Emilio L Streck
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Explore the profile of Emilio L Streck including associated specialties, affiliations and a list of published articles.
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213
Citations
2891
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Recent Articles
1.
Marcuzzo M, de Andrade Silveira J, Streck E, Vockley J, Leipnitz G
Mol Neurobiol
. 2024 Sep;
PMID: 39251562
Inherited metabolic disorders (IMDs) are genetic disorders often characterized by the accumulation of toxic metabolites in patient tissues and bodily fluids. Although the pathophysiologic effect of these metabolites and their...
2.
Cruz K, Salla D, Oliveira M, Silva L, Vedova L, Mendes T, et al.
Behav Brain Res
. 2023 Jun;
451:114526.
PMID: 37271313
This study aimed to evaluate the behavioral and energy metabolism parameters in female mice subjected to obesity and offspring deprivation (OD) stress. Eighty female Swiss mice, 40 days old, were...
3.
Rodrigues M, Martins J, De Paula G, Venturini L, Silveira G, Streck E, et al.
An Acad Bras Cienc
. 2022 Dec;
94(suppl 4):e20211081.
PMID: 36541976
Cholesterol is a lipid molecule of great biological importance to animal cells. Dysregulation of cholesterol metabolism leads to raised blood total cholesterol levels, a clinical condition called hypercholesterolemia. Evidence has...
4.
Dominguini D, Michels M, Wessler L, Streck E, Barichello T, Dal-Pizzol F
J Neuroinflammation
. 2022 Nov;
19(1):268.
PMID: 36333747
The pathophysiology of sepsis may involve the activation of the NOD-type receptor containing the pyrin-3 domain (NLPR-3), mitochondrial and oxidative damages. One of the primary essential oxidation products is 8-oxoguanine...
5.
Morais F, Lemos I, Matiola R, Freitas M, Alano C, Cabral J, et al.
Metab Brain Dis
. 2022 Apr;
37(5):1585-1596.
PMID: 35394251
Maple Syrup Urine Disease (MSUD) is caused by the deficiency in the activity of the branched-chain α-ketoacid dehydrogenase complex (BCKDC), resulting in the accumulation of the branched-chain amino acids (BCAA)...
6.
de Medeiros B, Wessler L, Duarte M, Lemos I, Candiotto G, Canarim R, et al.
Metab Brain Dis
. 2022 Mar;
37(4):1155-1161.
PMID: 35275349
Maple Syrup Urine Disease (MSUD) is an autosomal recessive inherited disorder caused by a deficiency in the activity of the branched-chain alpha-ketoacid dehydrogenase complex leading to the accumulation of branched-chain...
7.
Scaini G, Andrews T, Lima C, Benevenuto D, Streck E, Quevedo J
Mitochondrion
. 2020 Dec;
57:23-36.
PMID: 33340709
The understanding of the pathophysiology of bipolar disorder (BD) remains modest, despite recent advances in neurobiological research. The mitochondrial dysfunction hypothesis of bipolar disorder has been corroborated by several studies...
8.
Streck E, Bussular F, Wessler L, Duarte M, Rezende V, Rodrigues M, et al.
Metab Brain Dis
. 2020 Oct;
36(2):247-254.
PMID: 33098071
Maple Syrup Urine Disease (MSUD) is an autosomal recessive inherited disorder that affects the activity of the branched-chainα-keto acid dehydrogenase complex (BCDK). This deficiency on BCDK complex results in the...
9.
Farias H, Gabriel J, Cecconi M, Lemos I, de Rezende V, Wessler L, et al.
Metab Brain Dis
. 2020 Oct;
36(1):185-192.
PMID: 33034842
Maple syrup urine disease (MSUD) is characterized by a deficiency in the mitochondrial branched-chain α-keto acid dehydrogenase complex activity and, consequently, accumulation of the branched-chain amino acids and their respective...
10.
Goncalves C, Vasconcelos F, Wessler L, Lemos I, Candiotto G, Lin J, et al.
Metab Brain Dis
. 2020 Sep;
35(8):1407-1416.
PMID: 32876824
Autistic spectrum disorder (ASD) is a group of early-onset neurodevelopmental disorders characterized by impaired social and communication skills. Autism is widely described as a behavioral syndrome with multiple etiologies where...