Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Virgínia Maria Cóser"'
Autor:
Leonardo Leiria de Moura da Silva, Anna Júlia de Borba Andres, Roberta Senger, Ralf Stuermer, Maria Celoni de Mello de Godoy, Eduardo Francisco Mafassioli Correa, Virgínia Maria Cóser
Publikováno v:
Brazilian Journal of Cardiovascular Surgery, Vol 28, Iss 2, Pp 183-189 (2013)
OBJECTIVE: To evaluate the impact of Cell Saver autologous blood transfusion system (CS) on the use of packed red blood cells (pRBC) in coronary artery bypass grafting (CABG) surgery. METHODS: We carried out a retrospective cross-sectional study in 8
Externí odkaz:
https://doaj.org/article/37481ef3b7974a298ad58c0c681b2e35
Autor:
Dayane Bohn Koshiyama, Rafael Fabiano Machado Rosa, Paulo Ricardo Gazzola Zen, Vera Lúcia Berenstein Pereira, Carla Graziadio, Virgínia Maria Cóser, Cláudia Pires Ricachinevsky, Marileila Varella-Garcia, Giorgio Adriano Paskulin
Publikováno v:
Revista da Associação Médica Brasileira, Vol 55, Iss 4, Pp 442-446 (2009)
OBJETIVO: A síndrome de deleção 22q11.2 é considerada hoje uma das doenças genéticas mais frequentes em humanos. Caracteriza-se clinicamente por um espectro fenotípico bastante amplo, com mais de 180 achados já descritos, tanto físicos como
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::1d13a9f882bf4632ffc1021e60e0485b
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0104-42302009000400020
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0104-42302009000400020
Autor:
Bruno Alves, de Aguiar Gonçalves, Gisele M, Vasconcelos, Luiz Claudio Santos, Thuler, Camilla, Andrade, Alessandra, Faro, Maria S, Pombo-de-Oliveira, Mariana, Emerenciano, Beatriz, de Camargo, Luna, Bernstain, Cynthia Curvello, Neves, Jozina Maria de Andrade, Agareno, Lilian Maria Burlacchini, de Carvalho, Flávia Nogueira Serafim, Araújo, Nilma Pimentel, de Brito, Isis Q, Magalhães, José Carlos, Cordoba, Flávia, Pimenta, Andreia, Gadelha, Eloísa, Cartaxo, Rosania Maria, Basegio, Atalla, Mnayarji, Marcelo S, Souza, Alejandro, Arencibia, Renato, Melaragno, Virgínia Maria, Cóser, Thereza Christina, Lafayete, Sergio, Koifman
Publikováno v:
Cancer causescontrol : CCC. 23(11)
The risk of developing childhood leukemia has been associated with gene polymorphisms that decrease the activity of detoxifying metabolic enzymes and enzymes involved in systemic oxidative stress. We investigated the NQO1 and PON1 polymorphisms for a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb8693c59a5b5d3ac49f06dd5a946425
https://pubmed.ncbi.nlm.nih.gov/22976839
https://pubmed.ncbi.nlm.nih.gov/22976839
Autor:
Dayane Bohn, Koshiyama, Rafael Fabiano Machado, Rosa, Paulo Ricardo Gazzola, Zen, Vera Lúcia Berenstein, Pereira, Carla, Graziadio, Virgínia Maria, Cóser, Cláudia Pires, Ricachinevsky, Marileila, Varella-Garcia, Giorgio Adriano, Paskulin
Publikováno v:
Revista da Associacao Medica Brasileira (1992). 55(4)
The 22q11.2 deletion syndrome nowadays is considered one of the most often observed genetic diseases in humans. It is clinically characterized by a rather wide phenotypic spectrum, with more than 180 clinical features physical as well as behavioral,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1860985c2ed71aa2c350974b033c9912
https://pubmed.ncbi.nlm.nih.gov/19750312
https://pubmed.ncbi.nlm.nih.gov/19750312