Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Yanne Rocha Ramos"'
Autor:
Taíse Lima de Oliveira Cerqueira, Yanne Rocha Ramos, Giorgia Bruna Strappa, Mariana Souza de Jesus, Jailciele Gonzaga Santos, Camila Sousa, Gildásio Carvalho, Vladimir Fernandes, Ney Boa-Sorte, Tatiana Amorim, Thiago Magalhães Silva, Ana Marice Teixeira Ladeia, Angelina Xavier Acosta, Helton Estrela Ramos
Publikováno v:
Archives of Endocrinology and Metabolism, Vol 62, Iss 4, Pp 466-471
ABSTRACT Objective: To evaluate the candidate genes PAX-8, NKX2-5, TSH-R and HES-1 in 63 confirmed cases of thyroid dysgenesis. Subjects and methods: Characterization of patients with congenital hypothyroidism into specific subtypes of thyroid dysgen
Externí odkaz:
https://doaj.org/article/905a9e03dbd846cb9cd35b342a37189c
Autor:
Ana Marice Teixeira Ladeia, Jailciele Gonzaga, Taise Lima de Oliveira Cerqueira, Giorgia Strappa, Mariana Jesus, Daniel Lordelo San Martin, Anabel Costa, Vladimir Fernandes, Tatiana Amorim, Helton Estrela Ramos, Paulo Ferreira, Yanne Rocha Ramos
Publikováno v:
Archives of Endocrinology and Metabolism, Vol 59, Iss 6, Pp 562-567 (2015)
Objective To search for genetic alteration in NKX2.5 gene in patients presenting both congenital heart disease (CHD) and TD. Subjects and methods Individual phenotypes were carefully analyzed in 86 children with thyroid dysgenesis (TD) using thyroid
Autor:
Sara Cristina Lima Rebouças, Rebeca Beck, Leonardo S. G. Teixeira, Lorena Maia de Jesus, Taíse Lima de Oliveira Cerqueira, William Alves Santos, Renata de Oliveira Campos, Helton Estrela Ramos, Vanessa Cristina de Oliveira Souza, Tamires Xavier Marques, Yanne Rocha Ramos, Fernando Barbosa, Clotilde Assis Oliveira, Iasmin dos Santos Barreto
Publikováno v:
Thyroid : official journal of the American Thyroid Association. 26(7)
National programs of salt iodization were implemented in Brazil to combat iodine deficiency (ID) in children of school age. Currently, there are limited data in Brazil on those still vulnerable to this deficiency and the state of nutritional iodine s
Autor:
Camila Santana de Sousa, Ana Marice Teixeira Ladeia, Jailciele Gonzaga dos Santos, Thiago Magalhães da Silva, Tatiana Amorim, Yanne Rocha Ramos, Helton Estrela Ramos, Taise Lima de Oliveira Cerqueira, Angelina Xavier Acosta, G. M. C. Carvalho, Vladimir Fernandes, Mariana Souza de Jesus, Ney Boa-Sorte, Giorgia Strappa
Publikováno v:
Archives of Endocrinology and Metabolism, Vol 62, Iss 4, Pp 466-471
Archives of Endocrinology and Metabolism, Volume: 62, Issue: 4, Pages: 466-471, Published: AUG 2018
Archives of Endocrinology and Metabolism v.62 n.4 2018
Arquivos de Endocrinologia e Metabolismo
Sociedade Brasileira de Endocrinologia e Metabologia (SBEM)
instacron:SBEM
Archives of Endocrinology and Metabolism, Volume: 62, Issue: 4, Pages: 466-471, Published: AUG 2018
Archives of Endocrinology and Metabolism v.62 n.4 2018
Arquivos de Endocrinologia e Metabolismo
Sociedade Brasileira de Endocrinologia e Metabologia (SBEM)
instacron:SBEM
Objective: To evaluate the candidate genes PAX-8, NKX2-5, TSH-R and HES-1 in 63 confirmed cases of thyroid dysgenesis. Subjects and methods: Characterization of patients with congenital hypothyroidism into specific subtypes of thyroid dysgenesis with