Reproductive outcome of women with 21-hydroxylase- deficient nonclassic adrenal hyperplasiaMORAN, C; AZZIZ, R; MENDONCA, B. B et al.The Journal of clinical endocrinology and metabolism. 2006, Vol 91, Num 9, pp 3451-3456, issn 0021-972X, 6 p.Article

Anti-corpus luteum antibody : A novel serological marker for ovarian dysfunction in systemic lupus erythematosus?PASOTO, S. G; VIANA, V. S. T; MENDONCA, B. B et al.Journal of rheumatology. 1999, Vol 26, Num 5, pp 1087-1093, issn 0315-162XArticle

17β-Hydroxysteroid dehydrogenase-3 deficiency: Diagnosis, phenotypic variability, population genetics, and worldwide distribution of ancient and de Novo mutationsBOEHMER, A. L. M; BRINKMANN, A. O; ROUWE, C. W et al.The Journal of clinical endocrinology and metabolism. 1999, Vol 84, Num 12, pp 4713-4721, issn 0021-972XArticle

A novel nonsense mutation in the first zinc finger of the vitamin D receptor causing hereditary 1,25-dihydroxyvitamin D₃-resistant ricketsMECHICA, J. B; LEITE, M. O. R; MENDONCA, B. B et al.The Journal of clinical endocrinology and metabolism. 1997, Vol 82, Num 11, pp 3892-3894, issn 0021-972XArticle

Ectopic adrenocorticotropic hormone syndromeWAJCHENBERG, B. L; MENDONCA, B. B; LIBERMAN, B et al.Endocrine reviews. 1994, Vol 15, Num 6, pp 752-787, issn 0163-769XArticle

Normal expression of the serologically defined H-Y antigen in Leydig cell hypoplasiaARNHOLD, I. J. P; MENDONCA, B. B; BISI, H et al.The Journal of urology. 1988, Vol 140, Num 6, pp 1549-1552, issn 0022-5347Article

Male pseudohermaphroditism due to nonsalt-losing 3β-hydroxysteroid dehydrogenase deficiency: gender role change and absence of gynecomastia at pubertyMENDONCA, B. B; BLOISE, W; PRADO ARNHOLD, I. J et al.Journal of steroid biochemistry. 1987, Vol 28, Num 6, pp 669-675, issn 0022-4731Article

Mutations of the KISS1 Gene in Disorders of PubertySILVEIRA, L. G; NOEL, S. D; ESCOBAR, M. E et al.The Journal of clinical endocrinology and metabolism. 2010, Vol 95, Num 5, pp 2276-2280, issn 0021-972X, 5 p.Article

Diagnostic value of fluorometric assays in the evaluation of precocious pubertyBRITO, V. N; BATISTA, M. C; BORGES, M. F et al.The Journal of clinical endocrinology and metabolism. 1999, Vol 84, Num 10, pp 3539-3544, issn 0021-972XArticle

Longitudinal hormonal and pituitary imaging changes in two females with combined pituitary hormone deficiency due to deletion of A301,G302 in the PROP1 geneMENDONCA, B. B; OSORIO, M. G. F; LATRONICO, A. C et al.The Journal of clinical endocrinology and metabolism. 1999, Vol 84, Num 3, pp 942-945, issn 0021-972XArticle

Low frequency of CYP21B deletions in Brazilian patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiencyBACHEGA, T. A. S. S; BILLERBECK, A. E. C; MADUREIRA, G et al.Human heredity. 1999, Vol 49, Num 1, pp 9-14, issn 0001-5652Article

Clinical features of women with resistance to luteinizing hormoneARNHOLD, I. J. P; LATRONICO, A. C; BATISTA, M. C et al.Clinical endocrinology (Oxford. Print). 1999, Vol 51, Num 6, pp 701-707, issn 0300-0664Article

A unique constitutively activating mutation in third transmembrane helix of luteinizing hormone receptor causes sporadic male gonadotropin-independent precocious pubertyLATRONICO, A. C; ABELL, A. N; ARNHOLD, I. J. P et al.The Journal of clinical endocrinology and metabolism. 1998, Vol 83, Num 7, pp 2435-2440, issn 0021-972XArticle

No evidence for oncogenic mutations in the adrenocorticotropin receptor gene in human adrenocortical neoplasmsLATRONICO, A. C; REINCKE, M; MENDONCA, B. B et al.The Journal of clinical endocrinology and metabolism. 1995, Vol 80, Num 3, pp 875-877, issn 0021-972XArticle

Adrenal autografts following bilateral adrenalectomyLUCON, A. M; MENDONCA, B. B; DOMENICE, S et al.The Journal of urology. 1993, Vol 149, Num 5, pp 977-979, issn 0022-5347Article

Origin of an ovarian steroid cell tumor causing isosexual pseudoprecocious puberty demonstrated by the expression of adrenal steroidogenic enzymes and adrenocorticotropin receptorLIN, C. J; JORGE, A. A. L; LATRONICO, A. C et al.The Journal of clinical endocrinology and metabolism. 2000, Vol 85, Num 3, pp 1211-1214, issn 0021-972XArticle

17β-hydroxysteroid dehydrogenase 3 deficiency in womenMENDONCA, B. B; ARNHOLD, I. J. P; BLOISE, W et al.The Journal of clinical endocrinology and metabolism. 1999, Vol 84, Num 2, pp 802-804, issn 0021-972XArticle

Treatment of gonadotropin dependent precocious puberty due to hypothalamic hamartoma with gonadotropin releasing hormone agonist depotDE BRITO, V. N; LATRONICO, A. C; ARNHOLD, I. J. P et al.Archives of disease in childhood. 1999, Vol 80, Num 3, pp 231-234, issn 0003-9888Article

A study of patients with Nelson's syndromeALBERGARIA PEREIRA, M. A; HALPERN, A; SALGADO, L. R et al.Clinical endocrinology (Oxford. Print). 1998, Vol 49, Num 4, pp 533-539, issn 0300-0664Article

Activating mutation of the stimulatory G protein (GSP) as a putative cause of ovarian and testicular human stromal Leydig cell tumorsVILLARES FRAGOSO, M. C. B; LATRONICO, A. C; CARVALHO, F. M et al.The Journal of clinical endocrinology and metabolism. 1998, Vol 83, Num 6, pp 2074-2078, issn 0021-972XArticle

Effects of acute and chronic zinc administration on growth velocity in patients with hypopituitarismESTEFAN, V; MENDONCA, B. B; ARNHOLD, I. J. P et al.Nutrition research (New York, NY). 1998, Vol 18, Num 11, pp 1865-1877, issn 0271-5317Article

Apparent mineralocorticoid excess in a Brazilian kindred : hypertension in the heterozygote stateLI, A; LI, K. X. Z; MARUI, S et al.Journal of hypertension. 1997, Vol 15, Num 12, pp 1397-1402, issn 0263-6352, 1Conference Paper

The effects of spironolactone on testosterone fractions and sex-hormone binding globulin binding capacity in hirsute womenMARCONDES, J. A. M; MINANNI, S. L; LUTHOLD, W. W et al.Journal of endocrinological investigation (Testo stampato). 1995, Vol 18, Num 6, pp 431-435, issn 0391-4097Article

Molecular genetics of steroid 5α-reductase 2 deficiencyTHIGPEN, A. E; DAVIS, D. L; MILATOVICH, A et al.The Journal of clinical investigation. 1992, Vol 90, Num 3, pp 799-809, issn 0021-9738Article

Molecular analysis of CYP21A2 can optimize the follow-up of positive results in newborn screening for congenital adrenal hyperplasiaSILVEIRA, E. L; ELNECAVE, R. H; DOS SANTOS, E. P et al.Clinical genetics. 2009, Vol 76, Num 6, pp 503-510, issn 0009-9163, 8 p.Article