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1 |
Material Type: Artigo
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Adrenocortical carcinoma : Clinical and laboratory observationsWAJCHENBERG, B. L ; ALBERGARIA PEREIRA, M. A ; MEDONCA, B. B ; LATRONICO, A. C ; CAMPOS CARNEIRO, P ; FERREIRA ALVES, V. A ; ZERBINI, M. C. N ; LIBERMAN, B ; GOMES, G. C ; KIRSCHNER, M. ACancer, 2000-02, Vol.88 (4), p.711-736 [Periódico revisado por pares]New York, NY: Wiley-LissTexto completo disponível |
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Material Type: Artigo
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Mutational Analysis of the Genes Encoding RFAmide-Related Peptide-3, the Human Orthologue of Gonadotrophin-Inhibitory Hormone, and its Receptor (GPR147) in Patients with Gonadotrophin-Releasing Hormone-Dependent Pubertal DisordersLima, C. J. G. ; Cardoso, S. C. ; Lemos, E. F. L. ; Zingler, E. ; Capanema, C. ; Menezes, L. D. ; Vogado, G. ; dos Santos, B. T. A. ; de Moraes, O. L. ; Duarte, E. F. ; de Brito, V. N. ; Latronico, A. C. ; Lofrano-Porto, A.Journal of neuroendocrinology, 2014-11, Vol.26 (11), p.817-824 [Periódico revisado por pares]United States: Blackwell Publishing LtdTexto completo disponível |
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Material Type: Artigo
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Expression of adrenocorticotrophic hormone receptor mRNA in human adrenocortical neoplasms: correlation with P450scc expressionReincke, Martin ; Beuschlein, Felix ; Latronico, Anna-Claudia ; Arlt, Wiebke ; Chrousos, George P. ; Allolio, BrunoClinical endocrinology (Oxford), 1997-05, Vol.46 (5), p.619-626 [Periódico revisado por pares]Oxford UK: Blackwell Science LtdTexto completo disponível |
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Material Type: Artigo
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The effect of distinct activating mutations of the luteinizing hormone receptor gene on the pituitary-gonadal axis in both sexesLatronico, 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 LtdTexto completo disponível |
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Material Type: Artigo
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Glucocorticoid receptor gene polymorphisms in ACTH-secreting pituitary tumoursAntonini, S. R. R. ; Latronico, A. C. ; Elias, L. L. K. ; Cukiert, A. ; Machado, H. R. ; Liberman, B. ; Mendonca, B. B. ; Moreira, A. C. ; Castro, M.Clinical endocrinology (Oxford), 2002-11, Vol.57 (5), p.657-662 [Periódico revisado por pares]Oxford, UK: Blackwell Science LtdTexto completo disponível |
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Material Type: Artigo
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Clinical features of women with resistance to luteinizing hormoneArnhold, Ivo J.P. ; Latronico, Ana C. ; Batista, Marcelo C. ; Izzo, Carlos R. ; Mendonca, Berenice B.Clinical endocrinology (Oxford), 1999-12, Vol.51 (6), p.701-707 [Periódico revisado por pares]Oxford BSL: Blackwell Science LtdTexto completo disponível |
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Material Type: Artigo
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Polymorphisms in the bovine follicle-stimulating hormone receptor geneRahal, P ; Latronico, A C ; Kohek, M B ; de Lucia, R F ; Milazzotto, M P ; Wheeler, M B ; Ferraz, J B ; Eler, J P ; Garcia, J FAnimal genetics, 2000-08, Vol.31 (4), p.280-281 [Periódico revisado por pares]England: Wiley Subscription Services, IncTexto completo disponível |
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Material Type: Artigo
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Mutations in the type II 3β-hydroxysteroid dehydrogenase (HSD3B2) gene can cause premature pubarche in girlsMARUI, S ; CASTRO, M ; LATRONICO, A. C ; ELIAS, L. L. K ; ARNHOLD, I. J. P ; MOREIRA, A. C ; MENDONCA, B. BClinical endocrinology (Oxford), 2000-01, Vol.52 (1), p.67-75 [Periódico revisado por pares]Oxford BSL: Blackwell Science LtdTexto completo disponível |
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Material Type: Artigo
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A novel point mutation (R840S) in the androgen receptor in a Brazilian family with partial androgen insensitivity syndromeMelo, Karla F.S. ; Latronico, Ana Claudia ; Costa, Elaine M.F. ; Billerbeck, Ana Elisa C. ; Mendonca, Berenice B. ; Arnhold, Ivo J.P.Human mutation, 1999-10, Vol.14 (4), p.353-353 [Periódico revisado por pares]New York: John Wiley & Sons, IncTexto completo disponível |
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Material Type: Artigo
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A novel homozygous nonsense mutations E135 in the type II 3beta-hydroxysteroid dehydrogenase gene in a girl with salt-losing congenital adrenal hyperplasia. Mutations in brief no. 168. OnlineMarui, S ; Torrealba, I M ; Russell, A J ; Latronico, A C ; Sutcliffe, R G ; Mendonca, B BHuman mutation, 1998, Vol.12 (2), p.139-139 [Periódico revisado por pares]United StatesTexto completo disponível |