Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Camila Ive Ferreira Oliveira"'
Autor:
Angélica Marta Lopes, Patrick Buosi, Bruna de Mattos Farina, Rafael Fernandes-Ferreira, Camila Ive Ferreira Oliveira-Brancati, Denise Poltronieri Martins, Danilo Grünig Humberto da Silva, Nayara Alves Chaves, Lucia Helena Neves Marques, Gerardo Maria de Araújo Filho, Dorotéia Rossi Silva Souza
Publikováno v:
Brain Disorders, Vol 11, Iss , Pp 100099- (2023)
The objective of the present study was to assess the levels of oxidative stress biomarkers (OSB) in patients with pharmacoresistant temporal lobe epilepsy and mesial temporal sclerosis (TLE-MTS) in order to investigate a possible role of oxidative st
Externí odkaz:
https://doaj.org/article/e125cb8ae30c4bf688dc00ba093523de
Autor:
Patrick Buosi, Fábio Aparecido Borghi, Angélica Marta Lopes, Isabela da Silva Facincani, Rafael Fernandes-Ferreira, Camila Ive Ferreira Oliveira-Brancati, Tayanne Silva do Carmo, Dorotéia Rossi Silva Souza, Danilo Grünig Humberto da Silva, Eduardo Alves de Almeida, Gerardo Maria de Araújo Filho
Publikováno v:
Trends in Psychiatry and Psychotherapy, Vol 43, Iss 4, Pp 278-285 (2021)
Abstract Introduction Schizophrenia is a complex psychiatric disorder that affects approximately twenty million people worldwide. Various factors have been associated with the physiopathology of this disease such as oxidative stress, which is an imba
Externí odkaz:
https://doaj.org/article/acac1bc1f61e41448865df1e0d3fa26d
Autor:
Maria Clara Jessica Calastri, Nicolas Luz Toledo Ortega Rodrigues, Gabriela Hatori, Michele Lima Gregório, Camila Ive Ferreira Oliveira Brancati, Eliane Milharcix Zanovelo, José Roberto Lopes Ferraz Filho, Cassiano Merussi Neiva, Antonio Carlos Ponde Rodrigues Junior, Moacir Fernandes de Godoy, Carmen Lucia Penteado Lancelloti, Waldir Antonio Tognola, Dorotéia Rossi Silva Souza
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 76, Iss 6, Pp 393-398
ABSTRACT Background Glioma, the most common primary malignant brain tumor in adults, is highly aggressive and associated with a poor prognosis. The objectives of this study were to evaluate the association of genetic polymorphisms related to angiogen
Externí odkaz:
https://doaj.org/article/e7ecde24fab44aa19bf63b43e08ec429
Autor:
Camila Ive Ferreira Oliveira-Brancati, Valéria Cristina Carvalho Ferrarese, Antonio Richieri Costa, Agnes Cristina Fett-Conte
Publikováno v:
Genetics and Molecular Biology
Abstract Birth defects (BDs) are functional and structural alterations in embryonic or fetal development. With an incidence of approximately 3-5%, BDs are a leading cause of infant mortality and lifelong disability. A population-based prospective cas
Externí odkaz:
https://doaj.org/article/4c784d24c5014129b8be1761dc28675d
Autor:
Beatriz de Jesus Brait, Simone Perpétua da Silva Lima, Franciana Luísa Aguiar, Rafael Fernandes-Ferreira, Camila Ive Ferreira Oliveira-Brancati, Joyce Aparecida Martins Lopes Ferraz, Graciela Domitila Tenani, Marcela Augusta de Souza Pinhel, Leticia Carolina Paraboli Assoni, Augusto Haniu Nakahara, Natalia dos Santos Jábali, Octavio Pennella Fenelon Costa, Maria Eduarda Lopes Baitello, Sidney Pinheiro Júnior, Renato Ferreira Silva, Rita de Cássia Martins Alves Silva, Doroteia Rossi da Silva Souza
Publikováno v:
Ecancermedicalscience. 16
To evaluate the association of genetic polymorphisms of vitamin D transporter protein (A total of 383 individuals were studied, considering the total group (TotalG) of patients with cirrhosis (TotalG
Autor:
Cassiano Merussi Neiva, Gabriela Hattori, Carmen Lucia Penteado Lancellotti, José Roberto Lopes Ferraz Filho, Camila Ive Ferreira Oliveira Brancati, Maria Clara Jessica Calastri, Dorotéia Rossi Silva Souza, Moacir Fernandes de Godoy, Antonio Carlos Ponde Rodrigues Junior, Nicolas Luz Toledo Ortega Rodrigues, Eliane Milharcix Zanovelo, Waldir Antonio Tognola, Michele Lima Gregório
Publikováno v:
Asian Pacific Journal of Cancer Prevention : APJCP
Background: Glioma, most common primary malignant brain tumor in adults, is highly aggressive and associated with a poor prognosis. Evaluate the association of polymorphisms related of to the cell cycle, integrity and DNA repair with gliomas, as well
Autor:
Patrick Buosi, Gerardo Maria de Araújo Filho, Angélica Marta Lopes, Fabio Aparecido Borghi, Eduardo Alves de Almeida, Camila Ive Ferreira Oliveira Brancati, Danilo Antonio da Silva, Tayanne Silva Carmo, Isabela Facincani, Dorotéia Rossi Silva Souza, Rafael Ferreira
Publikováno v:
Trends in Psychiatry and Psychotherapy, Volume: 43, Issue: 4, Pages: 278-285, Published: 17 DEC 2021
Trends in Psychiatry and Psychotherapy v.43 n.4 2021
Trends in Psychiatry and Psychotherapy
Sociedade de Psiquiatria do Rio Grande do Sul
instacron:APRGS
Scopus
Repositório Institucional da UNESP
Universidade Estadual Paulista (UNESP)
instacron:UNESP
Trends in Psychiatry and Psychotherapy, Vol 43, Iss 4, Pp 278-285 (2021)
Trends in Psychiatry and Psychotherapy v.43 n.4 2021
Trends in Psychiatry and Psychotherapy
Sociedade de Psiquiatria do Rio Grande do Sul
instacron:APRGS
Scopus
Repositório Institucional da UNESP
Universidade Estadual Paulista (UNESP)
instacron:UNESP
Trends in Psychiatry and Psychotherapy, Vol 43, Iss 4, Pp 278-285 (2021)
Made available in DSpace on 2022-04-28T19:49:45Z (GMT). No. of bitstreams: 0 Previous issue date: 2021-10-01 INTRODUCTION: Schizophrenia is a complex psychiatric disorder that affects approximately twenty million people worldwide. Various factors hav
Autor:
Valéria Cristina Carvalho Ferrarese, Antonio Richieri da Costa, Camila Ive Ferreira Oliveira-Brancati, Agnes Cristina Fett-Conte
Publikováno v:
Genetics and Molecular Biology
Genetics and Molecular Biology v.43 n.1 2020
Sociedade Brasileira de Genética (SBG)
instacron:SBG
Genetics and Molecular Biology v.43 n.1 2020
Sociedade Brasileira de Genética (SBG)
instacron:SBG
Birth defects (BDs) are functional and structural alterations in embryonic or fetal development. With an incidence of approximately 3-5%, BDs are a leading cause of infant mortality and lifelong disability. A population-based prospective case-control
Autor:
Eduardo Alves de Almeida, Gerardo Maria de Araújo Filho, Ana Eliza Romano Furlan, Dorotéia Rossi Silva Souza, Denise P. Martins, Angélica Marta Lopes, Lucia Helena Neves Marques, Beatriz de Jesus Brait, Camila Ive Ferreira Oliveira
Publikováno v:
Scopus
Repositório Institucional da UNESP
Universidade Estadual Paulista (UNESP)
instacron:UNESP
Repositório Institucional da UNESP
Universidade Estadual Paulista (UNESP)
instacron:UNESP
Made available in DSpace on 2018-12-11T17:17:42Z (GMT). No. of bitstreams: 0 Previous issue date: 2018-03-01 Faculdade de Medicina de São José do Rio Preto Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) Objective: The object
Autor:
Camila Ive Ferreira Oliveira-Brancati, Valéria Cristina Carvalho Ferrarese, Antonio Richieri Costa, Agnes Cristina Fett-Conte
Publikováno v:
Genetics and Molecular Biology, Issue: ahead, Published: 12 AUG 2019
Genetics and Molecular Biology
Genetics and Molecular Biology
Birth defects (BDs) are functional and structural alterations in embryonic or fetal development. With an incidence of approximately 3-5%, BDs are a leading cause of infant mortality and lifelong disability. A population-based prospective case-control
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::a60c77068346d75ee07716d143fc939d
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572019005032101&lng=en&tlng=en
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572019005032101&lng=en&tlng=en