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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
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Published in The journal of clinical endocrinology and metabolism (01.05.2010)
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Abrão, M. G., Leite, M. V., Carvalho, L. R., Billerbeck, A. E. C., Nishi, M. Y., Barbosa, A. S., Martin, R. M., Arnhold, I. J. P., Mendonca, B. B.
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Growth hormone pharmacogenetics: the interactive effect of a microsatellite in the IGF1 promoter region with the GHR-exon 3 and -202 A/C IGFBP3 variants on treatment outcomes of children with severe GH deficiency
Costalonga, E F, Antonini, S R R, Guerra, Jr, G, Coletta, R R D, Franca, M M, Braz, A F, Mendonca, B B, Arnhold, I J P, Jorge, A A L
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Molecular mechanisms of pituitary organogenesis: In search of novel regulatory genes
Davis, S.W., Castinetti, F., Carvalho, L.R., Ellsworth, B.S., Potok, M.A., Lyons, R.H., Brinkmeier, M.L., Raetzman, L.T., Carninci, P., Mortensen, A.H., Hayashizaki, Y., Arnhold, I.J.P., Mendonça, B.B., Brue, T., Camper, S.A.
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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
Published in Human reproduction (Oxford) (01.05.2018)
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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
Published in Endocrine reviews (01.04.2010)
Published in Endocrine reviews (01.04.2010)
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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
Published in Endocrinology (Philadelphia) (01.04.2010)
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Sleep characteristics of adolescents: A longitudinal study
Andrade, Miriam M.M., Benedito-Silva, Ana A., Domenice, Sorahia, Arnhold, Ivo J.P., Menna-Barreto, Luiz
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Treatment of gonadotropin dependent precocious puberty due to hypothalamic hamartoma with gonadotropin releasing hormone agonist depot
de Brito, Vinicius N, Latronico, Ana C, Arnhold, Ivo J P, Lo, Leonard S S, Domenice, Sorahia, Albano, Maria C C, Fragoso, Maria C B V, Mendonca, Berenice B
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Two Novel Mutations in the Gonadotropin-Releasing Hormone Receptor Gene in Brazilian Patients with Hypogonadotropic Hypogonadism and Normal Olfaction1
Costa, E. M. F, Bedecarrats, G. Y, Mendonca, B. B, Arnhold, I. J. P, Kaiser, U. B, Latronico, A. C
Published in The journal of clinical endocrinology and metabolism (01.06.2001)
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A clinico-genetic investigation of Leydig cell hypoplasia
Saldanha, P H, Arnhold, I J, Mendonça, B B, Bloise, W, Toledo, S P
Published in American journal of medical genetics (01.02.1987)
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Identification of nonclassical 21-hydroxylase deficiency in girls with precocious pubarche
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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
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Testicular and Ovarian Resistance to Luteinizing Hormone Caused by Inactivating Mutations of the Luteinizing Hormone–Receptor Gene
Latronico, Ana C, Anasti, James, Arnhold, Ivo J.P, Rapaport, Robert, Mendonca, Berenice B, Bloise, Walter, Castro, Margaret, Tsigos, Constantine, Chrousos, George P
Published in The New England journal of medicine (22.02.1996)
Published in The New England journal of medicine (22.02.1996)
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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
Published in The journal of clinical endocrinology and metabolism (01.10.1999)
Published in The journal of clinical endocrinology and metabolism (01.10.1999)
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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
Published in The journal of clinical endocrinology and metabolism (01.08.2000)
Published in The journal of clinical endocrinology and metabolism (01.08.2000)
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Mutation in 3ß-hydroxysteroid dehydrogenase type II associated with pseudohermaphroditism in males and premature pubarche or cryptic expression in females
Mendonça, B B, Russell, A J, Vasconcelos-Leite, M, Arnhold, IJ P, Bloise, W, Wajchenberg, B L, Nicolau, W, Sutcliffe, R G, Wallace, A M
Published in Journal of molecular endocrinology (01.02.1994)
Published in Journal of molecular endocrinology (01.02.1994)
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Prepubertal male pseudohermaphroditism due to 17-ketosteroid reductase deficiency: diagnostic value of a hCG test and lack of HLA association
Arnhold, I J, Mendonça, B B, Diaz, J A, Nogueira, C, Batista, M C, Madureira, G, Oliveira, D, Nicolau, W, Bloise, W
Published in Journal of endocrinological investigation (01.04.1988)
Published in Journal of endocrinological investigation (01.04.1988)
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