Insulin resistence in congenital adrenal hyperplasia is compensated for by reduced insulin clearance

Autor: Oliveira, Daniel Minutti de, 1979

Publikováno v: Biblioteca Digital de Teses e Dissertações da Universidade Estadual de Campinas (UNICAMP)
Universidade Estadual de Campinas (UNICAMP)
instacron:UNICAMP

Orientadores: Bruno Geloneze Neto, Sofia Helena Valente de Lemos-Marini Tese (doutorado) - Universidade Estadual de Campinas, Faculdade de Ciências Médicas Resumo: Contexto: Pacientes com a forma clássica da hiperplasia adrenal congênita (HAC) t�

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3056::981ed9911e355a7d7d188cabdce52dd9

Long-term follow-up of an 8-year-old boy with insulinoma as the first manifestation of a familial form of multiple endocrine neoplasia type 1

Autor: Fabbri, Helena Campos, Mello, Maricilda Palandi de, Soardi, Fernanda Caroline, Esquiaveto-Aun, Adriana Mangue, Oliveira, Daniel Minutti de, Denardi, Fernanda Canova, Moura-Neto, Arnaldo, Garmes, Heraldo Mendes, Baptista, Maria Tereza Matias, Matos, Patrícia Sabino de, Lemos-Marini, Sofia Helena Valente de, D'Souza-Li, Lilia Freire Rodrigues, Guerra-Júnior, Gil

Publikováno v: Arquivos Brasileiros de Endocrinologia & Metabologia v.54 n.8 2010
Arquivos Brasileiros de Endocrinologia & Metabologia
Sociedade Brasileira de Endocrinologia e Metabologia (SBEM)
instacron:SBEM
Arquivos Brasileiros de Endocrinologia & Metabologia, Volume: 54, Issue: 8, Pages: 754-760, Published: NOV 2010

Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant hereditary cancer syndrome characterized mostly by parathyroid, enteropancreatic, and anterior pituitary tumors. We present a case of an 8-year-old boy referred because of hypoglycem

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::f94fb1d9d901a4dcf0179281a89067f4
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0004-27302010000800016

Six new cases confirm the clinical molecular profile of complete combined 17α-hydroxylase/ 17,20-lyase deficiency in Brazil

Autor: Belgini, Daiane Rodrigues Barbosa, Mello, Maricilda Palandi de, Baptista, Maria Tereza Matias, Oliveira, Daniel Minutti de, Denardi, Fernanda Canova, Garmes, Heraldo Mendes, Grassiotto, Oswaldo da Rocha, Benetti Pinto, Cristina Laguna, Marques-de-Faria, Antonia Paula, Maciel-Guerra, Andréa Trevas, Guerra-Júnior, Gil

Publikováno v: Arquivos Brasileiros de Endocrinologia & Metabologia, Volume: 54, Issue: 8, Pages: 711-716, Published: NOV 2010

In 2004, Costa-Santos and cols. reported 24 patients from 19 Brazilian families with 17α-hydroxylase deficiency and showed that p.W406R and p.R362C corresponded to 50% and 32% of CYP17A1 mutant alleles, respectively. The present report describes cli

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od_______608::1dd3a2dc68bef6bf27354ce2fde8c1ba
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-27302010000800008&lng=en&tlng=en

Six new cases confirm the clinical molecular profile of complete combined 17α-hydroxylase/ 17,20-lyase deficiency in Brazil.

Autor: Belgini DR; Center for Molecular Biology and Genetic Engineering, Universidade Estadual de Campinas, SP, Brazil., Mello MP, Baptista MT, Oliveira DM, Denardi FC, Garmes HM, Grassiotto Oda R, Benetti Pinto CL, Marques-de-Faria AP, Maciel-Guerra AT, Guerra-Júnior G

Publikováno v: Arquivos brasileiros de endocrinologia e metabologia [Arq Bras Endocrinol Metabol] 2010 Nov; Vol. 54 (8), pp. 711-6.