Zobrazeno 1 - 10 of 33 pro vyhledávání: '"Tatiana Rozov"'
1
Akademický článek
Effects of Pilates mat exercises on muscle strength and on pulmonary function in patients with cystic fibrosis
Autor: Caroline Buarque Franco, Antonio Fernando Ribeiro, André Moreno Morcillo, Mariana Porto Zambon, Marina Buarque Almeida, Tatiana Rozov
Publikováno v: Jornal Brasileiro de Pneumologia, Vol 40, Iss 5, Pp 521-527 (2014)
OBJECTIVE: To analyze the effects of Pilates mat exercises in patients with cystic fibrosis (CF). METHODS: This was a clinical trial involving 19 CF patients recruited from either the CF Outpatient Clinic of the State University at Campinas Hospital
Externí odkaz: https://doaj.org/article/8f811789c7ab4f02a9ade1791cc1d394
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2
Akademický článek
A first-year dornase alfa treatment impact on clinical parameters of patients with cystic fibrosis: the Brazilian cystic fibrosis multicenter study
Autor: Tatiana Rozov, Fernando Antônio A. e Silva, Maria Angélica Santana, Fabíola Villac Adde, Rita Heloisa Mendes
Publikováno v: Revista Paulista de Pediatria, Vol 31, Iss 4, Pp 420-430 (2013)
OBJECTIVE: To describe the clinical impact of the first year treatment with dornase alfa, according to age groups, in a cohort of Brazilian Cystic Fibrosis (CF) patients. METHODS: The data on 152 eligible patients, from 16 CF reference centers, that
Externí odkaz: https://doaj.org/article/2a07e1365fc649d7a40548ee45bf283c
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3
Akademický článek
Validação lingüística dos questionários de qualidade de vida em fibrose cística Linguistic validation of cystic fibrosis quality of life questionnaires
Autor: Tatiana Rozov, Maristela T. Cunha, Oliver Nascimento, Alexandra L. Quittner, José R. Jardim
Publikováno v: Jornal de Pediatria, Vol 82, Iss 2, Pp 151-156 (2006)
OBJETIVO: O propósito deste estudo foi validar em português as quatro versões de questionários de qualidade de vida em fibrose cística, desenvolvidos para pacientes com fibrose cística de 6 a 11 anos, de 12 a 13 e mais de 14 anos, e para os pai
Externí odkaz: https://doaj.org/article/a99aabfb9fcb4812ac772fa9b55c349c
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4
Akademický článek
Displasia broncopulmonar Bronchopulmonary dysplasia
Autor: Luciana F. Velloso Monte, Luiz Vicente F. da Silva Filho, Milton Harumi Miyoshi, Tatiana Rozov
Publikováno v: Jornal de Pediatria, Vol 81, Iss 2, Pp 99-110 (2005)
OBJETIVO: Apresentar uma ampla revisão da literatura sobre displasia broncopulmonar, abordando novas definições, fisiopatologia, prevenção, tratamento, prognóstico e evolução. FONTE DOS DADOS: Foram selecionados os artigos mais relevantes sob
Externí odkaz: https://doaj.org/article/6f4d2d3f348d48d99144832007e6af93
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6
Brazilian guidelines for the diagnosis and treatment of cystic fibrosis
Autor: Rodrigo Abensur Athanazio, Luiz Vicente Ribeiro Ferreira da Silva Filho, Alberto Andrade Vergara, Antônio Fernando Ribeiro, Carlos Antônio Riedi, Elenara da Fonseca Andrade Procianoy, Fabíola Villac Adde, Francisco José Caldeira Reis, José Dirceu Ribeiro, Lídia Alice Torres, Marcelo Bicalho de Fuccio, Matias Epifanio, Mônica de Cássia Firmida, Neiva Damaceno, Norberto Ludwig-Neto, Paulo José Cauduro Maróstica, Samia Zahi Rached, Suzana Fonseca de Oliveira Melo, Leonardo Araújo Pinto, Luciana Freitas Velloso Monte, Laurinda Yoko Shinzato Higa, Tania Wrobel Folescu, Fernando Augusto de Lima Marson, Isabela Sad, Maria de Fátima Correa Pimenta Servidoni, Paulo Kussek, Salmo Raskin, Adriana Della Zuana, Albin Augustin, Anneliese Hoffmann, Beatriz Barbisan, Bruno Hochhegger, Carlos Emilio Levy, Claudine Sarmento da Veiga, Claudio Ricachinevsky, Concetta Esposito, Dante Escuissato, Diego Brandemburgo, Elisabeth Marques, Evanirso de Aquino, Gilberto Bueno Fischer, Joaquim Carlos Rodrigues, Leticia Machado, Lucia Muramato, Lusmaia Damasceno Camargo Costa, Marcio Donadio, Marcos César Santos de Castro, Maria Angela Ribeiro, Maria Angélica Santana, Mariane Canan, Marina Buarque de Almeida, Murilo Britto, Paulo Roth Tarso Dalcin, Regina Terse Trindade Ramos, Sonia Chiba, Valéria de Carvalho Martins, Claudine Lacerda, Eliana Barbosa, Elizabet Vilar Guimarães, Gabriel Hessel, Jocemara Gurmini, Lenycia Neri, Marcelo Coelho Nogueira, Mônica Chang Wayhs, Miriam Isabel Santos Simon, Arlene Gonçalves dos Santos Fernandes, Claudia de Castro de Silva, Cristiano Túlio Maciel Albuquerque, Edna Lúcia Souza, Fernando Antonio de Abreu e Silva, Paulo de Tarso Dalcin, Renata Maria de Noronha, Ricardo Teixeira, Sandra Helena Machado, Spencer Marcantonio Camargo, Tatiana Rozov, Ticiana da Costa Rodrigues
Publikováno v: Jornal Brasileiro de Pneumologia v.43 n.3 2017
Jornal Brasileiro de Pneumologia
Sociedade Brasileira de Pneumologia e Tisiologia (SBPT)
instacron:SBPT
Jornal Brasileiro de Pneumologia, Vol 43, Iss 3, Pp 219-245
Jornal Brasileiro de Pneumologia, Volume: 43, Issue: 3, Pages: 219-245, Published: JUN 2017
Cystic fibrosis (CF) is an autosomal recessive genetic disorder characterized by dysfunction of the CFTR gene. It is a multisystem disease that most often affects White individuals. In recent decades, various advances in the diagnosis and treatment o
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::907f2733abedf1cb23fbf66bc14b0cc1
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1806-37132017000300219
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7
O impacto de primeiro ano de tratamento com dornase alfa nos parâmetros clínicos de pacientes com fibrose cística: estudo multicêntrico brasileiro
Autor: Tatiana Rozov, Fernando Antonio Abreu e Silva, Maria Angélica Santana, Rita Heloisa Mendes, Fabíola Villac Adde
Publikováno v: Revista Paulista de Pediatria, Volume: 31, Issue: 4, Pages: 420-430, Published: DEC 2013
Revista Paulista de Pediatria v.31 n.4 2013
Revista Paulista de Pediatria (Ed. Português. Online)
Sociedade de Pediatria de São Paulo (SPSP)
instacron:SPSP
Revista Paulista de Pediatria, Vol 31, Iss 4, Pp 420-430 (2013)
Revista Paulista de Pediatria
OBJECTIVE: To describe the clinical impact of the first year treatment with dornase alfa, according to age groups, in a cohort of Brazilian Cystic Fibrosis (CF) patients. METHODS: The data on 152 eligible patients, from 16 CF reference centers, that
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::258271d378a94851d2b2699d0f5e6de5
https://doi.org/10.1590/s0103-05822013000400002
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8
Six-minute walk test in healthy children: Is the leg length important?
Autor: José Roberto Jardim, Camila Cruz Rodrigues, Andreia C. Oliveira, Denise S. Rolim, Oliver A. Nascimento, Altay A.L. Souza, Tatiana Rozov
Publikováno v: Pediatric Pulmonology. 48:921-926
Rationale Measures as height, age, and weight influence the six-minute walk test (6MWT). It was shown that children's true leg length (TLL) influence the 6MWT distance but so far it has never been evaluated how much this variable could predict the di
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::562f2f0717b6be1018a71b4d5e0045ad
https://doi.org/10.1002/ppul.22696
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9
Dornase alfa improves the health-related quality of life among Brazilian patients with cystic fibrosis-A one-year prospective study
Autor: Tatiana, Rozov, Viviane Ziebell, de Oliveira, Maria Angélica, Santana, Fabíola Villac, Adde, Rita Heloisa, Mendes, Ilma Aparecida, Paschoal, Francisco J, Caldeira Reis, Laurinda Yoko Shinzato, Higa, Antonio Carlos de Castro, Toledo, Márcia, Pahl, Lívia, Martins
Publikováno v: Pediatric Pulmonology. 45:874-882
Background Health-related quality of life (HRQOL) measurements provide valuable information about the psychological and social impact of treatment on patients with cystic fibrosis (CF). This study evaluated the HRQOL of Brazilian patients with CF and
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::736a86af460d452800748ea016ee5c82
https://doi.org/10.1002/ppul.21267
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10
Incidence of cystic fibrosis in five different states of Brazil as determined by screening of p.F508del, mutation at the CFTR gene in newborns and patients
Autor: Norberto Ludwig, Eurico Camargo Neto, Ranajit Chakraborty, Roberto Giugliani, Fernando Abreu, Eduardo Lewis, Lodercio Culpi, Lairton Valentin, Salmo Raskin, Lilian Pereira-Ferrari, John Atlas Phillip, Edna Maria de Albuquerque Diniz, Francisco J.C. Reis, Tatiana Rozov, Nelson Augusto Rosario-Filho, Paulo José Cauduro Marostica, Joselina Magalhaes Andrade Cardieri
Publikováno v: Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Cystic Fibrosis (CF) is one of the most common single-gene defects in European descent populations with an incidence of about 1 in every 2500 live births and carrier frequency of approximately 1 in 25. The most common mutation at the CF transmembrane
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c4fb68dc8109604802a663fdf022ea96
https://doi.org/10.1016/j.jcf.2007.03.006
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