Exhaled molecular profiles in the assessment of cystic fibrosis and primary ciliary dyskinesia-Reference-Cited by-同舟云学术

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Exhaled molecular profiles in the assessment of cystic fibrosis and primary ciliary dyskinesia

Published:2013-09 Issue:5 Volume:12 Page:454-460
ISSN:1569-1993
Container-title:Journal of Cystic Fibrosis
language:en
Short-container-title:Journal of Cystic Fibrosis

Author:

Paff T.,van der Schee M.P.,Daniels J.M.A.,Pals G.,Postmus P.E.,Sterk P.J.,Haarman E.G.

Funder

Stichting PCD Belangengroep

Publisher

Elsevier BV

Subject

Pulmonary and Respiratory Medicine,Pediatrics, Perinatology, and Child Health

Reference30 articles.

1. Primary ciliary dyskinesia: a consensus statement on diagnostic and treatment approaches in children;Barbato;Eur Respir J,2009

2. Longitudinal study of lung function in a cohort of primary ciliary dyskinesia;Ellerman;Eur Respir J,1997

3. Management of primary ciliary dyskinesia in European children: recommendations and clinical practice;Strippoli;Eur Respir J,2012

4. Pulmonary perspective cystic fibrosis pulmonary guidelines: treatment of pulmonary exacerbations;Flume;Am J Respir Crit Care Med,2009

5. Pathophysiology and management of pulmonary infections in cystic fibrosis;Gibson;Am J Respir Crit Care Med,2003

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4. Advancements and Prospects of Electronic Nose in Various Applications: A Comprehensive Review;Applied Sciences;2024-05-24

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