(Q47800271)

5 February 2018

title

Nasal airway ion transport and lung function in young people with cystic fibrosis (English)

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5 February 2018

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Helen L Wallace

1

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5 February 2018

Pierre M Barker

series ordinal

2

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5 February 2018

Kevin W Southern

series ordinal

3

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5 February 2018

language of work or name

English

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publication date

26 June 2003

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5 February 2018

American Journal of Respiratory and Critical Care Medicine

published in

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5 February 2018

volume

168

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5 February 2018

issue

5

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5 February 2018

page(s)

594-600

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5 February 2018

CFTR as a cAMP-dependent regulator of sodium channels

cites work

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200211-1302OC

Yes-associated protein 65 localizes p62(c-Yes) to the apical compartment of airway epithelia by association with EBP50

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200211-1302OC

Regulation of epithelial sodium channels by the cystic fibrosis transmembrane conductance regulator.

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200211-1302OC

Lower airway inflammation in infants and young children with cystic fibrosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200211-1302OC

'CFTR-opathies': disease phenotypes associated with cystic fibrosis transmembrane regulator gene mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200211-1302OC

Determinants of mild clinical symptoms in cystic fibrosis patients. Residual chloride secretion measured in rectal biopsies in relation to the genotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200211-1302OC

Genotype-phenotype relationships in cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200211-1302OC

Contribution of genetic factors other than CFTR to disease severity in cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200211-1302OC

Relationship between airway ion transport and a mild pulmonary disease mutation in CFTR.

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200211-1302OC

The chest radiograph in cystic fibrosis: a new scoring system compared with the Chrispin-Norman and Brasfield scores

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200211-1302OC

A modified technique for measurement of nasal transepithelial potential difference in infants

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200211-1302OC

Nasal application of the cationic liposome DC-Chol:DOPE does not alter ion transport, lung function or bacterial growth

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200211-1302OC

Longitudinal analysis of pulmonary function decline in patients with cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200211-1302OC

Factors associated with poor pulmonary function: cross-sectional analysis of data from the ERCF. European Epidemiologic Registry of Cystic Fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200211-1302OC

Measuring agreement in method comparison studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200211-1302OC

Nasal epithelium potential difference at high altitude (4,559 m): evidence for secretion

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200211-1302OC

Association of mannose-binding lectin gene heterogeneity with severity of lung disease and survival in cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200211-1302OC

Endothelial Nitric Oxide Synthase Variants in Cystic Fibrosis Lung Disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200211-1302OC

End-organ dysfunction in cystic fibrosis: association with angiotensin I converting enzyme and cytokine gene polymorphisms.

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200211-1302OC

Cystic fibrosis: gene therapy or preventive gene transfer?

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200211-1302OC

Correlation between nasal potential difference measurements, genotype and clinical condition in patients with cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200211-1302OC

10.1164/RCCM.200211-1302OC

21 January 2018

Identifiers

DOI

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5 February 2018

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5 February 2018