Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Natália Gindri Fiorenza"'
Autor:
Michele Rechia Fighera, Luiz Fernando Freire Royes, Ana Flávia Furian, Mauro Schneider Oliveira, Natália Gindri Fiorenza, Roberto Frussa-Filho, João Carlos Petry, Rafael Correa Coelho, Carlos Fernando Mello
Publikováno v:
Neurobiology of Disease, Vol 22, Iss 3, Pp 611-623 (2006)
Monosialoganglioside (GM1) is a glycosphingolipid that protects against some neurological conditions, such as seizures and ischemia. Glutaric acidemia type I (GA-I) is an inherited disease characterized by striatal degeneration, seizures, and accumul
Externí odkaz:
https://doaj.org/article/2046a9c0a62443df8fac072c238c39ba
Publikováno v:
Neuroscience and Medicine. :232-238
Memory traces become labile at the time of retrieval, and this initiates two protein synthesis-dependent processes in the brain: extinction, which inhibits their further retrieval, and reconsolidation, which may enhance retrieval or change the memory
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ba534ff21662ac1eef54cbd634ff8249
https://doi.org/10.4236/nm.2011.23032
https://doi.org/10.4236/nm.2011.23032
Autor:
Denise Bohrer, Ana Flávia Furian, Luiz Fernando Freire Royes, Esper Abraão Cavalheiro, Mauro Schneider Oliveira, Juliano Ferreira, Marcelo Castelli, Pablo Machado, Natália Gindri Fiorenza, Marlei Veiga, Michele Rechia Fighera, Carlos Fernando Mello
Publikováno v:
Epilepsy Research. 79:14-21
Cyclooxygenases (COXs) are rate-limiting enzymes in the metabolic pathways in which arachidonic acid is converted to prostaglandins. COX-2 is the isoform induced at injury/inflammation sites and expressed constitutively in a few tissues, such as the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2568f7babecb4e2defe1cd2665c3665
https://doi.org/10.1016/j.eplepsyres.2007.12.008
https://doi.org/10.1016/j.eplepsyres.2007.12.008
Autor:
João Carlos Petry, Mauro Schneider Oliveira, Roberto Frussa-Filho, Rafael Correa Coelho, Michele Rechia Fighera, Carlos Fernando Mello, Ana Flávia Furian, Luiz Fernando Freire Royes, Natália Gindri Fiorenza
Publikováno v:
Neurobiology of Disease, Vol 22, Iss 3, Pp 611-623 (2006)
Monosialoganglioside (GM1) is a glycosphingolipid that protects against some neurological conditions, such as seizures and ischemia. Glutaric acidemia type I (GA-I) is an inherited disease characterized by striatal degeneration, seizures, and accumul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4017f00937fd83f96f2fa5c173f6549e
http://www.sciencedirect.com/science/article/pii/S0969996106000040
http://www.sciencedirect.com/science/article/pii/S0969996106000040
Autor:
Luiz Fernando Freire Royes, Margareth Rose Priel, João B. Calixto, Natália Gindri Fiorenza, André César da Silva, Juliano Ferreira, Ana Flávia Furian, Esper A. Cavalheiro, Mauro Schneider Oliveira, Michele Rechia Fighera, Carlos Fernando Mello, Érika Sayuri Ueda
Publikováno v:
Neurochemistry international. 53(1-2)
The creatine (Cr) and phosphocreatine (PCr) system is essential for the buffering and transport of high-energy phosphates. Although achievements made over the last years have highlighted the important role of creatine in several neurological diseases
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82c84b6b63824249aa062eab8ddba7e1
https://pubmed.ncbi.nlm.nih.gov/18541342
https://pubmed.ncbi.nlm.nih.gov/18541342
Autor:
Mauro Schneider Oliveira, Natália Gindri Fiorenza, Juliano Ferreira, Michele Rechia Fighera, Danieli Valnes Magni, Carlos Fernando Mello, Luiz Fernando Freire Royes, Ana Flávia Furian
Publikováno v:
Brain research. 1185
Glutaric acidemia type I (GA-I) is an inherited metabolic disease characterized by striatal degeneration, seizures, and accumulation of glutaric acid (GA). Considering that GA impairs energy metabolism and induces reactive species generation, we inve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d23dd25b659df020784c2a0f9aa02434
https://pubmed.ncbi.nlm.nih.gov/17950259
https://pubmed.ncbi.nlm.nih.gov/17950259
Autor:
Natália Gindri Fiorenza, Maribel Antonello Rubin, Mauro Schneider Oliveira, Juliano Ferreira, Ana Flávia Furian, Michele Rechia Fighera, Carlos Fernando Mello, Luiz Fernando Freire Royes
Publikováno v:
Behavioural brain research. 187(1)
Achievements made over the last years have highlighted the important role of creatine in health and disease. However, studies of its effect on cognition function have been limited. In the present study, we investigated the effect of creatine on early
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d9c7616faa58975278c460ff33ef182
https://pubmed.ncbi.nlm.nih.gov/17950476
https://pubmed.ncbi.nlm.nih.gov/17950476
Autor:
Luiz Fernando Freire Royes, Natália Gindri Fiorenza, Michele Rechia Fighera, Rudi Weiblen, Ana Flávia Furian, Carlos Fernando Mello, Jociane de Carvalho Myskiw, Maribel Antonello Rubin, Mauro Schneider Oliveira, Roberto Frussa-Filho
Publikováno v:
Free radical biologymedicine. 43(6)
Monosialoganglioside (GM1) is a glycosphingolipid present in most cell membranes that displays antioxidant and neuroprotective properties. GM1 increases catalase activity in cerebral cortices in vivo, but the mechanisms underlying this effect of GM1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd7a79c47f35c1686206ba47d0e57860
https://pubmed.ncbi.nlm.nih.gov/17697937
https://pubmed.ncbi.nlm.nih.gov/17697937
Autor:
Natália Gindri Fiorenza, Michele Rechia Fighera, Carlos Fernando Mello, João Carlos Petry, Rafael Correa Coelho, Mauro Schneider Oliveira, Luiz Fernando Freire Royes, Ana Flávia Furian
Publikováno v:
Epilepsy research. 73(3)
Summary Methylmalonic acidemias consist of a group of inherited metabolic disorders caused by deficiency of methylmalonyl-CoA mutase activity and biochemically characterized by methylmalonate (MMA) accumulation, impairment mitochondrial oxidative met
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1e94693c4943358dd7bf6701c50e37b
https://pubmed.ncbi.nlm.nih.gov/17137751
https://pubmed.ncbi.nlm.nih.gov/17137751
Autor:
João Carlos Petry, Natália Gindri Fiorenza, Luiz Fernando Freire Royes, Ana Flávia Furian, Ana Paula de Oliveira Ferreira, Mauro Schneider Oliveira, Michele Rechia Fighera, Rafael Correa Coelho, Carlos Fernando Mello, Jociane de Carvalho Myskiw
Publikováno v:
Neurochemistry international. 50(1)
Methylene blue (MB) is a thiazine dye with cationic and lipophilic properties that acts as an electron transfer mediator in the mitochondria. Due to this metabolic improving activity and free radicals scavenging effects, MB has been used in the treat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb267cd9e24a67bdafcd2938bb8df569
https://pubmed.ncbi.nlm.nih.gov/16963161
https://pubmed.ncbi.nlm.nih.gov/16963161