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Spontaneous fertility in a male patient with testotoxicosis despite suppression of FSH levels
Spontaneous fertility in a male patient with testotoxicosis despite suppression of FSH levels
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Spontaneous fertility in a male patient with testotoxicosis despite suppression of FSH levels

Cunha-Silva, M ; Brito, V N ; Macedo, D B ; Bessa, D S ; Ramos, C O ; Lima, L G ; Barroso, P S ; Arnhold, I J P ; Segaloff, D L ; Mendonca, B B ; Latronico, A C

Human reproduction (Oxford), 2018-05, Vol.33 (5), p.914-918 [Periódico revisado por pares]

England: Oxford University Press

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2
Height and bone mineral density in androgen insensitivity syndrome with mutations in the androgen receptor gene
Height and bone mineral density in androgen insensitivity syndrome with mutations in the androgen receptor gene
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Height and bone mineral density in androgen insensitivity syndrome with mutations in the androgen receptor gene

DANILOVIC, D. L. S ; CORREA, P. H. S ; COSTA, E. M. F ; MELO, K. F. S ; MENDONCA, B. B ; ARNHOLD, I. J. P

Osteoporosis international, 2007-03, Vol.18 (3), p.369-374 [Periódico revisado por pares]

London: Springer

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3
Diagnostic value of fluorometric assays in the evaluation of precocious puberty
Diagnostic value of fluorometric assays in the evaluation of precocious puberty
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Diagnostic value of fluorometric assays in the evaluation of precocious puberty

BRITO, V. N ; BATISTA, M. C ; BORGES, M. F ; LATRONICO, A. C ; KOHEK, M. B. F ; THIRONE, A. C. P ; JORGE, B. H ; ARNHOLD, I. J. P ; MENDONCA, B. B

The journal of clinical endocrinology and metabolism, 1999-10, Vol.84 (10), p.3539-3544 [Periódico revisado por pares]

Bethesda, MD: Endocrine Society

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4
Two novel mutations in the gonadotropin-releasing hormone receptor gene in Brazilian patients with hypogonadotropic hypogonadism and normal olfaction
Two novel mutations in the gonadotropin-releasing hormone receptor gene in Brazilian patients with hypogonadotropic hypogonadism and normal olfaction
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Two novel mutations in the gonadotropin-releasing hormone receptor gene in Brazilian patients with hypogonadotropic hypogonadism and normal olfaction

Costa, E M ; Bedecarrats, G Y ; Mendonca, B B ; Arnhold, I J ; Kaiser, U B ; Latronico, A C

The journal of clinical endocrinology and metabolism, 2001-06, Vol.86 (6), p.2680-2686 [Periódico revisado por pares]

United States

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5
Influence of different genotypes on 17-hydroxyprogesterone levels in patients with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Influence of different genotypes on 17-hydroxyprogesterone levels in patients with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency
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Influence of different genotypes on 17-hydroxyprogesterone levels in patients with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Bachega, Tânia A. S. S. ; Billerbeck, Ana E. C. ; Marcondes, José A. M. ; Madureira, Guiomar ; Arnhold, Ivo J. P. ; Mendonca, Berenice B.

Clinical endocrinology (Oxford), 2000-05, Vol.52 (5), p.601-607 [Periódico revisado por pares]

Oxford BSL: Blackwell Science Ltd

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6
The effect of distinct activating mutations of the luteinizing hormone receptor gene on the pituitary-gonadal axis in both sexes
The effect of distinct activating mutations of the luteinizing hormone receptor gene on the pituitary-gonadal axis in both sexes
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The effect of distinct activating mutations of the luteinizing hormone receptor gene on the pituitary-gonadal axis in both sexes

Latronico, Ana Claudia ; Lins, Teresa Selma S. ; Brito, Vinicius Nahime ; Arnhold, Ivo Jorge P. ; Mendonca, Berenice B.

Clinical endocrinology (Oxford), 2000-11, Vol.53 (5), p.609-613 [Periódico revisado por pares]

Oxford BSL: Blackwell Science Ltd

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7
Management of ambiguous genitalia in pseudohermaphrodites: New perspectives on vaginal dilation
Management of ambiguous genitalia in pseudohermaphrodites: New perspectives on vaginal dilation
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Management of ambiguous genitalia in pseudohermaphrodites: New perspectives on vaginal dilation

Frade Costa, Elaine Maria ; Mendonca, Berenice Bilharinho ; Inácio, Marlene ; Prado Arnhold, Ivo Jorge ; Queiroz Silva, Frederico Antonio ; Lodovici, Orlando

Fertility and sterility, 1997-02, Vol.67 (2), p.229-232 [Periódico revisado por pares]

New York, NY: Elsevier Inc

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8
Apparent mineralocorticoid excess in a Brazilian kindred: hypertension in the heterozygote state
Apparent mineralocorticoid excess in a Brazilian kindred: hypertension in the heterozygote state
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Apparent mineralocorticoid excess in a Brazilian kindred: hypertension in the heterozygote state

Li, Airong ; Li, Kevin X.Z ; Marui, Suemi ; Krozowski, Zygmunt S ; Batista, Marcelo C ; Whorwood, Christopher B ; Arnhold, Ive J.P ; Shackleton, Cedric H.L ; Mendonca, Berenice B ; Stewart, Paul M

Journal of hypertension, 1997-12, Vol.15 (12), p.1397-1402 [Periódico revisado por pares]

Hagerstown, MD: Lippincott-Raven Publishers

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9
Consensus Statement on the Diagnosis and Treatment of Children with Idiopathic Short Stature: A Summary of the Growth Hormone Research Society, the Lawson Wilkins Pediatric Endocrine Society, and the European Society for Paediatric Endocrinology Workshop
Consensus Statement on the Diagnosis and Treatment of Children with Idiopathic Short Stature: A Summary of the Growth Hormone Research Society, the Lawson Wilkins Pediatric Endocrine Society, and the European Society for Paediatric Endocrinology Workshop
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Consensus Statement on the Diagnosis and Treatment of Children with Idiopathic Short Stature: A Summary of the Growth Hormone Research Society, the Lawson Wilkins Pediatric Endocrine Society, and the European Society for Paediatric Endocrinology Workshop

Cohen, P ; Rogol, A. D ; Deal, C. L ; Saenger, P ; Reiter, E. O ; Ross, J. L ; Chernausek, S. D ; Savage, M. O ; Wit, J. M

The Journal of clinical endocrinology and metabolism, 2008-11, Vol.93 (11), p.4210-4217 [Periódico revisado por pares]

Bethesda, MD: Endocrine Society

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10
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
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
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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

DOMENICE, S ; NISHI, M. Y ; BILHARINHO MENDONCA, B ; CORREIA BILLERBECK, A. E ; LATRONICO, A. C ; MEDEIROS, M. A ; RUSSELL, A. J ; VASS, K ; CARVALHO, F. M ; COSTA FRADE, E. M ; PRADO ARNHOLD, I. J

Human genetics, 1998-02, Vol.102 (2), p.213-215 [Periódico revisado por pares]

Heidelberg: Springer

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