Berenice Bilharinho de Mendonça
Berenice Bilharinho de Mendonça
Faculdade de Medicina da Universidade de São Paulo
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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
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
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
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
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
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
Ectopic adrenocorticotropic hormone syndrome
BL Wajchenberg, BB Mendonca, B Liberman, MAA Pereira, PC Carneiro, ...
Endocrine reviews 15 (6), 752-787, 1994
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
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
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
Structure and Expression of a New Complementary DNA Encoding the almost Exclusive 3β-Hydroxysteroid Dehydrogenase/Δ54-lsomerase in Human Adrenals …
E Rhéaume, Y Lachance, HF Zhao, N Breton, M Dumont, Y Launoit, ...
Molecular endocrinology 5 (8), 1147-1157, 1991
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
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
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
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
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
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
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
Longitudinal hormonal and pituitary imaging changes in two females with combined pituitary hormone deficiency due to deletion of A301, G302 in the PROP1 gene
BB Mendonca, MGF Osorio, AC Latronico, V Estefan, LSS Lo, IJP Arnhold
The Journal of Clinical Endocrinology & Metabolism 84 (3), 942-945, 1999
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
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