Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Tânia Wrobel Folescu"'
Autor:
Viviane Mauro Correa Meyer, Marilda Mendonça Siqueira, Patricia Fernandes Barreto Machado Costa, Braulia Costa Caetano, Jonathan Christian Oliveira Lopes, Tânia Wrobel Folescu, Fernando do Couto Motta
Publikováno v:
PLoS ONE, Vol 15, Iss 10, p e0240452 (2020)
BackgroundsCystic Fibrosis (CF) is a genetic, multisystemic, progressive illness that causes chronic suppurative lung disease. A major cause of morbimortality in this condition are pulmonary exacerbations. Although classically attributed to bacterial
Externí odkaz:
https://doaj.org/article/9168d1f27e204ce69d89078a57526de6
Autor:
Renata Wrobel Folescu Cohen, Tânia Wrobel Folescu, Pedro Daltro, Marcia Cristina Bastos Boechat, Danielle Ferreira Lima, Elizabeth Andrade Marques, Robson Souza Leão
Publikováno v:
São Paulo Medical Journal, Vol 135, Iss 5, Pp 420-427 (2017)
ABSTRACT CONTEXT AND OBJECTIVE: The prevalence of a variety of potentially pathogenic microorganisms in cystic fibrosis patients, such as methicillin-resistant Staphylococcus aureus (MRSA), has increased over the past decade. Given the increasing pre
Externí odkaz:
https://doaj.org/article/21ac21d33f3243dba5aa5921f94c7ec1
Autor:
Renata Wrobel Folescu Cohen, Tânia Wrobel Folescu, Marcia Cristina Bastos Boechat, Vania Matos Fonseca, Elizabeth Andrade Marques, Robson Souza Leão
Publikováno v:
Clinics, Vol 74 (2019)
OBJECTIVE: High-resolution computed tomography (HRCT) allows the early detection of pathological changes in the lung structure, and reproducible scoring systems can be used to quantify chest computed tomography (CT) findings in patients with cystic f
Externí odkaz:
https://doaj.org/article/a17ceb8a42374ec4b289e5682f8b767e
Autor:
Luiz Vicente Ribeiro Ferreira da Silva Filho, Paulo José Cauduro Maróstica, Rodrigo Abensur Athanazio, Francisco José Caldeira Reis, Neiva Damaceno, Angela Tavares Paes, Adilson Yuuji Hira, David Schlesinger, Fernando Kok, Margarida D. Amaral, Mara Lícia Machado Antunes, Lilian Cristina Ferreira Andries, Virginia Auxiliadora Freitas de Castro, Fabíola Villac Adde, Maria Fernanda Botelho Hernandez Perez, Vera Maria Dantas, Luciana de Freitas Velloso Monte, Adriana Goya, Samia Rached, Lusmaia Damaceno Camargo Costa, Lorenna Junqueira Almeida Prado, Elizabet Vilar Guimarães, Ana Cristina de Carvalho Fernandez Fonseca, Marina Pires Nishi, Carlos Antônio Riedi, Nelson Augusto Rosario Filho, Mariane Gonçalves Martynychen Canan, Maria Inez Machado Fernandes, Albin Eugenio Augustin, Rosângela Villela Garcia, Maria Margarete da Silva Zembrzuski, Kátia Izabel de Oliveira, Anneliese Hoffmann, Cláudio Ricachinevsky, Paulo de Tarso Roth Dalcin, Bruna Ziegler, Daniela de Souza Paiva Borgli, Daniele Menezes Torres Ferrao, Elizabeth Passos Simoes da Silva, Maria Angelica Santana, Maria Amenaide Carvalho Alves de Sousa, Claudia de Castro e Silva, Evalto Monte de Araujo Filho, Tiago Neves Veras, Noberto Ludwig Neto, Luiz Roberto Agea Cutolo, Alberto Andrade Vergara, Suzana Fonseca Oliveira Melo, Maria do Espírito Santo Almeida Moreira, Roberta de Cássia Nunes Cruz Melotti, Fernanda Barbosa dos Santos Malini, Marcelo Bicalho de Fuccio, Bruno Porto Pessoa, Concetta Esposito, Paulo Cesar Kussek, Glaunir Maria Foletto, Leonardo Araujo Pinto, Matias Epifanio, Marcelo Tadday Rodrigues, Marta Cristina Duarte, Daniela Gois Meneses, Valéria de Carvalho Martins, Sônia Elenita Lopes Valente, Arlan de Azevedo Ferreira, Constantino Giovanni Braga Cartaxo, Denise Maria Costa Haidar, Mônica de Cássia Firmida, Marcos César Santos de Castro, Edna Lucia Santos de Souza, Lais Ribeiro Mota, Katharina Vidal de Negreiros Moura, Joaquim Carlos Rodrigues, Cleyde Myriam Aversa Nakaie, Tânia Wrobel Folescu, Izabela Sad, Murilo Carlos Amorim de Britto, Carlos Henrique Medeiros Castelletti, Cláudia Mello Gonçalves, Lucia Muramatu, Gilberto Bueno Fischer, Giesela Fleischer Ferrari, Luciana Oliveira Silvano Tostes, Carmen Silvia Bertuzzo, Fernando Augusto de Lima Marson, Sonia Mayumi Chiba, Marcela Duarte De Sillos
Publikováno v:
Journal of Cystic Fibrosis
Background The Brazilian population has a tri-hybrid composition with a high degree of ethnic admixture. We hypothesized that Brazilian individuals with CF from different Brazilian regions have a specific distribution of CFTR variants. Methods Indivi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf9702131a0c0b3d3a03a6f7fcb7a6de
https://doi.org/10.1016/j.jcf.2020.08.007
https://doi.org/10.1016/j.jcf.2020.08.007
Autor:
Pedro Daltro, Elizabeth Andrade Marques, Danielle Ferreira Lima, Tânia Wrobel Folescu, Robson Souza Leão, Renata Wrobel Folescu Cohen, Marcia Cristina Bastos Boechat
Publikováno v:
Sao Paulo Medical Journal, Volume: 135, Issue: 5, Pages: 420-427, Published: 21 AUG 2017
São Paulo Medical Journal, Vol 135, Iss 5, Pp 420-427 (2017)
Sao Paulo Medical Journal, Issue: ahead, Published: 21 AUG 2017
Sao Paulo Medical Journal v.135 n.5 2017
São Paulo medical journal
Associação Paulista de Medicina
instacron:APM
São Paulo Medical Journal, Vol 135, Iss 5, Pp 420-427 (2017)
Sao Paulo Medical Journal, Issue: ahead, Published: 21 AUG 2017
Sao Paulo Medical Journal v.135 n.5 2017
São Paulo medical journal
Associação Paulista de Medicina
instacron:APM
CONTEXT AND OBJECTIVE: The prevalence of a variety of potentially pathogenic microorganisms in cystic fibrosis patients, such as methicillin-resistant Staphylococcus aureus (MRSA), has increased over the past decade. Given the increasing prevalence o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b70f3f2e9cb9b1a5635f1d00b2b4ad60
https://doi.org/10.1590/1516-3180.2016.0350240317
https://doi.org/10.1590/1516-3180.2016.0350240317
Autor:
Pedro Daltro, Deborah Aragão, Paulo Boechat, Patrícia Costa, Tânia Wrobel Folescu, Renata Wrobel Folescu Cohen
Publikováno v:
Residência Pediátrica. 6:121-126
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::715b7cef89ed3f618d636c3ad09cc086
https://doi.org/10.25060/residpediatr-2016.v6n3-03
https://doi.org/10.25060/residpediatr-2016.v6n3-03
Autor:
A.P.D'a Carvalho-Assef, Orlando Carlos da Conceição-Neto, S.C.S. Ornelas, Elizabeth Andrade Marques, Robson Souza Leão, D.P. Alves, Caio Augusto Martins Aires, Rodolpho Mattos Albano, Tânia Wrobel Folescu
Publikováno v:
New Microbes and New Infections
New Microbes and New Infections, Vol 25, Iss, Pp 49-51 (2018)
New Microbes and New Infections, Vol 25, Iss, Pp 49-51 (2018)
We describe the first detection of a KPC-2- and QnrB-producing Enterobacter cloacae from a patient with cystic fibrosis. The blaKPC-2 and qnrB-1 genes were located in a 79.8-kb plasmid. The presence of blaKPC-2 and qnrB-1 genes was determined by PCR
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21106c3cd37432ccb5a428c233142cfa
https://doi.org/10.1016/j.nmni.2018.06.010
https://doi.org/10.1016/j.nmni.2018.06.010
Autor:
Ana Paula D'Alincourt Carvalho-Assef, Rodolpho Mattos Albano, Rosana Helena Vicente Pereira, Vagner Gonçalves Bernardo, M.C. Plotkowski, Robson Souza Leão, Elenice R. A. Rodrigues, Mônica de Cássia Firmida, Tânia Wrobel Folescu, Elizabeth Andrade Marques
Publikováno v:
Epidemiol Infect
SUMMARYAchromobacter spp. are opportunistic pathogens increasingly recovered from adult patients with cystic fibrosis (CF). We report the characterization of 122 Achromobacter spp. isolates recovered from 39 CF patients by multilocus sequence typing,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf52d3feb16d2463655dbd091d0aa394
https://doi.org/10.1017/s0950268816002624
https://doi.org/10.1017/s0950268816002624
Autor:
Tânia Wrobel Folescu, Viviane Mauro Correa Meyer, Marilda M. Siqueira, Braulia Costa Caetano, Patrícia Costa, Fernando Couto Motta, Jonathan Christian Oliveira Lopes
Publikováno v:
PLoS ONE, Vol 15, Iss 10, p e0240452 (2020)
PLoS ONE
PLoS ONE
BackgroundsCystic Fibrosis (CF) is a genetic, multisystemic, progressive illness that causes chronic suppurative lung disease. A major cause of morbimortality in this condition are pulmonary exacerbations. Although classically attributed to bacterial
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e07564bef66d6d1648baffd99a0b597
https://doi.org/10.1371/journal.pone.0240452
https://doi.org/10.1371/journal.pone.0240452
Autor:
Elizabeth Andrade Marques, Vania Matos Fonseca, Marcia Cristina Bastos Boechat, Tânia Wrobel Folescu, Renata Wrobel Folescu Cohen, Robson Souza Leão
Publikováno v:
Clinics
Clinics, Vol 74 (2019)
Clinics; v. 74 (2019); e1399
Clinics; Vol. 74 (2019); e1399
Universidade de São Paulo (USP)
instacron:USP
Clinics, Volume: 74, Article number: e1399, Published: 21 OCT 2019
Clinics, Vol 74 (2019)
Clinics; v. 74 (2019); e1399
Clinics; Vol. 74 (2019); e1399
Universidade de São Paulo (USP)
instacron:USP
Clinics, Volume: 74, Article number: e1399, Published: 21 OCT 2019
OBJECTIVE: High-resolution computed tomography (HRCT) allows the early detection of pathological changes in the lung structure, and reproducible scoring systems can be used to quantify chest computed tomography (CT) findings in patients with cystic f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34d72545130b66ddc36eaacdaab766d9
https://doi.org/10.6061/clinics/2019/e1399
https://doi.org/10.6061/clinics/2019/e1399