Cargando…

Saliva as a potential tool for cystic fibrosis diagnosis

BACKGROUND: Saliva and sweat are modified by cystic fibrosis (CF). In both cases the chloride and sodium ion concentrations for healthy subjects and CF patients differ, this representing a possible alternative tool for CF diagnosis. In this context, the aim of this study was to compare the concentra...

Descripción completa

Detalles Bibliográficos
Autores principales:	Gonçalves, Aline Cristina, Marson, Fernando Augusto de Lima, Mendonça, Regina Maria de Holanda, Ribeiro, José Dirceu, Ribeiro, Antonio Fernando, Paschoal, Ilma Aparecida, Levy, Carlos Emílio
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2013
Materias:	Research
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3621375/ https://www.ncbi.nlm.nih.gov/pubmed/23510227 http://dx.doi.org/10.1186/1746-1596-8-46

Ejemplares similares

Volumetric capnography versus spirometry for the evaluation of pulmonary function in cystic fibrosis and allergic asthma()()
por: Almeida-Junior, Armando, et al.
Publicado: (2018)

Ventilatory abnormalities in patients with cystic fibrosis undergoing the submaximal treadmill exercise test
por: Parazzi, Paloma Lopes Francisco, et al.
Publicado: (2015)

Cystic fibrosis transmembrane conductance regulator mutations at a referral center for cystic fibrosis
por: Coutinho, Cyntia Arivabeni de Araújo Correia, et al.
Publicado: (2013)

Screening for F508del as a first step in the molecular diagnosis of cystic fibrosis,
por: Marson, Fernando Augusto de Lima, et al.
Publicado: (2013)

Genetic interaction of GSH metabolic pathway genes in cystic fibrosis
por: Marson, Fernando Augusto de Lima, et al.
Publicado: (2013)

Polymorphisms in the glutathione pathway modulate cystic fibrosis severity: a cross-sectional study
por: Marson, Fernando Augusto de Lima, et al.
Publicado: (2014)

Can continuous glucose monitoring predict cystic fibrosis-related diabetes and worse clinical outcome?
por: Zorron, Mariana, et al.
Publicado: (2022)

Sweat test and cystic fibrosis: overview of test performance at public and private centers in the state of São Paulo, Brazil
por: Servidoni, Maria Fátima, et al.
Publicado: (2017)

Association of growth and nutritional parameters with pulmonary function in cystic fibrosis: a literature review
por: Mauch, Renan Marrichi, et al.
Publicado: (2016)

Nasal Potential Difference in Cystic Fibrosis considering Severe CFTR Mutations
por: Ng, Ronny Tah Yen, et al.
Publicado: (2015)

Quality of sweat test (ST) based on the proportion of sweat sodium (Na) and sweat chloride (Cl) as diagnostic parameter of cystic fibrosis: are we on the right way?
por: Faria, Alethéa Guimarães, et al.
Publicado: (2016)

Erratum to: Quality of sweat test (ST) based on the proportion of sweat sodium (Na) and sweat chloride (Cl) as diagnostic parameter of cystic fibrosis: are we on the right way?
por: Faria, Alethéa Guimarães, et al.
Publicado: (2017)

Demographic, clinical, and laboratory parameters of cystic fibrosis during the last two decades: a comparative analysis
por: Marson, Fernando Augusto de Lima, et al.
Publicado: (2015)

Lung ultrasound assessment of response to antibiotic therapy in cystic fibrosis exacerbations: a study of two cases
por: Peixoto, Andressa Oliveira, et al.
Publicado: (2019)

Factors impacting the growth and nutritional status of cystic fibrosis patients younger than 10 years of age who did not undergo neonatal screening
por: Hortencio, Taís Daiene Russo, et al.
Publicado: (2015)

The relationship between physical functional capacity and lung function in obese children and adolescents
por: Ferreira, Mariana Simões, et al.
Publicado: (2014)

Evaluation of continuous constant current and continuous pulsed current in sweat induction for cystic fibrosis diagnosis
por: Gomez, Carla Cristina Souza, et al.
Publicado: (2018)

Combined multi-channel intraluminal impedance measurement and pHmetry in the detection of gastroesophageal reflux disease in children with cystic fibrosis
por: Gonçalves, Emília da Silva, et al.
Publicado: (2022)

Cost of precision medicine at a referral center for cystic fibrosis
por: Marson, Fernando Augusto Lima
Publicado: (2020)

Association between the IVS4G > T mutation in the TCF7L2 gene and susceptibility to diabetes in cystic fibrosis patients
por: Furgeri, Daniela Tenório, et al.
Publicado: (2012)

Personalized or Precision Medicine? The Example of Cystic Fibrosis
por: Marson, Fernando A. L., et al.
Publicado: (2017)

Novel, rare and common pathogenic variants in the CFTR gene screened by high-throughput sequencing technology and predicted by in silico tools
por: Pereira, Stéphanie Villa-Nova, et al.
Publicado: (2019)

Insulin therapy in patients with cystic fibrosis in the pre-diabetes stage: a systematic review
por: Pu, Mariana Zorrón Mei Hsia, et al.
Publicado: (2016)

Skin Biomarkers for Cystic Fibrosis: A Potential Non-Invasive Approach for Patient Screening
por: Esteves, Cibele Zanardi, et al.
Publicado: (2018)

Epidemiological aspects of and risk factors for wheezing in the first year of life
por: Fogaça, Hamilton Rosendo, et al.
Publicado: (2014)

Brazilian consensus on non-cystic fibrosis bronchiectasis
por: Pereira, Mônica Corso, et al.
Publicado: (2019)

Assessment of IgG antibodies to Pseudomonas aeruginosa in patients with cystic fibrosis by an enzyme-linked immunosorbent assay (ELISA)
por: Mauch, Renan Marrichi, et al.
Publicado: (2014)

Cystic Fibrosis: A Descriptive Analysis of Deaths in a Two-Decade Period in Brazil According to Age, Race, and Sex
por: de Azevedo, Luan Victor Frota, et al.
Publicado: (2023)

Polymorphisms in ADRB2 gene can modulate the response to bronchodilators and the severity of cystic fibrosis
por: Marson, Fernando A L, et al.
Publicado: (2012)

Cross-sectional evaluation of the saccharin transit time test for primary ciliary dyskinesia: did we discard this tool too soon?
por: Toro, Mariana Dalbo Contrera, et al.
Publicado: (2023)

Ventilatory Efficiency in Children and Adolescents: A Systematic Review
por: Parazzi, Paloma Lopes Francisco, et al.
Publicado: (2015)

Pseudomonas aeruginosa infection in patients with cystic fibrosis: scientific evidence regarding clinical impact, diagnosis, and treatment
por: da Silva, Luiz Vicente Ribeiro Ferreira, et al.
Publicado: (2013)

The ACE gene D/I polymorphism as a modulator of severity of cystic fibrosis
por: Marson, Fernando A L, et al.
Publicado: (2012)

Asthma: Gln27Glu and Arg16Gly polymorphisms of the beta2-adrenergic receptor gene as risk factors
por: de Paiva, Ana Carolina Zimiani, et al.
Publicado: (2014)

Thirty Years of Sweat Chloride Testing at One Referral Center
por: Faria, Alethéa Guimarães, et al.
Publicado: (2017)

Association between clinical variables related to asthma in schoolchildren born with very low birth weight with and without bronchopulmonary dysplasia
por: Gonçalves, Emília da Silva, et al.
Publicado: (2016)

MON-LB114 CGM in Cystic Fibrosis Patients to Predict Cystic Fibrosis-Related Diabetes Onset
por: Mei Hsia Pu, Mariana Zorron, et al.
Publicado: (2020)

Epidemiological Profile of Hospitalized Patients with Cystic Fibrosis in Brazil Due to Severe Acute Respiratory Infection during the COVID-19 Pandemic and a Systematic Review of Worldwide COVID-19 in Those with Cystic Fibrosis
por: Marques, Leonardo Souza, et al.
Publicado: (2023)

Brazilian guidelines for the diagnosis and treatment of cystic fibrosis
por: Athanazio, Rodrigo Abensur, et al.
Publicado: (2017)

SLC23A2-05 (rs4987219) and KRAS-LCS6 (rs61764370) polymorphisms in patients with squamous cell carcinoma of the head and neck
por: SANTIAGO, MARÍLIA BUENO, et al.
Publicado: (2014)

Cannot write session to /tmp/vufind_sessions/sess_p95d5fc3jps16a7m9h8l4sh8ci