Metabolism 95 (5), 2276-2280, 2010	428	2010
Ectopic adrenocorticotropic hormone syndrome BL Wajchenberg, BB Mendonca, B Liberman, MAA Pereira, PC Carneiro, ... Endocrine reviews 15 (6), 752-787, 1994	366	1994
The genetic and functional basis of isolated 17, 20–lyase deficiency DH Geller, RJ Auchus, BB Mendonça, WL Miller Nature genetics 17 (2), 201-205, 1997	347	1997
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	320	2010
The essential role of zinc in growth J Brandão-Neto, V Stefan, BB Mendonça, W Bloise, AVB Castro Nutrition research 15 (3), 335-358, 1995	317	1995
21-Hydroxylase–deficient nonclassic adrenal hyperplasia is a progressive disorder: A multicenter study C Moran, R Azziz, E Carmina, D Dewailly, F Fruzzetti, L Ibañez, ... American journal of obstetrics and gynecology 183 (6), 1468-1474, 2000	296	2000
Molecular genetics and pathophysiology of 17 beta-hydroxysteroid dehydrogenase 3 deficiency S Andersson, WM Geissler, L Wu, DL Davis, MM Grumbach, MI New, ... The Journal of Clinical Endocrinology & Metabolism 81 (1), 130-136, 1996	283	1996
The PROP1 2-base pair deletion is a common cause of combined pituitary hormone deficiency JD Cogan, W Wu, JA Phillips III, IJP Arnhold, A Agapito, OV Fofanova, ... The Journal of Clinical Endocrinology & Metabolism 83 (9), 3346-3349, 1998	265	1998
17β-hydroxysteroid dehydrogenase-3 deficiency: diagnosis, phenotypic variability, population genetics, and worldwide distribution of ancient and de novo mutations ALM Boehmer, AO Brinkmann, LA Sandkuijl, DJJ Halley, MF Niermeijer, ... The Journal of Clinical Endocrinology & Metabolism 84 (12), 4713-4721, 1999	261	1999
Reproductive outcome of women with 21-hydroxylase-deficient nonclassic adrenal hyperplasia C Moran, R Azziz, N Weintrob, SF Witchel, V Rohmer, D Dewailly, ... The Journal of Clinical Endocrinology & Metabolism 91 (9), 3451-3456, 2006	253	2006
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	251	2001
46, XY disorders of sex development (DSD) BB Mendonca, S Domenice, IJP Arnhold, EMF Costa Clinical endocrinology 70 (2), 173-187, 2009	248	2009
Diagnostic value of fluorometric assays in the evaluation of precocious puberty VN Brito, MC Batista, MF Borges, AC Latronico, MBF Kohek, ACP Thirone, ... The journal of Clinical endocrinology & metabolism 84 (10), 3539-3544, 1999	244	1999

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