Zobrazeno 1 - 9 of 9 pro vyhledávání: '"Simone Scherpenhuijzen"'
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Akademický článek
The CIITA genetic polymorphism rs4774*C in combination with the HLA-DRB1*15:01 allele as a putative susceptibility factor to multiple sclerosis in Brazilian females
Autor: Eduardo R. Paradela, Soniza V. Alves-Leon, André L. S. Figueiredo, Valéria C. S. R. Pereira, Fabíola Malfetano, Letícia F. Mansur, Simone Scherpenhuijzen, Luciana A. Agostinho, Catielly F. Rocha, Fernanda Rueda-Lopes, Emerson Gasparetto, Carmen L. A. Paiva
Publikováno v: Arquivos de Neuro-Psiquiatria, Vol 73, Iss 4, Pp 283-288 (2015)
The objective of this study was to investigate the association between the HLA alleles at the DQA1, DQB1 and DRB1 loci, the CIITA genetic polymorphisms -168A/G and +1614G/C, and susceptibility to multiple sclerosis (MS) in a sample from Rio de Janeir
Externí odkaz: https://doaj.org/article/6cfc53e06d2f4ccfbf6b938089ce425e
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3
No correlation was observed between vitamin D levels and disability of patients with multiple sclerosis between latitudes 18° and 30° South
Autor: Carlos Augusto de Albuquerque Damasceno, Mario Fernandes Pietro Peres, Elisa Teixeira da Rocha, Pamela Emanuele Lacerda, Marcus Goncalves, Adaucto Wanderley da Nobrega-Jr, Tarso Adoni, Suzana C. Nunes Machado, Mônica Koncke Fiuza Parolin, Simone Scherpenhuijzen, Carlos Alberto da Silva de Jesus, Soniza Vieira Alves-Leon, Daniel Lima Varela, Fabio Siquinelli, Rogerio Rizo Morales, Marlise de Castro Ribeiro, Maria Fernanda Mendes, André Palma da Cunha Matta, Letícia Fezer Mansur, Patrick N. Stoney, Audred Cristina Biondo Eboni, Joseph Bruno Bidin Brooks, Henrique Cal, Walter Oleschko Arruda, Caroline Vieira Spessotto, Yara Dadalti Fragoso, Samira Luisa Apostolos-Pereira, Heloisa Helena Ruocco, Paulo Diniz da Gama
Publikováno v: Arquivos de Neuro-Psiquiatria, Vol 75, Iss 1, Pp 3-8
Arquivos de Neuro-Psiquiatria v.75 n.1 2017
Arquivos de neuro-psiquiatria
Academia Brasileira de Neurologia
instacron:ABNEURO
Objective: Vitamin D has taken center stage in research and treatment of multiple sclerosis (MS). The objective of the present study was to assess the serum vitamin D levels of a large population of patients with MS and controls living in a restricte
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::765ca3b38725dd3db6f5d09763f17647
https://doi.org/10.1590/0004-282x20160173
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4
Polymorphisms in the CIITA −168A/G (rs3087456) and CIITA +1614G/C (rs4774) may influence severity in multiple sclerosis patients
Autor: Fabrícia Lima Fontes-Dantas, Eduardo Ribeiro Paradela, Ângelo Maiolino, Valeria Coelho Santa Rita Pereira, João Gabriel Dib Farinhas, Soniza Vieira Alves-Leon, Simone Scherpenhuijzen, André Peres De Oliveira, Ronir Raggio Luiz, Fabíola Rachid Malfetano, Letícia Fêzer Mansur
Publikováno v: Arquivos de Neuro-Psiquiatria v.77 n.3 2019
Arquivos de neuro-psiquiatria
Academia Brasileira de Neurologia
instacron:ABNEURO
Arquivos de Neuro-Psiquiatria, Vol 77, Iss 3, Pp 166-173
Arquivos de Neuro-Psiquiatria, Volume: 77, Issue: 3, Pages: 166-173, Published: MAR 2019
It is currently unknown how genetic factors may influence the clinical course of multiple sclerosis (MS). Objective: We examined the impact of CIITA polymorphisms −168A/G (rs3087456) and +1614G/C (rs4774) on the risk of disability progression, seve
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c5594399539c16974d44c3fbabb78f23
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2019000300166
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5
Serological profile of John Cunningham virus (JCV) in patients with multiple sclerosis
Autor: Daniel Lima Varela, Gutemberg Augusto Cruz dos Santos, Claudio Scorcine, Leticia Fezer, Sidney Gomes, Fabio Siquineli, Audred Cristina Biondo Eboni, Nise Alexandra de Carvalho Sousa, Rogerio Rizo Morales, André Muniz, Yara Dadalti Fragoso, Marlise de Castro Ribeiro, Maria Fernanda Mendes, Luciana Prats Branco, Carlos Augusto de Albuquerque Damasceno, Anderson Kuntz Grzesiuk, Eber Castro Correa, Samira Luisa Apostolos-Pereira, Paulo Diniz da Gama, Tarso Adoni, Henry Koiti Sato, Simone Scherpenhuijzen, Joseph Bruno Bidin Brooks, Monica Fiuza Koncke Parolin, Tereza Cristina Avila Winckler, Marcus Goncalves, Maria Lucia Vellutini Pimentel
Publikováno v: Repositório Institucional da UFJF
Universidade Federal de Juiz de Fora (UFJF)
instacron:UFJF
Arquivos de Neuro-Psiquiatria v.76 n.9 2018
Arquivos de neuro-psiquiatria
Academia Brasileira de Neurologia
instacron:ABNEURO
Arquivos de Neuro-Psiquiatria, Vol 76, Iss 9, Pp 588-591
As opções terapêuticas para esclerose múltipla (EM) modificaram-se ao longo dos últimos anos, trazendo uma nova categoria de drogas com melhor perfil de eficácia. No entanto, estas drogas vieram com um novo perfil de potenciais eventos adversos
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a3d6b58e42d980f515c207d49d455d6
https://repositorio.ufjf.br/jspui/handle/ufjf/9232
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6
Seroconversion of JCV antibodies is strongly associated to natalizumab therapy
Autor: Gutemberg Augusto Santos, Yara Dadalti Fragoso, Leticia Fezer, Sidney Gomes, Nise Alessandra de Carvalho Sousa, Paulo Diniz da Gama, Rogerio Rizo Morales, Simone Scherpenhuijzen, Audred Cristina Biondo Eboni, Suzana Nunes Machado, Joseph Bruno Bidin Brooks, Heloisa Helena Ruocco, Marcus Goncalves, Maria Lucia Vellutini Pimentel
Publikováno v: Journal of Clinical Neuroscience. 61:112-113
Previous infection with John Cunningham virus (JCV) increases the risk of progressive multifocal leukoencephalopathy in patients with multiple sclerosis (MS) undergoing treatment with natalizumab. Patients who test negative for JCV antibodies must be
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd6269912d026861949d2cb4beacf1f9
https://doi.org/10.1016/j.jocn.2018.10.128
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7
The CIITA genetic polymorphism rs4774*C in combination with the HLA-DRB1*15:01 allele as a putative susceptibility factor to multiple sclerosis in Brazilian females
Autor: Valeria Coelho Santa Rita Pereira, Emerson Leandro Gasparetto, Carmen Lucia Antão Paiva, Letícia Fezer Mansur, Fabíola Rachid Malfetano, Luciana de Andrade Agostinho, Simone Scherpenhuijzen, Catielly F Rocha, André Luis dos Santos Figueiredo, Eduardo Ribeiro Paradela, Fernanda C. Rueda-Lopes, Soniza Vieira Alves-Leon
Publikováno v: Arquivos de Neuro-Psiquiatria, Vol 73, Iss 4, Pp 283-288 (2015)
Arquivos de Neuro-Psiquiatria v.73 n.4 2015
Arquivos de neuro-psiquiatria
Academia Brasileira de Neurologia
instacron:ABNEURO
The objective of this study was to investigate the association between the HLA alleles at the DQA1, DQB1 and DRB1 loci, the CIITA genetic polymorphisms -168A/G and +1614G/C, and susceptibility to multiple sclerosis (MS) in a sample from Rio de Janeir
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b46ca2bc2c86fa12903bee8b9815d14
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2015000400283&lng=en&tlng=en
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8
Default-mode network and deep gray-matter analysis in neuromyelitis optica patients
Autor: Fernanda M C Pessôa, Soniza Vieira Alves-Leon, Simone Scherpenhuijzen, Fabíola Rachid Malfetano, Emerson Leandro Gasparetto, Fernanda Cristina Rueda-Lopes, Gustavo Tukamoto
Publikováno v: Journal of neuroradiology = Journal de neuroradiologie. 45(4)
The aim of our study was to detect functional changes in default-mode network of neuromyelitis optica (NMO) patients using resting-state functional magnetic resonance images and the evaluation of subcortical gray-matter structures volumes.NMO patient
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ea3d7b3b8ea95c480c9c05a87a368ec
https://pubmed.ncbi.nlm.nih.gov/29470996
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