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Article

Nasal airway ion transport is linked to the cystic fibrosis phenotype in adult patients.

Thorax - 1 Nov 2004

Fajac I, Hubert D, Guillemot D, Honoré I, Bienvenu T, Volter F, Dall'Ava-Santucci J, Dusser D J

Abstract excerpt

BACKGROUND: This study was conducted to determine whether the major nasal airway ion transport abnormalities in cystic fibrosis (that is, defective cAMP regulated chloride secretion and basal sodium hyperabsorption) are related to the clinical expression of cystic fibrosis and/or to the genotype....

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Topics

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Share to Analysis of Variance
Share to Chlorides
Share to Cystic Fibrosis

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Cystic Fibrosis Transmembrane Conductance Regulator

Share to Forced Expiratory Volume

Share to Ion Transport

Share to Membrane Potentials

Share to Nasal Mucosa

Source

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Identifiers

PMID: 15516474
DOI: 10.1136/thx.2003.020933
PMCID: PMC1746881

Genes

CFTR

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-15516474-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

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