Cross‐talk between CFTR and sphingolipids in cystic fibrosis
Several lines of evidence shown that in cystic fibrosis the lack of the cystic fibrosis transmembrane conductance regulator (CFTR) is accompanied by changes in the plasma membrane composition of a bioactive class of lipids known as sphingolipids. Here, we depict a general overview of the literature related to the impact of the modifications of the ...
Dorina Dobi +6 more
wiley +1 more source
Fibrose cística e a triagem neonatal [PDF]
The clinical and diagnostic aspects of cystic fibrosis have been extensively reviewed, with an emphasis on neonatal screening. This systematic literature review involved a search for relevant contributions in the PubMed and SciELO databases.
FERNANDES, Maria I. M. +7 more
core +2 more sources
RESUMO Comparou-se a força muscular respiratória, qualidade de vida e capacidade funcional em adolescentes com fibrose cística com diferentes perfis bacteriológicos.
Rafaela Cerqueira Andrade +5 more
doaj +2 more sources
Results of nutritional intervention in children and adolescents with cystic fibrosis [PDF]
Objective: few studies have verified longitudinally the evolution of the nutritional status of patients with cystic fibrosis. The objective of this study is to follow the evolution of the nutritional status, body composition and energy consumption ...
Ancona-Lopez, Fabio +5 more
core +3 more sources
Cell therapy in pulmonary diseases: are there perspectives? [PDF]
A terapia celular poderia ser conceituada de forma ampla e genérica como o emprego de células para tratamento de doenças. Apesar de um número não tão expressivo de relatos tendo o pulmão como objeto de estudo na terapia celular em pacientes humanos, há ...
ALVES-DE-MORAES, Luis B. C. +6 more
core +1 more source
O impacto de primeiro ano de tratamento com dornase alfa nos parâmetros clínicos de pacientes com fibrose cística: estudo multicêntrico brasileiro [PDF]
OBJECTIVE:To describe the clinical impact of the first year treatment with dornase alfa, according to age groups, in a cohort of Brazilian Cystic Fibrosis (CF) patients.METHODS:The data on 152 eligible patients, from 16 CF reference centers, that ...
Adde, Fabíola Villac +4 more
core +4 more sources
Prevalência de doenças diagnosticadas pela triagem neonatal em uma região de Mato Grosso, Brasil
Objetivo: analisar a prevalência de doenças diagnosticadas pela triagem neonatal em uma região de Mato Grosso, Brasil. Método: estudo descritivo e quantitativo, com análise do rastreamento neonatal de 4057 recém-nascidos em dez municípios de Mato Grosso,
Kaynara Borges Oliveira +5 more
doaj +1 more source
The invisible patients: posttraumatic stress disorder in parents of individuals with cystic fibrosis [PDF]
BACKGROUND: Besides the growing acknowledgment of the relevance of posttraumatic stress disorder (PTSD) related to medical illness, there is no study in cystic fibrosis yet.
Cabizuca, Mariana +7 more
core +3 more sources
Towards Targeting the Aryl Hydrocarbon Receptor in Cystic Fibrosis
Tryptophan (trp) metabolism is an important regulatory component of gut mucosal homeostasis and the microbiome. Metabolic pathways targeting the trp can lead to a myriad of metabolites, of both host and microbial origins, some of which act as endogenous low‐affinity ligands for the aryl hydrocarbon receptor (AhR), a cytosolic, ligand‐operated ...
Matteo Puccetti +13 more
wiley +1 more source
The Mast Cell‐Aryl Hydrocarbon Receptor Interplay at the Host‐Microbe Interface
Mast cells are increasingly being recognized as crucial cells in the response of the organism to environmental agents. Interestingly, the ability of mast cells to sense and respond to external cues is modulated by the microenvironment that surrounds mast cells and influences their differentiation.
Claudio Costantini +13 more
wiley +1 more source

