Výsledky vyhledávání - "Tania Maria Barreto Rodrigues"

Akademický článek

Case Report: Functional Analysis and Neuropsychological Evaluation of Dyshormonogenetic Fetal Goiter in Siblings Caused by Novel Compound Hyterozygous TPO Gene Mutations

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

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Dissertation/ Thesis

Identificação de fatores de risco cardiovascular e avaliação da espessura mediointimal das artérias carótidas em jovens e crianças com deficiência da enzima 21-hidroxilase

Autor: Tania Maria Barreto Rodrigues

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

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Outcomes of Patients with Central Precocious Puberty Due to Loss-of-Function Mutations in the MKRN3 Gene after Treatment with Gonadotropin-Releasing Hormone Analog

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

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Akademický článek

Cardiovascular risk factors and increased carotid intima-media thickness in young patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Autor: Tânia Maria Barreto Rodrigues, Cristina Botelho Barra, Jovita Lane Soares Santos, Eugênio Marcos Andrade Goulart, Adaliene Versiani Matos Ferreira, Ivani Novato Silva

Publikováno v: Archives of Endocrinology and Metabolism, Vol 59, Iss 6, Pp 541-547

ABSTRACT Objective Increased arterial intima-media thickness has been observed in adults with congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency (21-OHD). CAH has also been associated with obesity, insulin resistance, and hypertens

Externí odkaz: https://doaj.org/article/e2b5553322454e54bd5eb82747f13e89

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Akademický článek

INTIMA-MEDIA THICKNESS OF THE CAROTID ARTERIES IS AFFECTED BY PUBERTAL MATURATION IN HEALTHY ADOLESCENTS

Autor: Jovita Lane Soares Santos Zanini, Tânia Maria Barreto Rodrigues, Cristina Botelho Barra, Maria Francisca Tereza Freire Filgueiras, Ivani Novato Silva

Publikováno v: Revista Paulista de Pediatria

ABSTRACT Objective: To contribute to the assessment of normal parameters of carotid intima-media thickness (CIMT) in healthy adolescents. Methods: A cross-sectional study was conducted through clinical, laboratory and ultrasound evaluation in 61 heal

Externí odkaz: https://doaj.org/article/a6411b8ca77d4a169bd4072f3bd04e14

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