Mutations of the KISS1 Gene in Disorders of Puberty von 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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Combined pituitary hormone deficiency (CPHD) due to a complete PROP1 deletion von 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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Height and bone mineral density in androgen insensitivity syndrome with mutations in the androgen receptor gene von DANILOVIC, D. L. S, CORREA, P. H. S, COSTA, E. M. F, MELO, K. F. S, MENDONCA, B. B, ARNHOLD, I. J. P

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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 ch... von Costalonga, E F, Antonini, S R R, Guerra-Junior, 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 von 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 von 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

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Mutations of the KISS1 Gene Associated with Central Precocious Puberty von 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

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Mutations of the KISS1 Gene Associated with Central Precocious Puberty von 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

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Sleep characteristics of adolescents: A longitudinal study von 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 von 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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Testicular and Ovarian Resistance to Luteinizing Hormone Caused by Inactivating Mutations of the Luteinizing Hormone–Receptor Gene von Latronico, Ana C, Anasti, James, Arnhold, Ivo J.P, Rapaport, Robert, Mendonca, Berenice B, Bloise, Walter, Castro, Margaret, Tsigos, Constantine, Chrousos, George P

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

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

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Mutations in the SRY, DAX1, SF1 and WNT4 genes in Brazilian sex-reversed patients von Domenice, S, Corrêa, R V, Costa, E M F, Nishi, M Y, Vilain, E, Arnhold, I J P, Mendonca, B B

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

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Influence of different genotypes on 17-hydroxyprogesterone levels in patients with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency von Bachega, Tânia A. S. S., Billerbeck, Ana E. C., Marcondes, José A. M., Madureira, Guiomar, Arnhold, Ivo J. P., Mendonca, Berenice B.

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

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Mutations in the Type II 3β-Hydroxysteroid Dehydrogenase (HSD3B2) Gene Can Cause Premature Pubarche in Girls von Marui, S, Castro, M, Latronico, A C, Elias, L L. K, Arnhold, I J. P, Moreira, A C, Mendonca, B B

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

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Origin of an Ovarian Steroid Cell Tumor Causing Isosexual Pseudoprecocious Puberty Demonstrated by the Expression of Adrenal Steroidogenic Enzymes and Adrenocorticotropin Receptor von Lin, Chin J., Jorge, Alexander A. L., Latronico, Ana Claudia, Marui, Suemi, Fragoso, Maria Candida V., Martin, Regina M., Carvalho, Filomena M., Arnhold, Ivo J. P., Mendonca, Berenice B.

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