Repercussões materno-fetais da deficiência de vitamina D em mulheres com diabetes gestacional

Autor: Weinert, Letícia Schwerz

Publikováno v: Biblioteca Digital de Teses e Dissertações da UFRGSUniversidade Federal do Rio Grande do SulUFRGS.

O estudo das funções extra-esqueléticas da vitamina D vem ampliando-se nos últimos anos. Na gestação, a preocupação com os níveis de vitamina D maternos ocorre pela necessidade desta vitamina para a formação do esqueleto fetal e pela assoc

Externí odkaz: http://hdl.handle.net/10183/143430

Efficacy of empagliflozin for weight and glycemic control of a patient with Prader-Willi syndrome, systemic lymphedema and extreme obesity: a case report.

Autor: Farinha, Juliano Boufleur¹ juliano.farinha@ebserh.gov.br, Weinert, Letícia Schwerz¹, Costa, Lidiane Pozza¹, Costa, Marcelo Zanusso¹, de Peres, Patrícia Peres¹, Lorea, Cláudia Fernandes¹

Publikováno v: International Journal of Diabetes in Developing Countries. Oct2022, Vol. 42 Issue 4, p787-790. 4p.

Targeted sequencing identifies novel variants in common and rare MODY genes

Autor: Santana, Lucas Santos de, Caetano, Lílian Araújo, Riquetto, Aline Dantas Costa, Franco, Pedro Campos, Reis, André Fernandes, Weinert, Letícia Schwerz, Silveiro, Sandra Pinho, Vendramini, Marcio Faleiros, Prado, Flaviene Alves, Abrahão, Giovanna Campos Paranhos, Almeida, Ana Gregória Ferreira Pereira de, Tavares, Maria da Glória Rodrigues, Gonçalves, Wagner Rodrigo Brida, Santomauro Júnior, Augusto Cézar, Halpern, Bruno, Jorge, Alexander Augusto de Lima, Nery, Márcia, Bezerra, Milena Gurgel Teles

Publikováno v: Repositório Institucional da UFRGS
Universidade Federal do Rio Grande do Sul (UFRGS)
instacron:UFRGS

Background: Maturity-onset diabetes of the young (MODY) is a form of monogenic diabetes with autosomal dominant inheritance. To date, mutations in 11 genes have been frequently associated with this phenotype. In Brazil, few cohorts have been screened

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3056::46f281f60889a6bdd8df6b62f2e72de4

Vitamin D deficiency increases the risk of adverse neonatal otcomes in gestational diabetes

Autor: Weinert, Letícia Schwerz, Reichelt, Angela de Azevedo Jacob, Schmitt, Leonardo Rauber, Boff, Roberta, Oppermann, Maria Lúcia Rocha, Camargo, Joiza Lins, Silveiro, Sandra Pinho

Publikováno v: Repositório Institucional da UFRGS
Universidade Federal do Rio Grande do Sul (UFRGS)
instacron:UFRGS

Background: Gestational diabetes mellitus (GDM) and vitamin D deficiency have been associated with increased risk of adverse perinatal outcomes but the consequences of both conditions simultaneously present in pregnancy have not yet been evaluated. O

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3056::99cd2c98c165f174cf2e3c96ff845f0a

Qual o papel da mutação do TR β na carcinogênese da tireoide em humanos?

Autor: Weinert,Letícia Schwerz, Ceolin,Lucieli, Romitti,Mírian, Camargo,Eduardo Guimarães, Maia,Ana Luiza

Publikováno v: Arquivos Brasileiros de Endocrinologia & Metabologia, Volume: 56, Issue: 1, Pages: 67-71, Published: FEB 2012
Arquivos Brasileiros de Endocrinologia & Metabologia v.56 n.1 2012
Arquivos Brasileiros de Endocrinologia & Metabologia
Sociedade Brasileira de Endocrinologia e Metabologia (SBEM)
instacron:SBEM

Resistance to thyroid hormone (RTH) is a rare autosomal dominant inherited disorder characterized by end-organ reduced sensitivity to thyroid hormone. This syndrome is caused by mutations of the thyroid hormone receptor (TR) β gene, and its clinical

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::8a8c937102bde7d834c79db329561486
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-27302012000100010&lng=en&tlng=en