Julia S Vieira
Overview
Explore the profile of Julia S Vieira including associated specialties, affiliations and a list of published articles.
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Articles
9
Citations
112
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Recent Articles
1.
Ferreira G, Rezin G, Cardoso M, Goncalves C, Borges L, Vieira J, et al.
Acta Neuropsychiatr
. 2016 Mar;
24(2):115-21.
PMID: 26952953
Objectives: Based on the hypothesis that energy impairment may be involved in the pathophysiology of depression, we evaluated the activities of citrate synthase, malate dehydrogenase, succinate dehydrogenase (SDH), mitochondrial respiratory...
2.
Freitas T, Rezin G, Fraga D, Moretti M, Vieira J, Gomes L, et al.
Acta Neuropsychiatr
. 2016 Mar;
23(3):106-11.
PMID: 26952896
Objectives: Bipolar disorder (BD) is a mental illness associated with higher rates of suicide. The present study aims to investigate the brain mitochondrial respiratory chain activity in an animal model...
3.
Lopes-Borges J, Valvassori S, Varela R, Tonin P, Vieira J, Goncalves C, et al.
Pharmacol Biochem Behav
. 2014 Nov;
128:89-95.
PMID: 25433326
Studies have revealed alterations in mitochondrial complexes in the brains of bipolar patients. However, few studies have examined changes in the enzymes of the tricarboxylic acid cycle. Several preclinical studies...
4.
Rezin G, Goncalves C, Daufenbach J, Carvalho-Silva M, Borges L, Vieira J, et al.
Acta Neuropsychiatr
. 2014 Nov;
22(6):292-9.
PMID: 25385216
Unlabelled: Rezin GT, Gonçalves CL, Daufenbach JF, Carvalho-Silva M, Borges LS, Vieira JS, Hermani FV, Comim CM, Quevedo J, Streck EL. Effect of chronic administration of ketamine on the mitochondrial...
5.
De Pra S, Ferreira G, Carvalho-Silva M, Vieira J, Scaini G, Leffa D, et al.
Neurochem Res
. 2013 Dec;
39(1):202-7.
PMID: 24297753
Mutations in the tyrosine aminotransferase gene have been identified to cause tyrosinemia type II which is inherited in an autosomal recessive manner. Studies have demonstrated that an excessive production of...
6.
Macedo L, Carvalho-Silva M, Ferreira G, Vieira J, Olegario N, Goncalves R, et al.
Neurochem Res
. 2013 Oct;
38(12):2625-30.
PMID: 24135880
Tyrosinemia type II, also known as Richner-Hanhart syndrome, is an autosomal recessive inborn error of metabolism caused by a deficiency of hepatic cytosolic tyrosine aminotransferase, and is associated with neurologic...
7.
Steckert A, Comim C, Mina F, Mendonca B, Dominguini D, Ferreira G, et al.
Synapse
. 2013 Jun;
67(11):786-93.
PMID: 23740866
Central nervous system (CNS) dysfunction secondary to sepsis is characterized by long-term cognitive impairment. It was observed that oxidative damage, energetic metabolism impairment, and cytokine level alteration seen in early...
8.
Ferreira G, Carvalho-Silva M, Goncalves C, Vieira J, Scaini G, Ghedim F, et al.
Neurochem Int
. 2012 Oct;
61(8):1370-4.
PMID: 23046746
Tyrosinemia is a rare genetic disease caused by mutations on genes that codify enzymes responsible for tyrosine metabolism. Considering that tyrosinemics patients usually present symptoms associated with central nervous system...
9.
Ferreira G, Scaini G, Carvalho-Silva M, Gomes L, Borges L, Vieira J, et al.
Neurotox Res
. 2012 Aug;
23(4):327-35.
PMID: 22847184
Tyrosinemia is a rare disease caused by a single mutation to the gene that code for the enzyme responsible for tyrosine catabolism. Because the mechanisms underlying the neurological dysfunction in...