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G Leipnitz

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Articles 36
Citations 199
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Recent Articles
1.
Nonose Y, Pieper L, da Silva J, Longoni A, Apel R, Meira-Martins L, et al.
Brain Res . 2020 Sep; 1748:147080. PMID: 32866546
Glutamate (Glu) is the main mammalian brain neurotransmitter. Concerning the glutamatergic neurotransmission, excessive levels of glutamate in the synaptic cleft are extremally harmful. This phenomenon, named as excitotoxicity is involved...
2.
Argenti L, Parmeggiani B, Leipnitz G, Weber A, Pereira G, Bustamante-Filho I
Andrologia . 2018 Feb; PMID: 29388232
Although boar semen productivity is affected by seasonality, its effects are not equal among different regions which raise concerns regarding the profitability of boar stud farms. Therefore, the goals of...
3.
Colin-Gonzalez A, Paz-Loyola A, Serratos I, Seminotti B, Ribeiro C, Leipnitz G, et al.
Neuroscience . 2015 Oct; 310:578-88. PMID: 26431622
Several physiological processes in the CNS are regulated by the endocannabinoid system (ECS). Cannabinoid receptors (CBr) and CBr agonists have been involved in the modulation of the N-methyl-D-aspartate receptor (NMDAr)...
4.
Colin-Gonzalez A, Paz-Loyola A, Serratos I, Seminotti B, Ribeiro C, Leipnitz G, et al.
Neuroscience . 2015 Sep; 308:64-74. PMID: 26343296
The brain of children affected by organic acidemias develop acute neurodegeneration linked to accumulation of endogenous toxic metabolites like glutaric (GA), 3-hydroxyglutaric (3-OHGA), methylmalonic (MMA) and propionic (PA) acids. Excitotoxic...
5.
Borges C, Canani C, Fernandes C, Zanatta A, Seminotti B, Ribeiro C, et al.
Neuroscience . 2015 Jul; 304:122-32. PMID: 26188285
Phytanic acid (Phyt) accumulates in various peroxisomal diseases including Refsum disease (RD) and Zellweger syndrome (ZS). Since the pathogenesis of the neurological symptoms and especially the cerebellar abnormalities in these...
6.
da Rosa M, Seminotti B, Amaral A, Parmeggiani B, de Oliveira F, Leipnitz G, et al.
Neuroscience . 2014 Jul; 277:281-93. PMID: 25043325
High accumulation of D-2-hydroxyglutaric acid (D-2-HG) is the biochemical hallmark of patients affected by the inherited neurometabolic disorder D-2-hydroxyglutaric aciduria (D-2-HGA). Clinically, patients present neurological symptoms and basal ganglia injury...
7.
Viegas C, Zanatta A, Grings M, Hickmann F, Monteiro W, Soares L, et al.
Free Radic Res . 2014 Mar; 48(6):659-69. PMID: 24580146
Hyperammonemia is a common finding in children with methylmalonic acidemia and propionic acidemia, but its contribution to the development of the neurological symptoms in the affected patients is poorly known....
8.
da Rosa M, Seminotti B, Amaral A, Fernandes C, Gasparotto J, Moreira J, et al.
Free Radic Res . 2013 Oct; 47(12):1066-75. PMID: 24127998
3-Hydroxy-3-methylglutaryl-CoA lyase (HL) deficiency is a disorder biochemically characterized by the predominant accumulation of 3-hydroxy-3-methylglutarate (HMG), 3-methylglutarate (MGA), 3-methylglutaconate and 3-hydroxyisovalerate in tissues and biological fluids of the affected patients....
9.
Marcelino T, Longoni A, Kudo K, Stone V, Rech A, de Assis A, et al.
Neuroscience . 2013 May; 246:28-39. PMID: 23639877
Physical exercise during pregnancy has been considered beneficial to mother and child. Recent studies showed that maternal swimming improves memory in the offspring, increases hippocampal neurogenesis and levels of neurotrophic...
10.
Latini A, Scussiato K, Leipnitz G, Gibson K, Wajner M
J Inherit Metab Dis . 2007 Sep; 30(5):800-10. PMID: 17885820
Animal models of inborn errors of metabolism are useful for investigating the pathogenesis associated with the corresponding human disease. Since the mechanisms involved in the pathophysiology of succinate semialdehyde dehydrogenase...