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The therapy of idiopathic pulmonary fibrosis: what is next?

Vivien Somogyi, Nazia Chaudhuri, Sebastiano Emanuele Torrisi, Nicolas Kahn, Veronika Müller, Michael Kreuter
European Respiratory Review 2019 28: 190021; DOI: 10.1183/16000617.0021-2019
Vivien Somogyi
1Center for Interstitial and Rare Lung Diseases, Pneumology, Thoraxklinik, University of Heidelberg, German Center for Lung Research (DZL), Heidelberg, Germany
2Dept of Pulmonology, Semmelweis University, Budapest, Hungary
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Nazia Chaudhuri
3Manchester University NHS Foundation Trust, Wythenshawe Hospital, Manchester, UK
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Sebastiano Emanuele Torrisi
1Center for Interstitial and Rare Lung Diseases, Pneumology, Thoraxklinik, University of Heidelberg, German Center for Lung Research (DZL), Heidelberg, Germany
4Regional Referral Centre for Rare Lung Diseases, University Hospital “Policlinico”, Dept of Clinical and Experimental Medicine, University of Catania, Catania, Italy
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Nicolas Kahn
1Center for Interstitial and Rare Lung Diseases, Pneumology, Thoraxklinik, University of Heidelberg, German Center for Lung Research (DZL), Heidelberg, Germany
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Veronika Müller
2Dept of Pulmonology, Semmelweis University, Budapest, Hungary
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Michael Kreuter
1Center for Interstitial and Rare Lung Diseases, Pneumology, Thoraxklinik, University of Heidelberg, German Center for Lung Research (DZL), Heidelberg, Germany
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  • For correspondence: kreuter@uni-heidelberg.de
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Article Information

vol. 28 no. 153
DOI 
https://doi.org/10.1183/16000617.0021-2019
PubMed 
31484664

Published By 
European Respiratory Society
Print ISSN 
0905-9180
Online ISSN 
1600-0617
History 
  • Received February 27, 2019
  • Accepted May 16, 2019
  • Published online September 4, 2019.

Copyright & Usage 
Copyright ©ERS 2019. This article is open access and distributed under the terms of the Creative Commons Attribution Non-Commercial Licence 4.0.

Author Information

  1. Vivien Somogyi1,2,
  2. Nazia Chaudhuri3,
  3. Sebastiano Emanuele Torrisi1,4,
  4. Nicolas Kahn1,
  5. Veronika Müller2 and
  6. Michael Kreuter1⇑
  1. 1Center for Interstitial and Rare Lung Diseases, Pneumology, Thoraxklinik, University of Heidelberg, German Center for Lung Research (DZL), Heidelberg, Germany
  2. 2Dept of Pulmonology, Semmelweis University, Budapest, Hungary
  3. 3Manchester University NHS Foundation Trust, Wythenshawe Hospital, Manchester, UK
  4. 4Regional Referral Centre for Rare Lung Diseases, University Hospital “Policlinico”, Dept of Clinical and Experimental Medicine, University of Catania, Catania, Italy
  1. Michael Kreuter, Center for Interstitial and Rare Lung Diseases, Thoraxklinik, University of Heidelberg, German Center for Lung Research (DZL), Heidelberg, Germany. E-mail: kreuter{at}uni-heidelberg.de
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Vol 28 Issue 153 Table of Contents
European Respiratory Review: 28 (153)
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The therapy of idiopathic pulmonary fibrosis: what is next?
Vivien Somogyi, Nazia Chaudhuri, Sebastiano Emanuele Torrisi, Nicolas Kahn, Veronika Müller, Michael Kreuter
European Respiratory Review Sep 2019, 28 (153) 190021; DOI: 10.1183/16000617.0021-2019

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The therapy of idiopathic pulmonary fibrosis: what is next?
Vivien Somogyi, Nazia Chaudhuri, Sebastiano Emanuele Torrisi, Nicolas Kahn, Veronika Müller, Michael Kreuter
European Respiratory Review Sep 2019, 28 (153) 190021; DOI: 10.1183/16000617.0021-2019
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  • Article
    • Abstract
    • Abstract
    • Introduction
    • ABCDE and future approaches in IPF
    • Biomarkers guiding therapy
    • New approaches in drug treatment in IPF
    • Developments in lung transplantation
    • Pulmonary rehabilitation
    • New ways to approach palliative intervention
    • Treatment of comorbidities
    • Urgent unmet need for AE-IPF
    • Conclusions
    • Footnotes
    • References
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  • Info & Metrics
  • PDF

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  • Pulmonary vascular disease
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