Flavia Imbroisi Valle Errera
Overview
Explore the profile of Flavia Imbroisi Valle Errera including associated specialties, affiliations and a list of published articles.
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Articles
12
Citations
105
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Recent Articles
1.
Meira D, Zetum A, Casotti M, Campos da Silva D, de Araujo B, Vicente C, et al.
Heliyon
. 2025 Jan;
10(14):e34393.
PMID: 39816364
Since December 2019, a new form of Severe Acute Respiratory Syndrome (SARS) has emerged worldwide, caused by SARS coronavirus 2 (SARS-CoV-2). This disease was called COVID-19 and was declared a...
2.
Garcia F, de Sousa V, Silva-Dos-Santos P, Fernandes I, Sarquis Serpa F, Paula F, et al.
Clin Rev Allergy Immunol
. 2025 Jan;
68(1):4.
PMID: 39755867
Asthma is a complex disease with varied clinical manifestations resulting from the interaction between environmental and genetic factors. While chronic airway inflammation and hyperresponsiveness are central features, the etiology of...
3.
Casotti M, Meira D, Zetum A, Campanharo C, Campos da Silva D, Giacinti G, et al.
Front Oncol
. 2024 Sep;
14:1419599.
PMID: 39224803
Cancer therapy is facing increasingly significant challenges, marked by a wide range of techniques and research efforts centered around somatic mutations, precision oncology, and the vast amount of big data....
4.
Barcelos E, Naslavsky M, Fernandes I, Scliar M, Yamamoto G, Wang J, et al.
Sci Rep
. 2024 Jul;
14(1):17096.
PMID: 39048597
Excessive weight (overweight and obesity) is a common disorder involving genetic and environmental factors, associated with cardiovascular diseases, type-2 diabetes, and others. NOTCH1 is critical for the maintenance of stem...
5.
Barcelos E, Rompietti C, Adamo F, Dorillo E, De Falco F, Del Papa B, et al.
Front Oncol
. 2023 Oct;
13:1218989.
PMID: 37817771
Introduction: Constitutive activation of -wild-type (NT1-WT) signaling is associated with poor outcomes in chronic lymphocytic leukemia (CLL), and mutation (c.7541_7542delCT), which potentiates NOTCH1 signaling, worsens the prognosis. However, the specific...
6.
Alves L, Meira D, Merigueti L, Casotti M, do Prado Ventorim D, Ferreira Figueiredo Almeida J, et al.
Genes (Basel)
. 2023 Jul;
14(7).
PMID: 37510269
Breast cancer is the second most frequent cancer in the world. It is a heterogeneous disease and the leading cause of cancer mortality in women. Advances in molecular technologies allowed...
7.
Bride L, Naslavsky M, Yamamoto G, Scliar M, Pimassoni L, Sossai Aguiar P, et al.
PeerJ
. 2021 May;
9:e11349.
PMID: 33996288
Background: Type 2 diabetes mellitus (T2DM) and obesity are complex pandemic diseases in the 21st century. Worldwide, the T allele rs7903146 in the gene is recognized as a strong GWAS...
8.
Dos Santos L, Pimassoni L, Sena G, Camporez D, Belcavello L, Trancozo M, et al.
J Mol Neurosci
. 2017 May;
62(2):215-221.
PMID: 28477215
Late-onset Alzheimer's disease (LOAD) is a multifactorial neurodegenerative disorder that corresponds to most Alzheimer's disease (AD) cases. Inflammation is frequently related to AD, whereas microglial cells are the major phagocytes...
9.
Dos Santos L, Belcavello L, Camporez D, de Magalhaes C, Zandonade E, Morelato R, et al.
Neurosci Lett
. 2016 Jan;
614:65-9.
PMID: 26733302
Genome-wide association study (GWAS) has identified several novel genes associated with the risk of Alzheimer's disease (AD), which is a progressive neurodegenerative disease in elders. However, most of the novel...
10.
Faria A, Rabbi-Bortolini E, Reboucas M, de S Thiago Pereira A, Frasson M, Atique R, et al.
Am J Med Genet A
. 2015 Nov;
170A(2):403-409.
PMID: 26566760
Approximately a hundred patients with terminal 10q deletions have been described. They present with a wide range of clinical features always accompanied by delayed development, intellectual disability and craniofacial dysmorphisms....