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Refinado por: Base de dados/Biblioteca: Oxford Journals - CRKN remover
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1
Mutations of the KISS1 Gene in Disorders of Puberty
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Artigo
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Mutations of the KISS1 Gene in Disorders of Puberty

Silveira, L. G ; Noel, S. D ; Silveira-Neto, A. P ; Abreu, A. P ; Brito, V. N ; Santos, M. G ; Bianco, S. D. C ; Kuohung, W ; Xu, S ; Gryngarten, M ; Escobar, M. E ; Arnhold, I. J. P ; Mendonca, B. B ; Kaiser, U. B ; Latronico, A. C

The journal of clinical endocrinology and metabolism, 2010-05, Vol.95 (5), p.2276-2280 [Periódico revisado por pares]

Bethesda, MD: Endocrine Society

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2
Spontaneous fertility in a male patient with testotoxicosis despite suppression of FSH levels
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Artigo
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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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3
Diagnostic value of fluorometric assays in the evaluation of precocious puberty
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Artigo
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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
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Artigo
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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
Longitudinal hormonal and pituitary imaging changes in two females with combined pituitary hormone deficiency due to deletion of A301,G302 in the PROP1 gene
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Artigo
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Longitudinal hormonal and pituitary imaging changes in two females with combined pituitary hormone deficiency due to deletion of A301,G302 in the PROP1 gene

MENDONCA, B. B ; OSORIO, M. G. F ; LATRONICO, A. C ; ESTEFAN, V ; SUH SIH LO, L ; ARNHOLD, I. J. P

The journal of clinical endocrinology and metabolism, 1999-03, Vol.84 (3), p.942-945 [Periódico revisado por pares]

Bethesda, MD: Endocrine Society

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6
Combined pituitary hormone deficiency caused by a novel mutation of a highly conserved residue (F88S) in the homeodomain of PROP-1
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Artigo
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Combined pituitary hormone deficiency caused by a novel mutation of a highly conserved residue (F88S) in the homeodomain of PROP-1

OSORIO, M. G. F ; KOPP, P ; MARUI, S ; LATRONICO, A. C ; MENDONCA, B. B ; ARNHOLD, I. J. P

The journal of clinical endocrinology and metabolism, 2000-08, Vol.85 (8), p.2779-2785 [Periódico revisado por pares]

Bethesda, MD: Endocrine Society

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7
A unique constitutively activating mutation in third transmembrane helix of luteinizing hormone receptor causes sporadic male gonadotropin-independent precocious puberty
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Artigo
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A unique constitutively activating mutation in third transmembrane helix of luteinizing hormone receptor causes sporadic male gonadotropin-independent precocious puberty

LATRONICO, A. C ; ABELL, A. N ; ARNHOLD, I. J. P ; LIU, X ; LINS, T. S. S ; BRITO, V. N ; BILLERBECK, A. E ; SEGALOFF, D. L ; MENDONCA, B. B

The journal of clinical endocrinology and metabolism, 1998-07, Vol.83 (7), p.2435-2440 [Periódico revisado por pares]

Bethesda, MD: Endocrine Society

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8
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
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Artigo
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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

Domenice, Sorahia ; Latronico, Ana Claudia ; Brito, Vinicius Nahime ; Arnhold, Ivo Jorge Prado ; Kok, Fernando ; Mendonca, Berenice Bilharinho

The journal of clinical endocrinology and metabolism, 2001-09, Vol.86 (9), p.4068-4071 [Periódico revisado por pares]

Bethesda, MD: Endocrine Society

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9
Molecular genotyping in Brazilian patients with the classical and nonclassical forms of 21-hydroxylase deficiency
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Artigo
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Molecular genotyping in Brazilian patients with the classical and nonclassical forms of 21-hydroxylase deficiency

BACHEGA, T. A. S. S ; BILLERBECK, A. E. C ; MADUREIRA, G ; MARCONDES, J. A. M ; LONGUI, C. A ; LEITE, M. V ; ARNHOLD, I. J. P ; MENDONCA, B. B

The journal of clinical endocrinology and metabolism, 1998-12, Vol.83 (12), p.4416-4419 [Periódico revisado por pares]

Bethesda, MD: Endocrine Society

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10
Mutations of the KISS1 Gene Associated with Central Precocious Puberty
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Artigo
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Mutations of the KISS1 Gene Associated with Central Precocious Puberty

Silveira, L. F. G ; Noel, S. D ; Silveira-Neto, A. P ; Abreu, A. P ; Brito, V. N ; Santos, M. AG ; Bianco, S. D. C ; Kuohung, W ; Xu, S ; Gryngarten, M ; Escobar, M. E ; Arnhold, I. J. P ; Mendonca, B. B ; Kaiser, U. B ; Latronico, A. C

Endocrine reviews, 2010-04, Vol.31 (2), p.255-255 [Periódico revisado por pares]

Endocrine Society

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