Zobrazeno 1 - 10
of 190
pro vyhledávání: '"Paulo de tarso Roth Dalcin"'
Autor:
Heryk Motta, Júlia Catarina Vieira Reuwsaat, Fernanda Cortez Lopes, Graciele Viezzer, Fabiana Caroline Zempulski Volpato, Afonso Luís Barth, Paulo de Tarso Roth Dalcin, Charley Christian Staats, Marilene Henning Vainstein, Lívia Kmetzsch
Publikováno v:
Respiratory Research, Vol 25, Iss 1, Pp 1-18 (2024)
Abstract Background Bronchiectasis is a condition characterized by abnormal and irreversible bronchial dilation resulting from lung tissue damage and can be categorized into two main groups: cystic fibrosis (CF) and non-CF bronchiectasis (NCFB). Both
Externí odkaz:
https://doaj.org/article/60907b5620af4b29aae850e66c0493fc
Autor:
Vanessa Albano Barcellos, Vanessa Cristina Hartmann dos Santos, Maria Ângela Fontoura Moreira, Paulo de Tarso Roth Dalcin
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-9 (2023)
Abstract Asthma control and health related quality of life are an important goal of asthma management, but their association with sputum eosinophilic inflammation has been less firmly established. To investigate the relationship of asthma control and
Externí odkaz:
https://doaj.org/article/2d75f9030a5046adab01a2a6ff740922
Publikováno v:
Jornal Brasileiro de Pneumologia, Vol 50, Iss 2 (2024)
Externí odkaz:
https://doaj.org/article/1cc7dbc72db14fcfb9ce499ed6586cd6
Autor:
Rodrigo Abensur Athanazio, Suzana Erico Tanni, Juliana Ferreira, Paulo de Tarso Roth Dalcin, Marcelo B de Fuccio, Concetta Esposito, Mariane Gonçalves Martynychen Canan, Liana Sousa Coelho, Mônica de Cássia Firmida, Marina Buarque de Almeida, Paulo José Cauduro Marostica, Luciana de Freitas Velloso Monte, Edna Lúcia Souza, Leonardo Araujo Pinto, Samia Zahi Rached, Verônica Stasiak Bednarczuk de Oliveira, Carlos Antonio Riedi, Luiz Vicente Ribeiro Ferreira da Silva Filho
Publikováno v:
Jornal Brasileiro de Pneumologia, Vol 49, Iss 2 (2023)
ABSTRACT Cystic fibrosis (CF) is a genetic disease that results in dysfunction of the CF transmembrane conductance regulator (CFTR) protein, which is a chloride and bicarbonate channel expressed in the apical portion of epithelial cells of various or
Externí odkaz:
https://doaj.org/article/2ee12dd8b3bd413899822534cd8fd4b1
Autor:
Vanessa de Souza Vieira, Taiane dos Santos Feiten, Renata Salatti Ferrari, Paulo de Tarso Roth Dalcin, Bruna Ziegler
Publikováno v:
Jornal de Pediatria, Vol 98, Iss 1, Pp 33-38 (2022)
Objective: In this present study, the authors evaluated the predictive factors for adverse maternal-fetal outcomes in pregnancies of women with cystic fibrosis (CF). Patients were followed up by a referral center for adults in southern Brazil. Method
Externí odkaz:
https://doaj.org/article/cf2e6ac6b5c54fb9ae0ee33114678dcb
Autor:
Cristiane Christ Camargo, Letícia Bauer Jacobsen, Jaqueline Wilsmann, Michelle Nunes Silveira, Bruna Ziegler, Elis de Pellegrin Rossi, Carla Tatiana Oliveira, Paulo de Tarso Roth Dalcin
Publikováno v:
Jornal Brasileiro de Pneumologia, Vol 48, Iss 6 (2022)
ABSTRACT Objective: There is still limited information on the clinical characteristics and outcomes of cystic fibrosis (CF) patients with COVID-19 in Brazil. The objective of this study was to describe the cumulative incidence of COVID-19 in CF patie
Externí odkaz:
https://doaj.org/article/e0d06ee505ce46eb903abee0102948b6
Publikováno v:
BMC Pulmonary Medicine, Vol 20, Iss 1, Pp 1-8 (2020)
Abstract Background Advanced lung disease in adult cystic fibrosis (CF) drives most clinical care requirements. The aim was to evaluate outcome (time to death while in the study) in a cohort of adult CF patients with severe lung disease, and to deter
Externí odkaz:
https://doaj.org/article/a1446fe8d79e45ed9584689469b75356
Autor:
Cristina Carra Forte, Gabriele Carra Forte, Maria Luiza Torres Hennemann, Luiza Tweedie Preto, Jussara Carnevale Almeida, Paulo de Tarso Roth Dalcin, Raquel Canuto
Publikováno v:
Clinical and Biomedical Research, Vol 41, Iss 4 (2021)
Objectives: To assess the association between dietary patterns, nutritional status and asthma control in patients treated at a referral center for asthma in Porto Alegre, Brazil. Methods: This is a cross-sectional study with 198 adult asthma patients
Externí odkaz:
https://doaj.org/article/4ea4f782d89d4590bb14cbb7f8b73e55
Autor:
Marília Amaral Peixoto da Silveira, Patrícia Amaral Peixoto da Silveira, Flávia Gabe Beltrami, Leandro Armani Scaffaro, Paulo de Tarso Roth Dalcin
Publikováno v:
Jornal Brasileiro de Pneumologia, Vol 47, Iss 4 (2021)
ABSTRACT Objective: Massive hemoptysis is one of the most serious complications in patients with cystic fibrosis (CF). This study aimed to evaluate the hemoptysis-free period following bronchial and non-bronchial artery embolization (BAE/non-BAE) in
Externí odkaz:
https://doaj.org/article/3fe7c8f42300460cb53ccaf2b4f57fa4
Autor:
Thaís Peruch, Taiane dos Santos Feiten, Josani da Silva Flores, Paulo de Tarso Roth Dalcin, Bruna Ziegler
Publikováno v:
Clinical and Biomedical Research, Vol 40, Iss 2 (2021)
Introduction: Inhalation therapy is a crucial part of the cystic fibrosis (CF) treatment regimen. Drugs that assist in mucociliary clearance and inhaled antibiotics are used by most patients. Methods: This is a cross-sectional study where patients wi
Externí odkaz:
https://doaj.org/article/aaf66b58bbda46bd98343d9fe1712e1f