Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Daniel Minutti de Oliveira"'
Autor:
Juliano Henrique Borges, Daniela Albiero Camargo, Leticia Esposito Sewaybricker, Renata Isa Santoro, Daniel Minutti de Oliveira, Sofia Helena Valente de Lemos-Marini, Bruno Geloneze, Gil Guerra-Júnior, Ezequiel Moreira Gonçalves
Publikováno v:
Archives of Endocrinology and Metabolism, Vol 67, Iss 1, Pp 64-72 (2022)
ABSTRACT Objective: Herein, we compared ambulatory blood pressure (ABP) between young adults with congenital adrenal hyperplasia (CAH) due to 21-hydroxylase enzyme (21OHase) deficiency and a control group. Additionally, we analyzed correlations betwe
Externí odkaz:
https://doaj.org/article/ab1e1fa4dcae4d69a5b177a31267b0b7
Autor:
Núbia Maria de Oliveira, Raquel David Langer, Sofia Helena Valente Lemos-Marini, Daniel Minutti de Oliveira, Bruno Geloneze, Gil Guerra-Júnior, Ezequiel Moreira Gonçalves
Publikováno v:
Nutrients, Vol 14, Iss 23, p 5184 (2022)
This study aimed to compare phase angle (PhA) and bioelectrical impedance vector analysis (BIVA) values between adult patients with congenital adrenal hyperplasia caused by 21-hydroxylase deficiency (CAH21OHD) and a control group. A total of 22 patie
Externí odkaz:
https://doaj.org/article/670bad2479024549a4a7337be78ae2eb
Autor:
Gil Guerra-Júnior, Bruno Geloneze, Ezequiel Moreira Gonçalves, Daniel Minutti de Oliveira, Juliano H. Borges, Sofia Helena Valente de Lemos-Marini
Publikováno v:
Osteoporosis International. 33:283-291
It is of great importance to investigate any potential detrimental effect on bone health in young adults with 21-hydroxylase enzyme deficiency undergoing glucocorticoid replacement therapy. This study demonstrated normal bone health in well-controlle
Autor:
Bruno Geloneze, Daniel Minutti de Oliveira, Sofia Helena Valente de Lemos-Marini, Juliano H. Borges, Gil Guerra-Júnior, Ezequiel Moreira Gonçalves
Publikováno v:
Lipids. 56:101-110
We aimed to compare detailed fat distribution and lipid profile between young adults with congenital adrenal hyperplasia due to 21-hydroxylase enzyme deficiency and a control group. We also verified independent associations of treatment duration and
Autor:
Ezequiel Moreira Gonçalves, Bruno Geloneze, Gil Guerra-Júnior, Juliano H. Borges, Sofia Helena Valente de Lemos-Marini, Renata Isa Santoro, Daniel Minutti de Oliveira
Publikováno v:
International journal of clinical practiceREFERENCES. 75(7)
Background The association of congenital adrenal hyperplasia (CAH) caused by 21-hydroxylase enzyme (21OHase) deficiency, duration of treatment and dosage with cardiovascular dysfunction in young adults remains unclear. We aimed to evaluate myocardial
Insulin Resistance in Congenital Adrenal Hyperplasia is Compensated for by Reduced Insulin Clearance
Autor:
Sofia Helena Valente de Lemos-Marini, Daniella Fernandes Camilo, Ana Carolina Junqueira Vasques, Daniel Minutti de Oliveira, Bruno Geloneze, Marcelo M O Lima, Gil Guerra-Júnior, Ezequiel Moreira Gonçalves, Andrea Tura
Publikováno v:
The Journal of clinical endocrinology and metabolism. 106(4)
Context Congenital adrenal hyperplasia (CAH) patients have potential normal longevity. However, a greater risk for cardiovascular disease has been reported. Insulin resistance and hyperinsulinemia have been described in CAH patients, whereas the prev
Autor:
Sofia Helena Valente de Lemos-Marini, Ana Carolina Junqueira Vasques, Bruno Geloneze, Ezequiel Moreira Gonçalves, Daniel Minutti de Oliveira, Gil Guerra-Júnior
Publikováno v:
Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists. 26(4)
Objective: To characterize resting energy expenditure (REE) in patients with classic 21-hydroxylase congenital adrenal hyperplasia (21-OH CAH) using indirect calorimetry and compare it to the most commonly used REE predictive equations. Methods: This
Autor:
Sofia Helena Valente de Lemos Marini, Renata Isa Santoro de Pieri, Ezequiel Moura Gonçalves, Daniella Fernandes Camilo, Ana Carolina Junqueira Vasques, Daniel Minutti de Oliveira, Bruno Geloneze Neto, Gil Guerra
Publikováno v:
Diabetology & Metabolic Syndrome
Autor:
Lília D'Souza-Li, Arnaldo Moura-Neto, Maricilda Palandi de Mello, Heraldo Mendes Garmes, Adriana Mangue Esquiaveto-Aun, Sofia Helena Valente de Lemos-Marini, Fernanda Canova Denardi, Maria Tereza Matias Baptista, Gil Guerra-Júnior, Daniel Minutti de Oliveira, Fernanda Caroline Soardi, Patrícia Sabino de Matos, Helena Campos Fabbri
Publikováno v:
Arquivos Brasileiros de Endocrinologia & Metabologia. 54:754-760
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
Autor:
Antonia Paula Marques-de-Faria, Daiane R.B. Belgini, Fernanda Canova Denardi, Heraldo Mendes Garmes, Maricilda Palandi de Mello, C.L.B. Pinto, Maria Tereza Matias Baptista, Daniel Minutti de Oliveira, Oswaldo da Rocha Grassiotto, Andréa Trevas Maciel-Guerra, Gil Guerra-Júnior
Publikováno v:
Arquivos brasileiros de endocrinologia e metabologia. 54(8)
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