Gilvan Cortes Nascimento
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Explore the profile of Gilvan Cortes Nascimento including associated specialties, affiliations and a list of published articles.
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11
Citations
80
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Recent Articles
1.
de Abreu J, Azulay R, Rodrigues V, de Abreu S, da Gloria Tavares M, Pinheiro F, et al.
Biomedicines
. 2024 Nov;
12(11).
PMID: 39595107
Background/objectives: Approximately 25% of the world's population and more than 60% of patients with type 2 diabetes (T2D) have metabolic-dysfunction-associated steatotic liver disease (MASLD). The association between these pathologies is...
2.
Azulay R, Rodrigues V, Lago D, Almeida A, de Abreu J, Matos L, et al.
Int J Mol Sci
. 2024 Oct;
25(20).
PMID: 39456927
Type 1 diabetes (T1D) is a chronic disease characterized by the immune-mediated destruction of the pancreatic beta cells responsible for insulin production. The secreted insulin and C-peptide are equimolar. Due...
3.
de Oliveira Neto C, de Sousa Azulay R, Almeida A, Tavares M, Vaz L, Leal I, et al.
Int J Environ Res Public Health
. 2022 Apr;
19(8).
PMID: 35457600
In the COVID-19 pandemic, there was an increase in consultations for precocious puberty. We aim to analyze differences in female puberty before and during the COVID-19 pandemic. A cross-sectional analytical...
4.
Reis R, de Sousa Azulay R, da Gloria Tavares M, Nascimento G, Damianse S, Rocha V, et al.
Genes (Basel)
. 2022 Feb;
13(2).
PMID: 35205433
Patients with type 1 diabetes (T1D) have a higher risk of developing cardiovascular disease (CVD), which is a major cause of death in this population. This study investigates early markers...
5.
de Sousa Azulay R, Porto L, Silva D, da Gloria Tavares M, Reis R, Nascimento G, et al.
Sci Rep
. 2021 Jul;
11(1):14157.
PMID: 34239025
This study aimed to investigate the relationship between genetic ancestry inferred from autosomal and Y chromosome markers and HLA genotypes in patients with Type 1 Diabetes from an admixed Brazilian...
6.
de Sousa Azulay R, Magalhaes M, da Gloria Tavares M, Dualibe R, Barbosa L, Sa Gaspar S, et al.
Am J Case Rep
. 2020 Apr;
21:e923108.
PMID: 32327622
BACKGROUND Juvenile hemochromatosis is a rare genetic disease that leads to intense iron accumulation. The disease onset usually occurs before the third decade of life and causes severe dysfunction in...
7.
Portovedo S, Gaido N, de Almeida Nunes B, Nascimento A, Rocha A, Magalhaes M, et al.
Mol Cell Endocrinol
. 2019 Apr;
490:80-87.
PMID: 30999005
Defining biomarkers for invasive pituitary neuroendocrine tumors (PitNETs) is highly desirable. The high mobility group A (HMGA) proteins are among the most widely expressed cancer-associated proteins. Indeed, their overexpression is...
8.
GuimaraesSa A, Ferreira P, Souza M, Nascimento G, Damianse S, Rocha V, et al.
Int J Endocrinol
. 2018 Apr;
2018:6135080.
PMID: 29681935
Objective: To identify the factors associated with quality of life in patients with acromegaly with follow-up at the referral service in neuroendocrinology of the state of Maranhão, northeast Brazil. Methods:...
9.
Vilar L, Fleseriu M, Naves L, Albuquerque J, Gadelha P, Faria M, et al.
Endocrine
. 2013 Nov;
46(3):577-84.
PMID: 24272601
Somatostatin analogs (SSAs) represent the mainstay of therapy in acromegaly. One of the potential disadvantages is the expected need to maintain therapy indefinitely in previously non-irradiated patients. The aim of...
10.
Nascimento G, de Oliveira M, Carvalho V, Lopes M, Sa A, Souza M, et al.
Clin Endocrinol (Oxf)
. 2012 Jun;
78(1):94-101.
PMID: 22702655
Background: A specific acromegaly-related cardiomyopathy has been described in the literature, largely in Caucasians, which is independent of other risk factors, mainly hypertension. Objective: This study assessed the cardiac changes...