Search Results - "Ribeiro, J.D"
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Applicability of lung ultrasound in COVID-19 diagnosis and evaluation of the disease progression: A systematic review
Published in Pulmonology (01-11-2021)“…The COVID-19 pandemic originated in China and within about 4 months affected individuals all over the world. One of the limitations to the management of the…”
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The correlation between age and sweat chloride levels in sweat tests
Published in Revista portuguesa de pneumologia (English ed.) (01-07-2017)Get full text
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13 Saliva for newborn screening for CF
Published in Journal of cystic fibrosis (01-06-2017)Get full text
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WS10.3 Chloride in saliva and sweat in age-matched individuals with and without CF
Published in Journal of cystic fibrosis (01-06-2017)Get full text
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Impulse oscillometry, spirometry, and passive smoking in healthy children and adolescents
Published in Revista portuguesa de pneumologia (English ed.) (01-11-2017)“…AbstractObjectiveTo identify changes in the forced and quiet breathing parameters of lung function in healthy children and adolescents exposed to passive…”
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Association between oxygenation and ventilation indices with the time on invasive mechanical ventilation in infants
Published in Pulmonology (01-07-2018)“…AbstractBackgroundInvasive mechanical ventilation (IMV) is a common practice in pediatric intensive care unit (PICU). However, the role of oxygenation (OI) and…”
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Physical performance, quality of life and sexual satisfaction evaluation in adults with cystic fibrosis: An unexplored correlation
Published in Revista portuguesa de pneumologia (English ed.) (01-07-2017)“…AbstractObjectiveQuality of life (QOL), sexual satisfaction (SS) and physical performance have been assessed in the management of numerous chronic…”
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A negative screening of rare genetic variants in the ADIPOQ and STATH genes in cystic fibrosis
Published in Pulmonology (01-05-2020)“…The phenotypic variability in cystic fibrosis (CF) is widely recognized and modulated by environmental and genetic factors, including CFTR pathogenic variants…”
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63 Pseudomonas aeruginosa pulmonary infection in CF patients in a Brazilian reference center: Antibody response monitoring
Published in Journal of cystic fibrosis (01-06-2015)“…Objective The diagnosis of P. aeruginosa ( P.a .) pulmonary infection in CF is often difficult, due to the lack of a representative clinical specimen. In this…”
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103 Low prevalence of mycobacteria among Brazilian CF patients: possible explanations
Published in Journal of cystic fibrosis (01-06-2016)Get full text
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110 Pitfalls in the diagnosis of Aspergillus disease in a cohort of Brazilian CF patients
Published in Journal of cystic fibrosis (01-06-2016)Get full text
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360 Clinical evolution of cystic fibrosis in 20 years: Experience at a referral center
Published in Journal of cystic fibrosis (01-06-2013)Get full text
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WS20.5 Genetic interaction of NOS-1 and CFTR gene and its association with cystic fibrosis severity
Published in Journal of cystic fibrosis (01-06-2013)Get full text
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16 The −765G>C and 8473T>C polymorphism in COX2 gene and 57460C>T polymorphism in IFRD1 gene as modifiers of cystic fibrosis severity
Published in Journal of cystic fibrosis (01-06-2013)Get full text
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119 Diagnostic value of serum antibodies to Pseudomonas aeruginosa in patients with CF in a Brazilian referral center
Published in Journal of cystic fibrosis (01-06-2014)Get full text
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192 Volumetric capnography is correlated with spirometry in cystic fibrosis patients
Published in Journal of cystic fibrosis (01-06-2013)Get full text
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132 Anti-Pseudomonas aeruginosa IgG ELISA in a CF referral center in Brazil. Preliminary results
Published in Journal of cystic fibrosis (01-06-2013)Get full text
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WS8.6 Interaction of microorganisms modulating the cystic fibrosis clinical severity
Published in Journal of cystic fibrosis (01-06-2013)Get full text
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Correlation between parameters of volumetric capnography and spirometry during a submaximal exercise protocol on a treadmill in patients with cystic fibrosis and healthy controls
Published in Pulmonology (01-01-2019)“…Spirometry is the most frequently used test to evaluate the progression of lung damage in cystic fibrosis (CF). However, there has been low sensitivity in…”
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