The European MultiPartner IPF registry (EMPIRE): validating long-term prognostic factors in idiopathic pulmonary fibrosis
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1465-993X
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
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The European MultiPartner IPF registry (EMPIRE): validating long-term prognostic factors in idiopathic pulmonary fibrosis ; volume:21 ; number:1 ; day:8 ; month:1 ; year:2020 ; pages:1-9 ; date:12.2020
Respiratory research ; 21, Heft 1 (8.1.2020), 1-9, 12.2020
- Creator
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Tran, Tanja
Šterclová, Martina
Mogulkoc, Nesrin
Lewandowska, Katarzyna
Müller, Veronika
Hájková, Marta
Kramer, Mordechai R.
Jovanović, Dragana
Tekavec-Trkanjec, Jasna
Studnicka, Michael
Stoeva, Natalia
Hejduk, Karel
Dušek, Ladislav
Suissa, Samy
Vašáková, Martina
- Contributor
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SpringerLink (Online service)
- DOI
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10.1186/s12931-019-1271-z
- URN
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urn:nbn:de:101:1-2020041408080967153387
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 11:01 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Tran, Tanja
- Šterclová, Martina
- Mogulkoc, Nesrin
- Lewandowska, Katarzyna
- Müller, Veronika
- Hájková, Marta
- Kramer, Mordechai R.
- Jovanović, Dragana
- Tekavec-Trkanjec, Jasna
- Studnicka, Michael
- Stoeva, Natalia
- Hejduk, Karel
- Dušek, Ladislav
- Suissa, Samy
- Vašáková, Martina
- SpringerLink (Online service)
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Disease progression in idiopathic pulmonary fibrosis with mild physiological impairment: analysis from the Australian IPF registry
The European IPF registry (eurIPFreg): baseline characteristics and survival of patients with idiopathic pulmonary fibrosis
Health related quality of life in patients with idiopathic pulmonary fibrosis in clinical practice: insights-IPF registry
Baseline characteristics and survival of patients of idiopathic pulmonary fibrosis: a longitudinal analysis of the Swedish IPF Registry
Clinical characteristics of patients with familial idiopathic pulmonary fibrosis (f-IPF)
Predictors of death or lung transplant after a diagnosis of idiopathic pulmonary fibrosis: insights from the IPF-PRO Registry
Circulating matrix metalloproteinases and tissue metalloproteinase inhibitors in patients with idiopathic pulmonary fibrosis in the multicenter IPF-PRO Registry cohort
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Circulating metabolic profile in idiopathic pulmonary fibrosis: data from the IPF-PRO Registry
Peripheral blood proteomic profiling of idiopathic pulmonary fibrosis biomarkers in the multicentre IPF-PRO Registry
MiR-608 overexpression in idiopathic pulmonary fibrosis (IPF)
Clinical Outcomes of Patients with Combined Idiopathic Pulmonary Fibrosis and Emphysema in the IPF-PRO Registry
Disease progression in idiopathic pulmonary fibrosis with mild physiological impairment: analysis from the Australian IPF registry
The European IPF registry (eurIPFreg): baseline characteristics and survival of patients with idiopathic pulmonary fibrosis
Health related quality of life in patients with idiopathic pulmonary fibrosis in clinical practice: insights-IPF registry
Baseline characteristics and survival of patients of idiopathic pulmonary fibrosis: a longitudinal analysis of the Swedish IPF Registry
Clinical characteristics of patients with familial idiopathic pulmonary fibrosis (f-IPF)
Predictors of death or lung transplant after a diagnosis of idiopathic pulmonary fibrosis: insights from the IPF-PRO Registry
Circulating matrix metalloproteinases and tissue metalloproteinase inhibitors in patients with idiopathic pulmonary fibrosis in the multicenter IPF-PRO Registry cohort
Association of Circulating Proteins with Death or Lung Transplant in Patients with Idiopathic Pulmonary Fibrosis in the IPF-PRO Registry Cohort
Circulating metabolic profile in idiopathic pulmonary fibrosis: data from the IPF-PRO Registry
Peripheral blood proteomic profiling of idiopathic pulmonary fibrosis biomarkers in the multicentre IPF-PRO Registry
MiR-608 overexpression in idiopathic pulmonary fibrosis (IPF)
Clinical Outcomes of Patients with Combined Idiopathic Pulmonary Fibrosis and Emphysema in the IPF-PRO Registry
Disease progression in idiopathic pulmonary fibrosis with mild physiological impairment: analysis from the Australian IPF registry
The European IPF registry (eurIPFreg): baseline characteristics and survival of patients with idiopathic pulmonary fibrosis
Health related quality of life in patients with idiopathic pulmonary fibrosis in clinical practice: insights-IPF registry
Baseline characteristics and survival of patients of idiopathic pulmonary fibrosis: a longitudinal analysis of the Swedish IPF Registry
Clinical characteristics of patients with familial idiopathic pulmonary fibrosis (f-IPF)
Predictors of death or lung transplant after a diagnosis of idiopathic pulmonary fibrosis: insights from the IPF-PRO Registry
Circulating matrix metalloproteinases and tissue metalloproteinase inhibitors in patients with idiopathic pulmonary fibrosis in the multicenter IPF-PRO Registry cohort