Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Tania Maria Barreto Rodrigues"'
Autor:
Tania Maria Barreto Rodrigues, Marlon Messias da Conceição Silva, Magali Maciel Freitas, Zélia Maria Costa Duarte, Vitória Sousa Frutuoso, Mariana Teixeira Rodrigues, Ileana Gabriela Sanchez Rubio
Publikováno v:
Frontiers in Endocrinology, Vol 12 (2021)
IntroductionIt is rare for a euthyroid mother to carry a child with a fetal goiter. However, cases of congenital hypothyroidism (CH) caused by thyroid dyshormonogenesis have been reported. Even though gene mutations associated with fetal goiter have
Externí odkaz:
https://doaj.org/article/06349c0a55034280ba69a34a709efa8d
Autor:
Sonir Roberto Rauber Antonini, Ana Claudia Latronico, Ana Pinheiro Machado Canton, Marina Cunha-Silva, Tania Maria Barreto Rodrigues, Berenice B. Mendonca, Carolina Ramos, Monica F Stecchini, Carlos Eduardo Seraphim, Delanie B. Macedo, Vinicius Nahime Brito
Publikováno v:
Neuroendocrinology. 110:705-713
Introduction: Loss-of-function mutation of MKRN3 represents the most frequent genetic cause of familial central precocious puberty (CPP). The outcomes of gonadotropin-releasing hormone analog (GnRHa) treatment in CPP patients with MKRN3 defects are u
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::827aeedd5bad78357239e6bbccae390b
https://doi.org/10.1159/000504446
https://doi.org/10.1159/000504446
Publikováno v:
Biblioteca Digital de Teses e Dissertações da UFMGUniversidade Federal de Minas GeraisUFMG.
A deficiência da enzima 21-hidroxilase é a causa mais frequente (90-95%) de Hiperplasia Adrenal Congênita (HAC), sendo caracterizada pela deficiência da secreção de cortisol e excesso de andrógenos. Na forma perdedora de sal, diagnosticada em
Externí odkaz:
http://hdl.handle.net/1843/BUOS-8UENNA