Zobrazeno 1 - 8 of 8 pro vyhledávání: '"Rafael Breglio Marchesini"'
1
Akademický článek
Linkage study of voltage-gated potassium channels in familial mesial temporal lobe epilepsy Análise de ligação dos canais de potássio voltagem-dependente na epilepsia de lobo temporal mesial familiar
Autor: Cláudia Vianna Maurer-Morelli, Rafael Breglio Marchesini, Rodrigo Secolin, Neide Ferreira Santos, Eliane Kobayashi, Fernando Cendes, Iscia Lopes-Cendes
Publikováno v: Arquivos de Neuro-Psiquiatria, Vol 65, Iss 1, Pp 20-23 (2007)
Voltage-gated potassium channels (VGKCs) play a critical role in the regulation of neuronal excitability and have been implicated in some types of epilepsies. Recently, autoimmune limbic encephalitis (LE) was associated with antibodies against VGKC.
Externí odkaz: https://doaj.org/article/3dcc5c8d1bc34159bbcae8f2f8ec50b0
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2
Akademický článek
A locus identified on chromosome18p11.31 is associated with hippocampal abnormalities in a family with mesial temporal lobe epilepsy
Autor: Claudia Vianna Maurer-Morelli, Rodrigo eSecolin, Marcia Elisabete eMorita, Romenia Ramos Domingues, Rafael Breglio Marchesini, Neide Ferreira Santos, Eliane eKobayashi, Fernando eCendes, Iscia eLopes-Cendes
Publikováno v: Frontiers in Neurology, Vol 3 (2012)
We aimed to identify the region harboring a putative candidate gene associated with hippocampal abnormalities (HAb) in a family with mesial temporal lobe epilepsy (MTLE). Genome-wide scan was performed in one large kindred with MTLE using a total of
Externí odkaz: https://doaj.org/article/0f5f8aa078f14142b2c4490fb5d72762
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3
Expression Profile and Distribution of Efhc1 Gene Transcript During Rodent Brain Development
Autor: Vinicius D'Ávila Bitencourt Pascoal, Jackson C. Bittencourt, Fábio F. Conte, Iscia Lopes-Cendes, Lourenço Sbragia, Rafael Breglio Marchesini, Rovilson Gilioli, Amanda Ribeiro de Oliveira, Patrícia A. O. Ribeiro, Joelcimar M. da Silva
Publikováno v: Journal of Molecular Neuroscience. 39:69-77
One of the putative causative genes for juvenile myoclonic epilepsy (JME) is EFHC1. We report here the expression profile and distribution of Efhc1 messenger RNA (mRNA) during mouse and rat brain development. Real-time polymerase chain reaction revea
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea83398a641e2a06dd9fb136b51c4d4f
https://doi.org/10.1007/s12031-009-9179-6
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4
Linkage study of voltage-gated potassium channels in familial mesial temporal lobe epilepsy
Autor: Rodrigo Secolin, Iscia Lopes-Cendes, Cláudia Vianna Maurer-Morelli, Fernando Cendes, Neide Ferreira Santos, Rafael Breglio Marchesini, Eliane Kobayashi
Publikováno v: Arquivos de Neuro-Psiquiatria, Volume: 65, Issue: 1, Pages: 20-23, Published: MAR 2007
Arquivos de Neuro-Psiquiatria v.65 n.1 2007
Arquivos de neuro-psiquiatria
Academia Brasileira de Neurologia
instacron:ABNEURO
Voltage-gated potassium channels (VGKCs) play a critical role in the regulation of neuronal excitability and have been implicated in some types of epilepsies. Recently, autoimmune limbic encephalitis (LE) was associated with antibodies against VGKC.
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0fc244551c157a983fafff61e42a41c
https://doi.org/10.1590/s0004-282x2007000100006
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5
A locus identified on chromosome18p11.31 is associated with hippocampal abnormalities in a family with mesial temporal lobe epilepsy
Autor: Fernando Cendes, Rodrigo Secolin, Neide Ferreira Santos, Rafael Breglio Marchesini, Cláudia Vianna Maurer-Morelli, Eliane Kobayashi, Iscia Lopes-Cendes, Romenia Ramos Domingues, Marcia Elisabete Morita
Publikováno v: Frontiers in Neurology, Vol 3 (2012)
Frontiers in Neurology
We aimed to identify the region harboring a putative candidate gene associated with hippocampal abnormalities (HAb) in a family with mesial temporal lobe epilepsy (MTLE). Genome-wide scan was performed in one large kindred with MTLE using a total of
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::551544866d335322c7bf54d33defdc22
http://journal.frontiersin.org/Journal/10.3389/fneur.2012.00124/full
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6
The il1β have a protective action in the acute phase of the pilocarpine-induced epilepsy model
Autor: Licio A. Velloso, Fábio F. Conte, Luciene Covolan, Jackeline Moraes Malheiros, Anabela hb Matos, Rovilson Gilioli, Tiago Campos Pereira, Rafael Breglio Marchesini, Roberson Saraiva Polli, Vinicius D'Ávila Bitencourt Pascoal, Esper A. Cavalheiro, Fernando Cendes, Hilde H Buzzá, Iscia Lopes-Cendes, Alberto Tannus
Publikováno v: Journal of Epilepsy and Clinical Neurophysiology, Volume: 16, Issue: 3, Pages: 97-99, Published: SEP 2010
Journal of Epilepsy and Clinical Neurophysiology v.16 n.3 2010
Journal of epilepsy and clinical neurophysiology
Liga Brasileira de Epilepsia (LBE)
instacron:LBE
Repositório Institucional da UNIFESP
Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
INTRODUÇÃO: Existem contradições na literatura quanto aos efeitos dos genes il1β e il1rn nas epilepsias. Nosso objetivo foi avaliar os efeitos do silenciamento desses dois genes na fase aguda do modelo de epilepsia induzido pela pilocarpina. MÉ
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2bd468e0d1662e1b5dc432e312b5d28b
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1676-26492010000300003&lng=en&tlng=en
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7
Schistosoma mansoni: evaluation of an RNAi-based treatment targeting HGPRTase gene
Autor: Vinicius D'Ávila Bitencourt Pascoal, Ivan de Godoy Maia, Rafael Breglio Marchesini, Iscia Lopes-Cendes, Eliana Maria Zanotti-Magalhães, Luis Alexandre Gonçalves Magalhães, Tiago Campos Pereira
Publikováno v: Experimental parasitology. 118(4)
Hypoxanthine-guanine phosphoribosyltransferase (HGPRTase) is an essential gene of the parasite Schistosoma mansoni and it is well conserved in its hosts (mouse and human) at the protein but not at the RNA level. This feature prompted us to assess RNA
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3673fd6bb98ce27e35f7820a59e85b30
https://pubmed.ncbi.nlm.nih.gov/18237732
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8
THE SCN2A gene is not a likely candidate for familial mesial temporal lobe epilepsy
Autor: Fernando Cendes, Neide Ferreira Santos, Cláudia Vianna Maurer-Morelli, Rodrigo Secolin, Iscia Lopes-Cendes, Rafael Breglio Marchesini, Eliane Kobayashi
Publikováno v: Epilepsy research. 71(2-3)
A transgenic mouse model carrying a mutation in the Scn2a gene showed chronic focal seizures associated with extensive cell loss and gliosis in the hippocampus, a similar phenotype found in familial mesial temporal lobe epilepsy (FMTLE). Our objectiv
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::423678912d764fb99441552267c4a9dd
https://pubmed.ncbi.nlm.nih.gov/16914293
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