- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1465-993X
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Anmerkungen
-
online resource.
- Erschienen in
-
Pulmonary aspiration in preschool children with cystic fibrosis ; volume:19 ; number:1 ; day:17 ; month:12 ; year:2018 ; pages:1-3 ; date:12.2018
Respiratory research ; 19, Heft 1 (17.12.2018), 1-3, 12.2018
- Urheber
-
Clarke, D.
Gorman, I.
Ringholz, F.
McDermott, M.
Cox, DW
Greally, P.
Linnane, B.
Mc Nally, P.
- Beteiligte Personen und Organisationen
-
SpringerLink (Online service)
- DOI
-
10.1186/s12931-018-0954-1
- URN
-
urn:nbn:de:101:1-2019020522404205552676
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
14.08.2025, 10:56 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Clarke, D.
- Gorman, I.
- Ringholz, F.
- McDermott, M.
- Cox, DW
- Greally, P.
- Linnane, B.
- Mc Nally, P.
- SpringerLink (Online service)
Ähnliche Objekte (12)
Pulmonary exacerbations and clinical outcomes in a longitudinal cohort of infants and preschool children with cystic fibrosis
Cystic fibrosis
Cystic fibrosis pulmonary infections: lessons from around the world
Lung function imaging methods in Cystic Fibrosis pulmonary disease
Cystic fibrosis transmembrane conductance regulator (CFTR): beyond cystic fibrosis
Macrorheology of cystic fibrosis, chronic obstructive pulmonary disease & normal sputum
Mycobacterium chimaera pulmonary infection complicating cystic fibrosis: a case report
Lung ultrasound for the diagnosis of cystic fibrosis pulmonary exacerbation
Neuropeptides in asthma, chronic obstructive pulmonary disease and cystic fibrosis
Lack of correlation between pulmonary disease and cystic fibrosis transmembrane conductance regulator dysfunction in cystic fibrosis: a case report
Comparative microbiome analysis in cystic fibrosis and non-cystic fibrosis bronchiectasis
Effect of esomeprazole versus placebo on pulmonary exacerbations in cystic fibrosis
Pulmonary exacerbations and clinical outcomes in a longitudinal cohort of infants and preschool children with cystic fibrosis
Cystic fibrosis
Cystic fibrosis pulmonary infections: lessons from around the world
Lung function imaging methods in Cystic Fibrosis pulmonary disease
Cystic fibrosis transmembrane conductance regulator (CFTR): beyond cystic fibrosis
Macrorheology of cystic fibrosis, chronic obstructive pulmonary disease & normal sputum
Mycobacterium chimaera pulmonary infection complicating cystic fibrosis: a case report
Lung ultrasound for the diagnosis of cystic fibrosis pulmonary exacerbation
Neuropeptides in asthma, chronic obstructive pulmonary disease and cystic fibrosis
Lack of correlation between pulmonary disease and cystic fibrosis transmembrane conductance regulator dysfunction in cystic fibrosis: a case report
Comparative microbiome analysis in cystic fibrosis and non-cystic fibrosis bronchiectasis
Effect of esomeprazole versus placebo on pulmonary exacerbations in cystic fibrosis
Pulmonary exacerbations and clinical outcomes in a longitudinal cohort of infants and preschool children with cystic fibrosis
Cystic fibrosis
Cystic fibrosis pulmonary infections: lessons from around the world
Lung function imaging methods in Cystic Fibrosis pulmonary disease
Cystic fibrosis transmembrane conductance regulator (CFTR): beyond cystic fibrosis
Macrorheology of cystic fibrosis, chronic obstructive pulmonary disease & normal sputum
Mycobacterium chimaera pulmonary infection complicating cystic fibrosis: a case report
Lung ultrasound for the diagnosis of cystic fibrosis pulmonary exacerbation
Neuropeptides in asthma, chronic obstructive pulmonary disease and cystic fibrosis
Lack of correlation between pulmonary disease and cystic fibrosis transmembrane conductance regulator dysfunction in cystic fibrosis: a case report
Comparative microbiome analysis in cystic fibrosis and non-cystic fibrosis bronchiectasis