Professora Assistente do Hospital das Clínicas da Faculdade de Medicina da USP
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Sleep characteristics of adolescents: a longitudinal study
MMM Andrade, AA Benedito-Silva, S Domenice, IJP Arnhold, ...
Journal of Adolescent Health 14 (5), 401-406, 1993
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
46, XY disorders of sex development (DSD)
BB Mendonca, S Domenice, IJP Arnhold, EMF Costa
Clinical endocrinology 70 (2), 173-187, 2009
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
A microdeletion in the ligand binding domain of human steroidogenic factor 1 causes XY sex reversal without adrenal insufficiency
RV Correa, S Domenice, NC Bingham, AEC Billerbeck, WE Rainey, ...
The Journal of Clinical Endocrinology & Metabolism 89 (4), 1767-1772, 2004
Ectopic ACTH syndrome: our experience with 25 cases
LR Salgado, MCBV Fragoso, M Knoepfelmacher, MC Machado, ...
European Journal of Endocrinology 155 (5), 725-733, 2006
A novel mutation of the luteinizing hormone receptor gene causing male gonadotropin-independent precocious puberty
AC Latronico, J Anasti, IJ Arnhold, BB Mendonca, S Domenice, ...
The Journal of Clinical Endocrinology & Metabolism 80 (8), 2490-2494, 1995
Clinical, hormonal and pathological findings in a comparative study of adrenocortical neoplasms in childhood and adulthood
BB Mendonca, AM Lucon, CAV Menezes, LB Saldanha, AC Latronico, ...
The Journal of urology 154 (6), 2004-2009, 1995
Founder effect for the highly prevalent R337H mutation of tumor suppressor p53 in Brazilian patients with adrenocortical tumors
EM Pinto, AEC Billerbeck, MCBF Villares, S Domenice, BB Mendonça, ...
Arquivos Brasileiros de Endocrinologia & Metabologia 48 (5), 647-650, 2004
Adrenocorticotropin-dependent precocious puberty of testicular origin in a boy with X-linked adrenal hypoplasia congenita due to a novel mutation in the DAX1 gene
S Domenice, AC Latronico, VN Brito, IJP Arnhold, F Kok, BB Mendonca
The Journal of Clinical Endocrinology & Metabolism 86 (9), 4068-4071, 2001
Mutations in the SRY, DAX1, SF1 and WNT4 genes in Brazilian sex-reversed patients
S Domenice, RV Correa, EMF Costa, MY Nishi, E Vilain, IJP Arnhold, ...
Brazilian journal of medical and biological research 37 (1), 145-150, 2004
A novel missense mutation (S18N) in the 5′ non-HMG box region of the SRY gene in a patient with partial gonadal dysgenesis and his normal male relatives
S Domenice, MY Nishi, AEC Billerbeck, AC Latronico, MA Medeiros, ...
Human genetics 102 (2), 213-215, 1998
The role of desmopressin in bilateral and simultaneous inferior petrosal sinus sampling for differential diagnosis of ACTH‐dependent Cushing's syndrome
MC Machado, SV De Sa, S Domenice, MCBV Fragoso, P Puglia Jr, ...
Clinical endocrinology 66 (1), 136-142, 2007
Detection of Y‐specific sequences in 122 patients with Turner syndrome: Nested PCR is not a reliable method
MY Nishi, S Domenice, MA Medeiros, BB Mendonca, AEC Billerbeck
American journal of medical genetics 107 (4), 299-305, 2002
Disorders of sex development: effect of molecular diagnostics
JC Achermann, S Domenice, TASS Bachega, MY Nishi, BB Mendonca
Nature Reviews Endocrinology 11 (8), 478, 2015
Treatment of gonadotropin dependent precocious puberty due to hypothalamic hamartoma with gonadotropin releasing hormone agonist depot
VN de Brito, AC Latronico, IJP Arnhold, LSS Lo, S Domenice, ...
Archives of disease in childhood 80 (3), 231-234, 1999
Quality of life of patients with 46, XX and 46, XY disorders of sex development
RC Amaral, M Inacio, VN Brito, TASS Bachega, S Domenice, IJP Arnhold, ...
Clinical endocrinology 82 (2), 159-164, 2015
Human semaphorin 6B [(HSA) SEMA6B], a novel human class 6 semaphorin gene: alternative splicing and all-trans-retinoic acid-dependent downregulation in glioblastoma cell lines
RG Correa, RM Sasahara, MH Bengtson, MLH Katayama, ACM Salim, ...
Genomics 73 (3), 343-348, 2001
DSD due to 5α-reductase 2 deficiency-from diagnosis to long term outcome
EMF Costa, S Domenice, MH Sircili, M Inacio, BB Mendonca
Seminars in reproductive medicine 30 (05), 427-431, 2012
46, XY DSD due to impaired androgen production
BB Mendonca, EMF Costa, A Belgorosky, MA Rivarola, S Domenice
Best Practice & Research Clinical Endocrinology & Metabolism 24 (2), 243-262, 2010
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