Zobrazeno 1 - 5 of 5 pro vyhledávání: '"Marcos César Santos de Castro"'
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Akademický článek
Comparison of two smoking cessation interventions for inpatients
Autor: Antonio Carlos Ferreira Campos, Angela Santos Ferreira Nani, Vilma Aparecida da Silva Fonseca, Eduardo Nani Silva, Marcos César Santos de Castro, Wolney de Andrade Martins
Publikováno v: Jornal Brasileiro de Pneumologia, Vol 44, Iss 3, Pp 195-201
ABSTRACT Objective: This study aimed to compare the effectiveness of two cognitive behavioral therapy-based smoking cessation interventions initiated during hospitalization and to evaluate the factors related to relapse after discharge. Methods: This
Externí odkaz: https://doaj.org/article/b106a50a50f14fc5b9172649a9660b24
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3
Extensive CFTR sequencing through NGS in Brazilian individuals with cystic fibrosis: unravelling regional discrepancies in the country
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
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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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5
CT quantification of large opacities and emphysema in silicosis: correlations among clinical, functional, and radiological parameters
Autor: Gláucia Zanetti, Marcos César Santos de Castro, Agnaldo José Lopes, Guilhermo Coca Velarde, Bruno Hochhegger, Angela Santos Ferreira, Edson Marchiori, Klaus L. Irion
Publikováno v: Lung. 192(4)
The assessment of the extent of silicosis on chest radiographs is subjective and could be more standardized by using computed tomography (CT) quantification methods. We propose a semiautomatic method of quantifying the anatomical lung damage (LD) (th
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a3f8355773c7118beeb67df1cb3ec376
https://pubmed.ncbi.nlm.nih.gov/24811526
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