Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Ana Claudia Latronico"'
Autor:
Marilza Leal Nascimento, Guiomar Madureira, Berenice B. Mendonca, Delanie B. Macedo, Ana Claudia Latronico, Carolina Ramos, Vinicius Nahime Brito, Tania A. S. S. Bachega
Publikováno v:
Hormone Research in Paediatrics. 91:411-415
Background/Aims: Premature pubarche is associated with conditions such as virilizing congenital adrenal hyperplasia, androgen-secreting tumors, and exogenous exposure to androgen products. We describe the clinical and hormonal features of a series of
Autor:
Berenice B. Mendonca, José I Labarta, Leandro Soriano-Guillén, Anna Flavia Figueiredo Benedetti, Lourdes Travieso-Suárez, Sonir Roberto Rauber Antonini, Ana Paula Abreu, Andrea de Castro Leal, Raquel Corripio, Priscila Gagliardi, Ana Claudia Latronico, Mirta Gryngarten, Maiara Ribeiro Piovesan, Luciana Ribeiro Montenegro, Andrea Arcari, Vinicius Nahime Brito, Jesús Argente, Ana Pinheiro Machado Canton, Nelmar Valentina Ortiz-Cabrera, Marina Cunha, Ursula B. Kaiser, Delanie B Macedo, Carolina Ramos, Arancha Escribano-Muñoz, Aline Guimaraes, Carlos Eduardo Seraphim
Publikováno v:
J Clin Endocrinol Metab
Context Loss-of-function mutations of makorin RING finger protein 3 (MKRN3) are the most common monogenic cause of familial central precocious puberty (CPP). Objective To describe the clinical and hormonal features of a large cohort of patients with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc2ac84958412f0da28ca2f0025f8938
https://europepmc.org/articles/PMC7993586/
https://europepmc.org/articles/PMC7993586/
Autor:
Deborah L. Segaloff, I J P Arnhold, Delanie B. Macedo, Priscila Sales Barroso, Danielle S Bessa, Vinicius Nahime Brito, Carolina Ramos, Ana Claudia Latronico, L G Lima, Berenice B. Mendonca, Marina Cunha-Silva
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
Testotoxicosis is a rare cause of peripheral precocious puberty in boys caused by constitutively activating mutations of the LHCG receptor. Affected males usually have normal gonadotropin profiles and fertility in their adult life. Here, we described
Autor:
Danielle S Bessa, Tais A S Menk, Delanie B. Macedo, Marlene Inácio, Berenice B. Mendonca, Ana Claudia Latronico, Vinicius Nahime Brito
Publikováno v:
Journal of Pediatric Endocrinology and Metabolism. 30:657-662
Background: The objective of the study was to determine the stress levels of girls with central precocious puberty (CPP) before and during treatment with a long-acting gonadotropin-releasing hormone agonist (GnRHa). Methods: The Child Stress Scale (C
Autor:
Juan Carlos Roa, Ursula B. Kaiser, Leonor Pinilla, Susana Sangiao-Alvarellos, Ana Claudia Latronico, Maria Manfredi-Lozano, Violeta Heras, Francisco Gaytan, Vincent Prevot, Juan M. Castellano, Ana Paula Abreu, Denise D. Belsham, Manuel Tena-Sempere, Maribel Lara-Chica, Marco A. Calzado, Rosario Morrugares-Carmona, María J. Sanchez-Tapia, María Jesús Vázquez, Francisco Ruiz-Pino, Nathalie Jouy
Publikováno v:
PLoS Biology
PLoS Biology, Public Library of Science, 2019, 17 (11), pp.e3000532. ⟨10.1371/journal.pbio.3000532⟩
PLoS Biology, 2019, 17 (11), pp.e3000532. ⟨10.1371/journal.pbio.3000532⟩
RUC. Repositorio da Universidade da Coruña
instname
PLoS Biology, Vol 17, Iss 11, p e3000532 (2019)
PLoS Biology, Public Library of Science, 2019, 17 (11), pp.e3000532. ⟨10.1371/journal.pbio.3000532⟩
PLoS Biology, 2019, 17 (11), pp.e3000532. ⟨10.1371/journal.pbio.3000532⟩
RUC. Repositorio da Universidade da Coruña
instname
PLoS Biology, Vol 17, Iss 11, p e3000532 (2019)
Mkrn3, the maternally imprinted gene encoding the makorin RING-finger protein-3, has recently emerged as putative pubertal repressor, as evidenced by central precocity caused by MKRN3 mutations in humans; yet, the molecular underpinnings of this key
Publikováno v:
Advanced Practice in Endocrinology Nursing ISBN: 9783319998152
This chapter will focus on two genetic syndromes affecting gonadotropin function that typically present in childhood, Klinefelter syndrome, and testotoxicosis.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7a5d87c6119004090fd8772296daf858
https://doi.org/10.1007/978-3-319-99817-6_10
https://doi.org/10.1007/978-3-319-99817-6_10
Autor:
Deborah L. Segaloff, George P. Chrousos, Q. R. Fan, Amalia Sertedaki, L. G. Silveira, Evangelia Charmandari, Ana Claudia Latronico, Meilin Zhang, Rongbin Guan
Publikováno v:
Molecular Endocrinology. 30:62-76
We demonstrate 2 novel mutations of the LHCGR, each homozygous, in a 46,XY patient with severe Leydig cell hypoplasia. One is a mutation in the signal peptide (p.Gln18_Leu19ins9; referred to here as SP) that results in an alteration of the coding seq
Autor:
Berenice B. Mendonca, Ivo J.P. Arnhold, Ana Claudia Latronico, Margaret de Castro, Madson Q. Almeida, Vinicius Nahime Brito, Gil Guerra-Júnior, Thereza Selma S. Lins, Sonir Roberto Rauber Antonini
Publikováno v:
Clinical Endocrinology. 69:93-98
Summary Background Familial male-limited precocious puberty (FMPP) or testotoxicosis is a rare gonadotrophin-independent form of sexual precocity caused by constitutively activating mutations of the LH receptor. Several clinical therapeutic approache
Autor:
Berenice B. Mendonca, Ana Claudia Latronico, Sorahia Domenice, I J P Arnhold, Maria Beatriz da Fonte Kohek, Elaine Maria Frade Costa, Rafaela Vieira Correa
Publikováno v:
Brazilian Journal of Medical and Biological Research, Vol 37, Iss 1, Pp 137-144 (2004)
Scopus-Elsevier
Brazilian Journal of Medical and Biological Research, Volume: 37, Issue: 1, Pages: 137-144, Published: JAN 2004
Brazilian Journal of Medical and Biological Research v.37 n.1 2004
Brazilian Journal of Medical and Biological Research
Associação Brasileira de Divulgação Científica (ABDC)
instacron:ABDC
Scopus-Elsevier
Brazilian Journal of Medical and Biological Research, Volume: 37, Issue: 1, Pages: 137-144, Published: JAN 2004
Brazilian Journal of Medical and Biological Research v.37 n.1 2004
Brazilian Journal of Medical and Biological Research
Associação Brasileira de Divulgação Científica (ABDC)
instacron:ABDC
Several genes that influence the development and function of the hypothalamic-pituitary-gonadal-axis (HPG) have been identified. These genes encode an array of transcription factors, matrix proteins, hormones, receptors, and enzymes that are expresse
Autor:
Berenice B. Mendonca, Lucila Leico Kagohara Elias, Ana Claudia Latronico, George P. Chrousos, Tomoshige Kino, Maristela V. Leite, Margaret de Castro, Ivo J.P. Arnhold, Tania A. S. S. Bachega
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 87:1805-1809
Familial glucocorticoid resistance is characterized by increased cortisol secretion without clinical evidence of hypercortisolism, but with manifestations of androgen and mineralocorticoid excess. This condition is mainly caused by mutations of the G