Zobrazeno 1 - 10
of 71
pro vyhledávání: '"Antônio Fernando Ribeiro"'
Autor:
Emília da Silva Gonçalves, José Dirceu Ribeiro, Fernando Augusto Lima Marson, Ciro Garcia Montes, Antônio Fernando Ribeiro, Jochen Georg Mainz, Adyléia Aparecida Dalbo Contrera Toro, Juliana Helena Zamariola, Daniela Souza Paiva Borgli, Elizete Aparecida Lomazi, Maria de Fátima Corrêa Pimenta Servidoni
Publikováno v:
Jornal de Pediatria, Vol 99, Iss 3, Pp 269-277 (2023)
Objective: To assess the prevalence of GERD exclusively by means of multichannel intraluminal impedanciometry associated with pH monitoring (MIIpH) and compare it with respiratory symptoms in children with CF. To compare MIIpH with pHmetry alone to p
Externí odkaz:
https://doaj.org/article/16a1f69a8a2f42828bd2d5262daf9871
Publikováno v:
Jornal Brasileiro de Pneumologia, Vol 49, Iss 1 (2023)
ABSTRACT Objective: To analyze the characteristics of cystic fibrosis (CF) care centers (CFCCs) in Brazil. Methods: A questionnaire was sent to the coordinators of all 51 registered CFCCs between May and September of 2021. Results: The response rate
Externí odkaz:
https://doaj.org/article/d96b38ec61834b9e9cc3a6a46ed92a3b
Autor:
Aline Cristina Gonçalves, Fernando Augusto Lima Marson, Regina Maria Holanda Mendonça, Carmen Sílvia Bertuzzo, Ilma Aparecida Paschoal, José Dirceu Ribeiro, Antônio Fernando Ribeiro, Carlos Emílio Levy
Publikováno v:
Jornal de Pediatria (Versão em Português), Vol 95, Iss 4, Pp 443-450 (2019)
Objective: Cystic fibrosis diagnosis is dependent on the chloride ion concentration in the sweat test (≥ 60 mEq/mL – recognized as the gold standard indicator for cystic fibrosis diagnosis). Moreover, the salivary glands express the CFTR protein
Externí odkaz:
https://doaj.org/article/2f00a222ffc54c69bd8070a8f392db30
Autor:
Carla Cristina Souza Gomez, Fernando Augusto Lima Marson, Maria Fátima Servidoni, Antônio Fernando Ribeiro, Maria Ângela Gonçalves Oliveira Ribeiro, Veruska Acioli Lopes Gama, Eduardo Tavares Costa, José Dirceu Ribeiro, Francisco Ubaldo Vieira Junior
Publikováno v:
BMC Pulmonary Medicine, Vol 18, Iss 1, Pp 1-16 (2018)
Abstract Background The sweat test (ST) is the gold standard for the diagnosis of cystic fibrosis (CF). However, little is known about sweat induction using different types of currents and waves. In this context, our objective was to develop a device
Externí odkaz:
https://doaj.org/article/3315d37f07cf4809855d7c6697b46006
Autor:
Aline Cristina Gonçalves, Fernando Augusto Lima Marson, Regina Maria Holanda Mendonça, José Dirceu Ribeiro, Antônio Fernando Ribeiro, Carlos Emílio Levy
Publikováno v:
Brazilian Journal of Oral Sciences, Vol 17 (2018)
The oral health in patients with cystic fibrosis (CF) is not well studied. Aim: In this context, we describe the frequency of dental problems and performed the description of plaque index and gingival index in patients with CF. Methods: We performed
Externí odkaz:
https://doaj.org/article/5c0db07c587e4e668bb71bad55ec4149
Autor:
Cibele Zanardi Esteves, Letícia de Aguiar Dias, Estela de Oliveira Lima, Diogo Noin de Oliveira, Carlos Fernando Odir Rodrigues Melo, Jeany Delafiori, Carla Cristina Souza Gomez, José Dirceu Ribeiro, Antônio Fernando Ribeiro, Carlos Emílio Levy, Rodrigo Ramos Catharino
Publikováno v:
Frontiers in Pediatrics, Vol 5 (2018)
BackgroundCystic fibrosis (CF) is a disabling genetic disease with an increased prevalence in European heritage populations. Currently, the most used technique for collection of CF samples and diagnosis is provided through uncomfortable tests, with u
Externí odkaz:
https://doaj.org/article/dec336c3670d4d35825c5bbb71bdc31c
Autor:
Taís Daiene Russo Hortencio, Roberto José Negrão Nogueira, Fernando Augusto de Lima Marson, Gabriel Hessel, José Dirceu Ribeiro, Antônio Fernando Ribeiro
Publikováno v:
Revista Paulista de Pediatria, Vol 33, Iss 1, Pp 3-11 (2015)
OBJECTIVE: The aim of this study was to evaluate by clinical and laboratory parameters how cystic fibrosis (CF) affects growth and nutritional status of children who were undergoing CF treatment but did not receive newborn screening. METHODS: A histo
Externí odkaz:
https://doaj.org/article/cec9a04e53124d8f870862b402b47ab0
Autor:
Alethéa Guimarães Faria, Fernando Augusto Lima Marson, Carla Cristina Souza Gomez, Maria de Fátima Servidoni, Antônio Fernando Ribeiro, José Dirceu Ribeiro
Publikováno v:
Frontiers in Pediatrics, Vol 5 (2017)
ObjectiveTo conduct a descriptive analysis of the sweat test (ST), associating ST results with epidemiological data, CFTR (cystic fibrosis transmembrane conductance regulator) mutations and reasons to indicate the ST, as well as correlating sweat sod
Externí odkaz:
https://doaj.org/article/5bb8a7b693904207af884ceb726a65ac
Autor:
Carmen Silvia Passos Lima, Manoela Marques Ortega, Fernando Augusto Lima Marson, Roberto Zulli, Antônio Fernando Ribeiro, Carmen Silvia Bertuzzo
Publikováno v:
Jornal Brasileiro de Pneumologia, Vol 38, Iss 1, Pp 50-56 (2012)
OBJETIVO: Determinar os efeitos que a mutação do gene cystic fibrosis transmembrane conductance regulator (CFTR) e da deleção dos genes glutationa S-transferase (GST) mu-1 (GSTM1) e teta-1 (GSTT1) têm na evolução clínica da fibrose cística (
Externí odkaz:
https://doaj.org/article/cb46057333c9438bb67279eab98b710d
Autor:
Fabíola Meister Pereira, Maria Ângela Gonçalves de Oliveira Ribeiro, Antônio Fernando Ribeiro, Adyléia Aparecida Dalbo Contrera Toro, Gabriel Hessel, José Dirceu Ribeiro
Publikováno v:
Jornal Brasileiro de Pneumologia, Vol 37, Iss 6, Pp 735-744 (2011)
OBJETIVO: Comparar pacientes com fibrose cística e indivíduos saudáveis quanto ao desempenho funcional no teste de caminhada de seis minutos (TC6). MÉTODOS: Estudo transversal e prospectivo, com indivíduos saudáveis e com fibrose cística de um
Externí odkaz:
https://doaj.org/article/bafcd93417c14c359bdc814262f96d17