Cargando…

Association of growth and nutritional parameters with pulmonary function in cystic fibrosis: a literature review

OBJECTIVE: To review the literature addressing the relationship of growth and nutritional parameters with pulmonary function in pediatric patients with cystic fibrosis. DATA SOURCE: A collection of articles published in the last 15 years in English, Portuguese and Spanish was made by research in ele...

Descripción completa

Detalles Bibliográficos
Autores principales:	Mauch, Renan Marrichi, Kmit, Arthur Henrique Pezzo, Marson, Fernando Augusto de Lima, Levy, Carlos Emilio, Barros-Filho, Antonio de Azevedo, Ribeiro, José Dirceu
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Sociedade de Pediatria de São Paulo 2016
Materias:	Review Articles
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5176073/ https://www.ncbi.nlm.nih.gov/pubmed/27181343 http://dx.doi.org/10.1016/j.rppede.2016.02.001

Ejemplares similares

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)

Saliva as a potential tool for cystic fibrosis diagnosis
por: Gonçalves, Aline Cristina, et al.
Publicado: (2013)

Cystic fibrosis transmembrane conductance regulator mutations at a referral center for cystic fibrosis
por: Coutinho, Cyntia Arivabeni de Araújo Correia, 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)

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)

One Year of Coronavirus Disease 2019 (COVID-19) in Brazil: A Political and Social Overview
por: Boschiero, Matheus Negri, et al.
Publicado: (2021)

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)

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

Adaptive Immune Response to Mycobacterium abscessus Complex (MABSC) in Cystic Fibrosis and the Implications of Cross-Reactivity
por: Mauch, Renan Marrichi, et al.
Publicado: (2022)

Frequency of respiratory pathogens other than SARS-CoV-2 detected during COVID-19 testing
por: Boschiero, Matheus Negri, et al.
Publicado: (2022)

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

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

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

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

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)

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)

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

Cross-talk of inflammatory mediators and airway epithelium reveals the cystic fibrosis transmembrane conductance regulator as a major target
por: Simões, Filipa B., et al.
Publicado: (2021)

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)

Challenges in the identification of Chryseobacterium indologenes and Elizabethkingia meningoseptica in cases of nosocomial infections and patients with cystic fibrosis
por: de Carvalho Filho, É.B., et al.
Publicado: (2017)

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)

Sphingobacterium respiratory tract infection in patients with cystic fibrosis
por: Lambiase, Antonietta, et al.
Publicado: (2009)

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)

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

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)

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)

Brazilian Guidelines for Nutrition in Cystic Fibrosis
por: Neri, Lenycia de Cassya Lopes, et al.
Publicado: (2022)

Measurements of CFTR-Mediated Cl(−) Secretion in Human Rectal Biopsies Constitute a Robust Biomarker for Cystic Fibrosis Diagnosis and Prognosis
por: Sousa, Marisa, et al.
Publicado: (2012)

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

Microbiology of airway disease in a cohort of patients with Cystic Fibrosis
por: Lambiase, Antonietta, et al.
Publicado: (2006)

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)

Achromobacter xylosoxidans respiratory tract infection in cystic fibrosis patients
por: Lambiase, A., et al.
Publicado: (2011)

Microbiological contamination of nebulizers used by cystic fibrosis patients: an underestimated problem
por: Riquena, Barbara, et al.
Publicado: (2019)

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)

EVALUATION OF NUTRITIONAL STATUS IN PATIENTS WITH CYSTIC FIBROSIS ACCORDING TO AGE GROUP
por: Neri, Lenycia de Cassya Lopes, 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)

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)

Zinc Nutritional Status in Patients with Cystic Fibrosis
por: Escobedo Monge, Marlene Fabiola, et al.
Publicado: (2019)

Cannot write session to /tmp/vufind_sessions/sess_1ctm2ps78k6dcicqnl3bde4tnt