Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Jaderson C Da Costa"'
Autor:
Fernanda S Rodrigues, Mauren A Souza, Danieli V Magni, Ana Paula O Ferreira, Bibiana C Mota, Andreia M Cardoso, Mariana Paim, Léder L Xavier, Juliano Ferreira, Maria Rosa C Schetinger, Jaderson C Da Costa, Luiz Fernando F Royes, Michele R Fighera
Publikováno v:
PLoS ONE, Vol 8, Iss 10, p e78332 (2013)
BACKGROUND AND AIMS:Glutaric aciduria type I (GA-I) is characterized by accumulation of glutaric acid (GA) and neurological symptoms, such as cognitive impairment. Although this disease is related to oxidative stress and inflammation, it is not known
Externí odkaz:
https://doaj.org/article/05538c45f80248b6a54814e817f9a871
Autor:
Daniel R. Marinowic, Gabriele G. Zanirati, Fernando A. C. Xavier, Fábio Jean Varella, Sofia Prates da Cunha Azevedo, Isadora Machado Ghilardi, Normando G. Pereira-Neto, Marco Antônio Eduardo Koff, Eliseu Paglioli, André Palmini, José Garcia Abreu, Denise C. Machado, Jaderson C. da Costa
Publikováno v:
BMC Neurology, Vol 23, Iss 1, Pp 1-11 (2023)
Abstract Background Focal cortical dysplasia (FCD) is a malformation of cortical development that causes medical refractory seizures, and one of the main treatments may be surgical resection of the affected area of the brain. People affected by FCD m
Externí odkaz:
https://doaj.org/article/495e29782c79466592553e4ae70bc3ec
Autor:
Matheus V.C. Grahl, Allan M. Alcará, Ana Paula A. Perin, Carlo F. Moro, Éderson S.M. Pinto, Bruno C. Feltes, Isadora M. Ghilardi, Felipe V.F. Rodrigues, Marcio Dorn, Jaderson C. da Costa, Osmar Norberto de Souza, Rodrigo Ligabue-Braun
Publikováno v:
Informatics in Medicine Unlocked, Vol 23, Iss , Pp 100539- (2021)
In 2020 SARS-CoV-2 reached pandemic status, reaching Brazil in mid-February. As of now, no specific drugs for treating the disease are available. In this work, the possibility of interaction between SARS-CoV-2 viral proteins (open and closed spike pr
Externí odkaz:
https://doaj.org/article/fda32d86fac24b0e9fea4dbe2d44959d
Autor:
Daniel Marinowic, Gabriele G. Zanirati, Fernanda Majolo, Fernando A. C. Xavier, Felipe V. F. Rodrigues, Eliseu P. Neto, André L. F. Palmini, José G. de Abreu, Denise C. Machado, Jaderson C. da Costa
Background Focal cortical dysplasia (FCD) is a malformation of the cortical development that cause medical refractory seizures and the only treatment may be surgical resection of the affected area of the brain. People affected by FCD may present seiz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aa134802e3f45d93010d2f70fd6f9662
https://doi.org/10.21203/rs.3.rs-1128423/v1
https://doi.org/10.21203/rs.3.rs-1128423/v1
Autor:
Mario S. Palma, Jackson C. Bittencourt, Andrea A. Tavares, Carol F. Elias, Jaderson C. Da Costa, Lilian M. M. Cesar-Tognoli, Simone D. Salamoni
Publikováno v:
Toxins, Vol 3, Iss 2, Pp 142-162 (2011)
The 6-hydroxytrypargine (6-HT) is an alkaloidal toxin of the group of tetrahydro-b-carbolines (THbC) isolated from the venom of the colonial spider Parawixia bistriata. These alkaloids are reversible inhibitors of the monoamine-oxidase enzyme (MAO),
Externí odkaz:
https://doaj.org/article/a00654b2dd354fcbad0cbc758bd2fe18
Autor:
Andreia Rocha, Bruna Bellaver, Luiza Machado, Carolina Soares, Pâmela C. L. Ferreira, Samuel Greggio Gianina T. Venturin, Jaderson C. da Costa, Diogo O. Souza, Eduardo R. Zimmer
Publikováno v:
Dementia & Neuropsychologia.
Background: Recent evidences have pointed to astrocytes as important players in the Alzheimer’s Disease (AD) pathogenesis. Objective: With this in mind, we aim to longitudinally investigate astrocyte changes in a new important AD transgenic model,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4fbf60477e4256db7490a3bde45047cc
https://doi.org/10.5327/1980-5764.rpda023
https://doi.org/10.5327/1980-5764.rpda023
Autor:
Alessandra M. Pereira, Brunno M. Campos, Ana C. Coan, Luiz F. Pegoraro, Thiago J. R. de Rezende, Ignacio Obeso, Paulo Dalgalarrondo, Jaderson C. da Costa, Jean-Claude Dreher, Fernando Cendes
Publikováno v:
Frontiers in Neurology
Frontiers in Neurology, Vol 9 (2018)
Frontiers in Neurology, Vol 9 (2018)
Autism spectrum disorders (ASD) represent a complex group of neurodevelopmental conditions characterized by deficits in communication and social behaviors. We examined the functional connectivity (FC) of the default mode network (DMN) and its relatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1afc32deb49132f49cebc8f35cdb3c1a
http://europepmc.org/articles/PMC6048242
http://europepmc.org/articles/PMC6048242
Autor:
Yasmine, Nonose, Pedro E, Gewehr, Roberto F, Almeida, Jussemara S, da Silva, Bruna, Bellaver, Leo A M, Martins, Eduardo R, Zimmer, Samuel, Greggio, Gianina T, Venturin, Jaderson C, Da Costa, André, Quincozes-Santos, Luc, Pellerin, Diogo O, de Souza, Adriano M, de Assis
Publikováno v:
Molecular neurobiology. 55(3)
This study was performed to evaluate the bilateral effects of focal permanent ischemia (FPI) on glial metabolism in the cerebral cortex. Two and 9 days after FPI induction, we analyze [
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::bc3e9b178dd2ac1b631989ecfddededa
https://pubmed.ncbi.nlm.nih.gov/28271402
https://pubmed.ncbi.nlm.nih.gov/28271402
Autor:
Iscia Lopes-Cendesi, Hélio G.A. Teive, Maria E Calcagnotto, Jaderson C. da Costa, Francisco Cardoso, Erika Viana, Jaime A. Maciel, João Radvany, Walter O. Arruda, Paulo C. Trevisol-Bittencourt, Pedro Rosa Neto, Isabel Silveira, Carlos E. Steiner, Walter Pinto-Júnior, André S. Santos, Ylmar Correa Neto, Lineu C. Werneck, Abelardo Q.C. Araújo, Gerson Carakushansky, Luiz R. Mello, Laura B. Jardim, Guy A. Rouleau
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 55, Iss 3B, Pp 519-529 (1997)
Spinocerebellar ataxia type 1 (SCA1), spinocerebellar ataxia type 2 (SCA2) and Machado-Joseph disease or spinocerebellar ataxia type 3 (MJD/SCA3) are three distinctive forms of autosomal dominant spinocerebellar ataxia (SCA) caused by expansions of a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::e4f440e3040377749cafe1819bc46a24
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X1997000400001
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X1997000400001
Publikováno v:
Movement disorders : official journal of the Movement Disorder Society. 21(7)
Spinocerebellar ataxia (SCA) types 2 and 3 are autosomal-dominant neurodegenerative disorders caused by mutations in two different genes. We identified mutations for SCA2 and SCA3 segregating simultaneously in a single Brazilian family. The index pat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ad2075404e18580c2b84b3ed2c8f585c
https://pubmed.ncbi.nlm.nih.gov/16628604
https://pubmed.ncbi.nlm.nih.gov/16628604