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ICOS protects against mortality from acute lung injury through activation of IL-5 + ILC2s

Mucosal immunology, 2018-01, Vol.11 (1), p.61-70

2018

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Prevalence of hiatal hernia by blinded multidetector CT in patients with idiopathic pulmonary fibrosis

The European respiratory journal, 2012-02, Vol.39 (2), p.344-351

2012

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Levels of soluble human leukocyte antigen-G are increased in asthmatic airways

The European respiratory journal, 2010-04, Vol.35 (4), p.925-927

2010

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Anti-acid treatment and disease progression in idiopathic pulmonary fibrosis: an analysis of data from three randomised controlled trials

The lancet respiratory medicine, 2013-07, Vol.1 (5), p.369-376

2013

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A Controlled Trial of Sildenafil in Advanced Idiopathic Pulmonary Fibrosis

The New England journal of medicine, 2010-08, Vol.363 (7), p.620-628

2010

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Sexualisierte Gewalt in kirchlichen Kontexten | Sexual Violence in the Context of the Church: Neue interdisziplinare Perspektiven | New Interdisciplinary Perspectives

2021

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C101 IPF: CLINICAL STUDIES, THERAPEUTICS, AND MORE II: Prepabel: A Bioinformatic Tool For Preprocessing Imputed Genotype Dosage Data For Survival Analyses

American journal of respiratory and critical care medicine, 2017-01, Vol.195

2017

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C38 UNDERSTANDING THERAPEUTICS IN IPF: Cardiovascular Safety Of Nintedanib In Subgroups By Cardiovascular Risk At Baseline In The Tomorrow And Inpulsis Trials

American journal of respiratory and critical care medicine, 2017-01, Vol.195

2017

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P168 Safety and tolerability of nintedanib in patients with idiopathic pulmonary fibrosis (IPF): one-year data from post-marketing surveillance in the united states

Thorax, 2016-12, Vol.71 (Suppl 3), p.A175-A175

2016

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Lung microbiome and disease progression in idiopathic pulmonary fibrosis: an analysis of the COMET study

The lancet respiratory medicine, 2014-07, Vol.2 (7), p.548-556

2014

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Suspected acute exacerbation of idiopathic pulmonary fibrosis as an outcome measure in clinical trials

Respiratory research, 2013-07, Vol.14 (1), p.73-73

2013

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A40 CONNECTIVE TISSUE DISEASE RELATED INTERSTITIAL LUNG DISEASE: RISK FACTORS, DIAGNOSIS, AND OUTCOMES: Rheumatoid Arthritis-Associated Interstitial Lung Disease: Risk Factors For Disease Progression

American journal of respiratory and critical care medicine, 2014-01, Vol.189, p.1

2014

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A103 IPF: MORE ABOUT THERAPY AND OUTCOMES: Safety And Tolerability Of Nintedanib In Patients With Idiopathic Pulmonary Fibrosis (ipf): One-Year Data From Post-Marketing Surveillance In The United States

American journal of respiratory and critical care medicine, 2016-01, Vol.193, p.1

2016

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A42 NEW DEVELOPMENTS IN ILD RESEARCH: Regional Heterogeneity In Autoimmune Features Among Patients With Fibrotic Interstitial Lung Disease

American journal of respiratory and critical care medicine, 2017-01, Vol.195

2017

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Identification of Diagnostic Criteria for Chronic Hypersensitivity Pneumonitis: An International Modified Delphi Survey

American journal of respiratory and critical care medicine, 2018-04, Vol.197 (8), p.1036-1044

2018

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A93 EXPLORING THE HUMAN RESPIRATORY ADAPTIVE IMMUNE RESPONSE: Ccr4-Expressing Cd4+ T Cells Are Increased In Lungs Of Patients With Idiopathic Pulmonary Fibrosis And Correlate With Lung Function

American journal of respiratory and critical care medicine, 2016-01, Vol.193, p.1

2016

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B110 NOVEL THERAPIES AND TARGETS IN FIBROSIS: Non Circulating Pulmonary Resident Memory T Cells Can Be Identified And Demonstrate Activated Phenotypes In Idiopathic Pulmonary Fibrosis

American journal of respiratory and critical care medicine, 2016-01, Vol.193, p.1

2016

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D28 THE WEB OF OMICS: DNA, RNA, AND PROTEIN MODIFICATIONS: Dna Methylation And Epigenetic Age Characterize Molecular Differences Between Idiopathic Pulmonary Fibrosis And COPD

American journal of respiratory and critical care medicine, 2017-01, Vol.195

2017

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A93 ROLE OF ADAPTIVE IMMUNITY IN LUNG DISEASE: Stratification Of Idiopathic Pulmonary Fibrosis Survival By Icos And Cd28 Surface Expression On T Cells

American journal of respiratory and critical care medicine, 2017-01, Vol.195

2017

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A75 BIG AND BIGGER (DATA): OMICS AND BIOMARKERS OF LUNG DISEASES: A Genome-Wide Network Analysis Of Gene Polymorphisms Associated With Idiopathic Pulmonary Fibrosis Susceptibility

American journal of respiratory and critical care medicine, 2017-01, Vol.195

2017

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Imatinib Treatment for Idiopathic Pulmonary Fibrosis: Randomized Placebo-controlled Trial Results

American journal of respiratory and critical care medicine, 2010-03, Vol.181 (6), p.604-610

2010

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D103 DR. "NOBODY CAN DIAGNOSE INTERSTITIAL LUNG DISEASE ALONE": MULTIDISCIPLINARY EVALUATION OF INTERSTITIAL LUNG DISEASE: A Novel, Blood-Based Diagnostic Gene Signature For Rheumatoid-Arthritis Interstitial Lung Disease

American journal of respiratory and critical care medicine, 2014-01, Vol.189, p.1

2014

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A41 INTERSTITIAL LUNG DISEASE: RISK FACTORS AND OUTCOMES: Hypothyroidism In Patients With Idiopathic Pulmonary Fibrosis

American journal of respiratory and critical care medicine, 2014-01, Vol.189, p.1

2014

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C61 SURVEYING THE LANDSCAPE: OMIC APPROACHES TO STUDY LUNG DISEASE: Peripheral Blood Gene Signature Distinguishes Sarcoidosis From Idiopathic Pulmonary Fibrosis

American journal of respiratory and critical care medicine, 2014-01, Vol.189, p.1

2014

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B57 GENE REGULATION: MIRNAS AND EPIGENETICS: Micrornas Regulate The Expression Of Tollip Gene Involved In Idiopathic Pulmonary Fibrosis Susceptibility

American journal of respiratory and critical care medicine, 2015-01, Vol.191, p.1

2015

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ICOS protects against mortality from acute lung injury through activation of IL-5 + ILC2s

Prevalence of hiatal hernia by blinded multidetector CT in patients with idiopathic pulmonary fibrosis

Levels of soluble human leukocyte antigen-G are increased in asthmatic airways

Anti-acid treatment and disease progression in idiopathic pulmonary fibrosis: an analysis of data from three randomised controlled trials

A Controlled Trial of Sildenafil in Advanced Idiopathic Pulmonary Fibrosis

Sexualisierte Gewalt in kirchlichen Kontexten | Sexual Violence in the Context of the Church: Neue interdisziplinare Perspektiven | New Interdisciplinary Perspectives

C101 IPF: CLINICAL STUDIES, THERAPEUTICS, AND MORE II: Prepabel: A Bioinformatic Tool For Preprocessing Imputed Genotype Dosage Data For Survival Analyses

C38 UNDERSTANDING THERAPEUTICS IN IPF: Cardiovascular Safety Of Nintedanib In Subgroups By Cardiovascular Risk At Baseline In The Tomorrow And Inpulsis Trials

P168 Safety and tolerability of nintedanib in patients with idiopathic pulmonary fibrosis (IPF): one-year data from post-marketing surveillance in the united states

Lung microbiome and disease progression in idiopathic pulmonary fibrosis: an analysis of the COMET study

Suspected acute exacerbation of idiopathic pulmonary fibrosis as an outcome measure in clinical trials

A40 CONNECTIVE TISSUE DISEASE RELATED INTERSTITIAL LUNG DISEASE: RISK FACTORS, DIAGNOSIS, AND OUTCOMES: Rheumatoid Arthritis-Associated Interstitial Lung Disease: Risk Factors For Disease Progression

A103 IPF: MORE ABOUT THERAPY AND OUTCOMES: Safety And Tolerability Of Nintedanib In Patients With Idiopathic Pulmonary Fibrosis (ipf): One-Year Data From Post-Marketing Surveillance In The United States

A42 NEW DEVELOPMENTS IN ILD RESEARCH: Regional Heterogeneity In Autoimmune Features Among Patients With Fibrotic Interstitial Lung Disease

Identification of Diagnostic Criteria for Chronic Hypersensitivity Pneumonitis: An International Modified Delphi Survey

A93 EXPLORING THE HUMAN RESPIRATORY ADAPTIVE IMMUNE RESPONSE: Ccr4-Expressing Cd4+ T Cells Are Increased In Lungs Of Patients With Idiopathic Pulmonary Fibrosis And Correlate With Lung Function

B110 NOVEL THERAPIES AND TARGETS IN FIBROSIS: Non Circulating Pulmonary Resident Memory T Cells Can Be Identified And Demonstrate Activated Phenotypes In Idiopathic Pulmonary Fibrosis

D28 THE WEB OF OMICS: DNA, RNA, AND PROTEIN MODIFICATIONS: Dna Methylation And Epigenetic Age Characterize Molecular Differences Between Idiopathic Pulmonary Fibrosis And COPD

A93 ROLE OF ADAPTIVE IMMUNITY IN LUNG DISEASE: Stratification Of Idiopathic Pulmonary Fibrosis Survival By Icos And Cd28 Surface Expression On T Cells

A75 BIG AND BIGGER (DATA): OMICS AND BIOMARKERS OF LUNG DISEASES: A Genome-Wide Network Analysis Of Gene Polymorphisms Associated With Idiopathic Pulmonary Fibrosis Susceptibility

Imatinib Treatment for Idiopathic Pulmonary Fibrosis: Randomized Placebo-controlled Trial Results

D103 DR. "NOBODY CAN DIAGNOSE INTERSTITIAL LUNG DISEASE ALONE": MULTIDISCIPLINARY EVALUATION OF INTERSTITIAL LUNG DISEASE: A Novel, Blood-Based Diagnostic Gene Signature For Rheumatoid-Arthritis Interstitial Lung Disease

A41 INTERSTITIAL LUNG DISEASE: RISK FACTORS AND OUTCOMES: Hypothyroidism In Patients With Idiopathic Pulmonary Fibrosis

C61 SURVEYING THE LANDSCAPE: OMIC APPROACHES TO STUDY LUNG DISEASE: Peripheral Blood Gene Signature Distinguishes Sarcoidosis From Idiopathic Pulmonary Fibrosis

B57 GENE REGULATION: MIRNAS AND EPIGENETICS: Micrornas Regulate The Expression Of Tollip Gene Involved In Idiopathic Pulmonary Fibrosis Susceptibility

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