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Die folgenden Publikationen sind in der Online-Universitätsbibliographie der Universität Duisburg-Essen verzeichnet. Weitere Informationen finden Sie gegebenenfalls auch auf den persönlichen Webseiten der Person.
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Diagnostik und Therapie der exogen-allergischen Alveolitis : S2k-Leitlinie der Deutschen Gesellschaft für Pneumologie und Beatmungsmedizin e. V. und der Deutschen Gesellschaft für Allergologie und klinische Immunologie e. V.In: Pneumologie Jg. 78 (2024) Nr. 12, S. 963 - 1002Online Volltext: dx.doi.org/
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Pharmacological Treatment of Idiopathic Pulmonary Fibrosis (Update) and Progressive Pulmonary Fibroses : S2k Guideline of the German Respiratory SocietyIn: Respiration: International Journal of Thoracic Medicine (2024) 540856 in pressOnline Volltext: dx.doi.org/ (Open Access)
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Serum soluble isoform of receptor for advanced glycation end product is a predictive biomarker for acute exacerbation of idiopathic pulmonary fibrosis : A German and Japanese cohort studyIn: Respiratory Research Jg. 25 (2024) Nr. 1, 405Online Volltext: dx.doi.org/ (Open Access)
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COVID-19 in patients with pulmonary alveolar proteinosis : A European multicentre studyIn: ERJ Open Research Jg. 9 (2023) Nr. 1, 00199-2022Online Volltext: dx.doi.org/ (Open Access)
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Efficacy and Safety of Pirfenidone in Advanced Versus Non-Advanced Idiopathic Pulmonary Fibrosis : Post-Hoc Analysis of Six Clinical StudiesIn: Advances in Therapy Jg. 40 (2023) Nr. 9, S. 3937 - 3955Online Volltext: dx.doi.org/ (Open Access)
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Erratum : Pharmakotherapie der idiopathischen Lungenfibrose (ein Update) und anderer progredienter pulmonaler FibrosenIn: Pneumologie Jg. 77 (2023) Nr. 2, S. e1Online Volltext: dx.doi.org/
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GLPG1205 for idiopathic pulmonary fibrosis : A phase 2 randomised placebo-controlled trialIn: European Respiratory Journal (ERJ) Jg. 61 (2023) Nr. 3, 2201794Online Volltext: dx.doi.org/ (Open Access)
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Idiopathic Pulmonary Fibrosis Is Associated with Common Genetic Variants and Limited Rare VariantsIn: American Journal of Respiratory and Critical Care Medicine (AJRCCM) Jg. 207 (2023) Nr. 9, S. 1194 - 1202Online Volltext: dx.doi.org/
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Imbalanced distribution of regulatory T cells and Th17.1 cells in the peripheral blood and BALF of sarcoidosis patients : Relationship to disease activity and the fibrotic radiographic phenotypeIn: Frontiers in Immunology Jg. 14 (2023) 1185443Online Volltext: dx.doi.org/ (Open Access)
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Pharmakotherapie der idiopathischen Lungenfibrose (ein Update) und anderer progredienter pulmonaler Fibrosen : S2k-Leitline der Deutsche Gesellschaft für Pneumologie und Beatmungsmedizin e. V.In: Pneumologie Jg. 77 (2023) Nr. 2, S. 94 - 119Online Volltext: dx.doi.org/
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S1-Leitlinie Interdisziplinäre Diagnostik interstitieller Lungenerkrankungen im ErwachsenenalterIn: Pneumologie Jg. 77 (2023) Nr. 5, S. 269 - 302Online Volltext: dx.doi.org/ (Open Access)
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Serum KL-6 as a Biomarker of Progression at Any Time in Fibrotic Interstitial Lung DiseaseIn: Journal of Clinical Medicine (JCM) Jg. 12 (2023) Nr. 3, 1173Online Volltext: dx.doi.org/ (Open Access)
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Thoracic pain in patients with chronic interstitial lung disease : an underestimated symptomIn: Frontiers in Medicine Jg. 10 (2023) 1147555Online Volltext: dx.doi.org/ Online Volltext (Open Access)
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Ziritaxestat, a Novel Autotaxin Inhibitor, and Lung Function in Idiopathic Pulmonary Fibrosis: The ISABELA 1 and 2 Randomized Clinical TrialsIn: JAMA: Journal of the American Medical Association Jg. 329 (2023) Nr. 18, S. 1567 - 1578Online Volltext: dx.doi.org/
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A New Tool to Assess Quality of Life in Patients with Idiopathic Pulmonary Fibrosis or Non-specific Interstitial PneumoniaIn: Pneumologie Jg. 76 (2022) Nr. 01, S. 25 - 34Online Volltext: dx.doi.org/ (Open Access)
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A transcriptomics-based meta-analysis identifies a cross-tissue signature for sarcoidosisIn: Frontiers in Medicine Jg. 9 (2022) 960266Online Volltext: dx.doi.org/ (Open Access)
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Comparison of a 22G Crown-Cut Needle with a Conventional 22G Needle with EBUS Guidance in Diagnosis of SarcoidosisIn: Lung Jg. 200 (2022) Nr. 5, S. 633 - 641Online Volltext: dx.doi.org/ (Open Access)
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Double Lung Transplantation for Idiopathic Pulmonary Fibrosis in a Patient with a History of Liver Transplantation and Prolonged Journey for Disease-Specific Antifibrotic TherapyIn: Case Reports in Pulmonology Jg. 2022 (2022) 4054339Online Volltext: dx.doi.org/ (Open Access)
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IL-9 and IL-9 receptor expression in lymphocytes from bronchoalveolar lavage fluid of patients with interstitial lung diseaseIn: Immunobiology Jg. 227 (2022) Nr. 5, 152258Online Volltext: dx.doi.org/
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Nanotechnology-facilitated vaccine development during the coronavirus disease 2019 (COVID-19) pandemicIn: Exploration Jg. 2 (2022) Nr. 5, 20210082Online Volltext: dx.doi.org/ (Open Access)
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Safety and tolerability of nintedanib in patients with progressive fibrosing interstitial lung diseases : Data from the randomized controlled INBUILD trialIn: Respiratory Research Jg. 23 (2022) Nr. 1, 85Online Volltext: dx.doi.org/ (Open Access)
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Transbronchial cryobiopsy : the right procedure for the right patient in the right place at the right timeIn: European Respiratory Journal (ERJ) Jg. 60 (2022) Nr. 5, 2201648Online Volltext: dx.doi.org/
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Bronchoalveolar lavage and lung biopsy in connective tissue diseases, to do or not to do?In: Therapeutic Advances in Musculoskeletal Disease Jg. 13 (2021) S. 1 - 21Online Volltext: dx.doi.org/ (Open Access)
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Bronchoscopic performance of bronchoalveolar lavage in Germany - A call for standardizationIn: Sarcoidosis Vasculitis and Diffuse Lung Diseases Jg. 38 (2021) Nr. 1,Online Volltext: dx.doi.org/
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Immunohistochemical Detection of Potential Microbial Antigens in Granulomas in the Diagnosis of SarcoidosisIn: Journal of Clinical Medicine (JCM) Jg. 10 (2021) Nr. 5, 983Online Volltext: dx.doi.org/ Online Volltext (Open Access)
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Misconceptions regarding symptoms of sarcoidosisIn: The Lancet Respiratory Medicine Jg. 9 (2021) Nr. 8, S. 816 - 818Online Volltext: dx.doi.org/
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Phase 2 trial to assess lebrikizumab in patients with idiopathic pulmonary fibrosisIn: European Respiratory Journal (ERJ) Jg. 57 (2021) Nr. 2, S. 1902442Online Volltext: dx.doi.org/ Online Volltext (Open Access)
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Pirfenidone in patients with progressive fibrotic interstitial lung diseases other than idiopathic pulmonary fibrosis (RELIEF) : A double-blind, randomised, placebo-controlled, phase 2b trialIn: The Lancet Respiratory Medicine Jg. 9 (2021) Nr. 5, S. 476 - 486Online Volltext: dx.doi.org/ Online Volltext (Open Access)
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Potential clinical utility of MUC5B und TOLLIP single nucleotide polymorphisms (SNPs) in the management of patients with IPFIn: Orphanet Journal of Rare Diseases Jg. 16 (2021) Nr. 1, 111Online Volltext: dx.doi.org/ Online Volltext (Open Access)
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S2K Guideline for Diagnosis of Idiopathic Pulmonary FibrosisIn: Respiration: International Journal of Thoracic Medicine Jg. 100 (2021) Nr. 3, S. 238 - 271Online Volltext: dx.doi.org/ (Open Access)
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Sprachliche Validierung des Fibrose-Fragebogens zur Erfassung der Lebensqualität bei Patienten mit idiopathischer Lungenfibrose und idiopathischer nichtspezifischer interstitieller PneumonieIn: Pneumologie Jg. 75 (2021) Nr. 10, S. 753 - 760Online Volltext: dx.doi.org/
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Suggestions for improving clinical utility of future guidelines for diagnosis and management of idiopathic pulmonary fibrosis : results of a Delphi surveyIn: European Respiratory Journal (ERJ) Jg. 57 (2021) Nr. 4, S. 2004219Online Volltext: dx.doi.org/ Online Volltext (Open Access)
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The Role of Diverse Immune Cells in SarcoidosisIn: Frontiers in Immunology Jg. 12 (2021) 788502Online Volltext: dx.doi.org/ (Open Access)
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The diagnosis and treatment of pulmonary fibrosisIn: Deutsches Ärzteblatt international Jg. 118 (2021) Nr. 9, S. 152 - 162Online Volltext: dx.doi.org/ (Open Access)
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A Comparison of Existing Questionnaires for Identifying the Causes of Interstitial and Rare Lung DiseasesIn: Respiration: International Journal of Thoracic Medicine Jg. 99 (2020) Nr. 2, S. 119 - 124Online Volltext: dx.doi.org/
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Azathioprine for Connective Tissue Disease-Associated Interstitial Lung DiseaseIn: Respiration: International Journal of Thoracic Medicine Jg. 99 (2020) Nr. 8, S. 628 - 636Online Volltext: dx.doi.org/
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Delphi consensus recommendations for a treatment algorithm in pulmonary sarcoidosisIn: European Respiratory Review (ERR) Jg. 29 (2020) Nr. 155, 190146Online Volltext: dx.doi.org/ (Open Access)
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Hypersensitivity pneumonitisIn: Nature Reviews Disease Primers Jg. 6 (2020) Nr. 1, S. 65Online Volltext: dx.doi.org/
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Nachruf Prof. Dr. Dr. Claus KroegelIn: Pneumologie Jg. 74 (2020) Nr. 10, S. 695 - 696Online Volltext: dx.doi.org/
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Pamrevlumab, an anti-connective tissue growth factor therapy, for idiopathic pulmonary fibrosis (PRAISE) : A phase 2, randomised, double-blind, placebo-controlled trialIn: The Lancet Respiratory Medicine Jg. 8 (2020) Nr. 1, S. 25 - 33Online Volltext: dx.doi.org/
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Progressive fibrosing interstitial lung disease : clinical uncertainties, consensus recommendations, and research prioritiesIn: The Lancet Respiratory Medicine Jg. 8 (2020) Nr. 9, S. 925 - 934Online Volltext: dx.doi.org/ (Open Access)
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S2K-Leitlinie zur Diagnostik der idiopathischen LungenfibroseIn: Pneumologie Jg. 74 (2020) Nr. 5, S. 263 - 293Online Volltext: dx.doi.org/
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Safety and tolerability of nintedanib in patients with systemic sclerosis-associated interstitial lung disease : Data from the SENSCIS trialIn: Annals of the Rheumatic Diseases (ARD) Jg. 79 (2020) Nr. 11, S. 1478 - 1484Online Volltext: dx.doi.org/ (Open Access)
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Transbronchial cryobiopsy increases diagnostic confidence in interstitial lung disease: A prospective multicentre trialIn: European Respiratory Journal (ERJ) Jg. 56 (2020) Nr. 6, S. 1901520Online Volltext: dx.doi.org/ (Open Access)
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Baseline High-Resolution CT Findings Predict Acute Exacerbation of Idiopathic Pulmonary Fibrosis : German and Japanese Cohort StudyIn: Journal of Clinical Medicine (JCM) Jg. 8 (2019) Nr. 12, 2069Online Volltext: dx.doi.org/ (Open Access)
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Changes in serum KL-6 levels are associated with the development of chronic lung allograft dysfunction in lung transplant recipientsIn: Transplant Immunology Jg. 52 (2019) S. 40 - 44Online Volltext: dx.doi.org/
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Correction to: The burden of sarcoidosis symptoms from a patient perspectiveIn: Lung Jg. 197 (2019) Nr. 2, S. 163Online Volltext: dx.doi.org/ (Open Access)
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Diagnostic value of BAL lymphocytosis in patients with indeterminate for usual interstitial pneumonia imaging patternIn: European Respiratory Journal (ERJ) Jg. 54 (2019) Nr. 5, Article-No: 1901144Online Volltext: dx.doi.org/ (Open Access)
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Die Rolle der Luftschadstoffe für die Gesundheit : Eine Replik auf die Expertise der Internationalen Gesellschaft für Umweltepidemiologie (ISEE) und der European Respiratory Society (ERS)In: Pneumologie Jg. 73 (2019) Nr. 5, S. 274 - 287Online Volltext: dx.doi.org/ (Open Access)
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Effect of pirfenidone in patients with more advanced idiopathic pulmonary fibrosisIn: Respiratory Research Jg. 20 (2019) Nr. 1, S. 55Online Volltext: dx.doi.org/ (Open Access)
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Efficacy of Pirfenidone in the Context of Multiple Disease Progression Events in Patients With Idiopathic Pulmonary FibrosisIn: Chest Jg. 155 (2019) Nr. 4, S. 712 - 719Online Volltext: dx.doi.org/ (Open Access)
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Erratum zu: Differenzialdiagnose interstitieller Lungenerkrankungen – „Interstitial pneumonia with autoimmune features“ (IPAF)In: Der Pneumologe Jg. 16 (2019) Nr. 1, S. 39Online Volltext: dx.doi.org/ (Open Access)
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Idiopathic interstitial pneumonia or idiopathic interstitial pneumonitis: what's in a name?In: European Respiratory Journal (ERJ) Jg. 53 (2019) Nr. 2, S. 1800994Online Volltext: dx.doi.org/ (Open Access)
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Long-term safety and tolerability of nintedanib in patients with idiopathic pulmonary fibrosis : results from the open-label extension study, INPULSIS-ONIn: The Lancet Respiratory Medicine Jg. 7 (2019) Nr. 1, S. 60 - 68Online Volltext: dx.doi.org/
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Pirfenidone in patients with idiopathic pulmonary fibrosis and more advanced lung function impairmentIn: Respiratory Medicine Jg. 153 (2019) S. 44 - 51Online Volltext: dx.doi.org/ (Open Access)
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Quantitative lipidomics in pulmonary alveolar proteinosisIn: American Journal of Respiratory and Critical Care Medicine (AJRCCM) Jg. 200 (2019) Nr. 7, S. 881 - 887Online Volltext: dx.doi.org/
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The Burden of Sarcoidosis Symptoms from a Patient PerspectiveIn: Lung Jg. 197 (2019) Nr. 2, S. 155 - 161Online Volltext: dx.doi.org/ (Open Access)
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Utility of Anti-DSF70 Antibodies to Predict Connective Tissue Disease in Patients Originally Presenting with Idiopathic Interstitial PneumoniaIn: Respiration: International Journal of Thoracic Medicine Jg. 98 (2019) Nr. 1, S. 29 - 37Online Volltext: dx.doi.org/ Online Volltext (Open Access)
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An emerging frontier in the treatment of acute exacerbation of idiopathic pulmonary fibrosisIn: Respiratory Investigation Jg. 56 (2018) Nr. 2, S. 97 - 99Online Volltext: dx.doi.org/
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Anti-Interleukin-5-Therapie und eosinophile Granulomatose mit Polyangiitis : Ein Aufbruch?In: Der Pneumologe Jg. 15 (2018) Nr. 3, S. 189 - 192Online Volltext: dx.doi.org/
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Anti-acid therapy in idiopathic pulmonary fibrosis : insights from the INPULSIS® trialsIn: Respiratory Research Jg. 19 (2018) S. 167Online Volltext: dx.doi.org/ (Open Access)
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Differenzialdiagnose interstitieller LungenerkrankungenIn: Der Pneumologe Jg. 15 (2018) Nr. 6, S. 413 - 418Online Volltext: dx.doi.org/
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Effect of pirfenidone on exercise capacity and dyspnea in patients with idiopathic pulmonary fibrosis (IPF) and more advanced lung function impairmentIn: Chest Jg. 154 (2018) Nr. Suppl. 4, S. 432A - 433AOnline Volltext: dx.doi.org/
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Eosinophile Granulomatose und Polyangiitis : Diagnostik und TherapieIn: Der Pneumologe Jg. 15 (2018) Nr. 5, S. 333 - 343Online Volltext: dx.doi.org/
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Eosinophile Granulozyten : physiologische und pathophysiologische FunktionenIn: Der Pneumologe Jg. 15 (2018) Nr. 5, S. 299 - 308Online Volltext: dx.doi.org/
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Gastroesophageal Reflux Disease in Idiopathic Pulmonary Fibrosis : Uncertainties and ControversiesIn: Respiration: International Journal of Thoracic Medicine Jg. 96 (2018) Nr. 6, S. 571 - 587Online Volltext: dx.doi.org/
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German Guideline for Idiopathic Pulmonary Fibrosis : Update on Pharmacological Therapies 2017In: Pneumologie Jg. 72 (2018) Nr. 2, S. 155 - 168Online Volltext: dx.doi.org/ (Open Access)
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Long-term treatment of patients with idiopathic pulmonary fibrosis with nintedanib : results from the TOMORROW trial and its open-label extensionIn: Thorax Jg. 73 (2018) Nr. 6, S. 581 - 583Online Volltext: dx.doi.org/ (Open Access)
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Modified GAP stage as a predictor of acute exacerbation in idiopathic pulmonary fibrosisIn: European Respiratory Journal (ERJ) Jg. 52 (2018) Nr. Suppl. 62, S. PA2907Online Volltext: dx.doi.org/
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Nailfold capillaroscopy findings in ILD patients : results from a single centre investigationIn: European Respiratory Journal (ERJ) Jg. 52 (2018) Nr. Suppl. 62, S. PA2951Online Volltext: dx.doi.org/
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Patientenfragebogen zur Erfassung der Ursachen interstitieller und seltener Lungenerkrankungen - klinische Sektion der DGPIn: Pneumologie Jg. 72 (2018) Nr. 6, S. 446 - 457Online Volltext: dx.doi.org/
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Patterns of discontinuation in patients with IPF treated with open-label nintedanib : data from INPULSIS-ONIn: European Respiratory Journal (ERJ) Jg. 52 (2018) Nr. Suppl. 62, S. PA4777Online Volltext: dx.doi.org/ Online Volltext (Open Access)
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Phenotypes of organ involvement in sarcoidosisIn: European Respiratory Journal (ERJ) Jg. 51 (2018) Nr. 1, S. 1700991Online Volltext: dx.doi.org/ (Open Access)
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Serum YKL-40 in workers at an indium-tin oxide production facility - ReplyIn: Respirology Jg. 23 (2018) Nr. 3, S. 342Online Volltext: dx.doi.org/ (Open Access)
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Statin Therapy and Outcomes in Trials of Nintedanib in Idiopathic Pulmonary FibrosisIn: Respiration: International Journal of Thoracic Medicine Jg. 95 (2018) Nr. 5, S. 317 - 326Online Volltext: dx.doi.org/ (Open Access)
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The European IPF Registry : Addressing challenges and characteristics of patients with Idiopathic Pulmonary FibrosisIn: European Respiratory Journal (ERJ) Jg. 52 (2018) Nr. Suppl. 62, S. PA2198Online Volltext: dx.doi.org/
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The European IPF registry (eurIPFreg) : baseline characteristics and survival of patients with idiopathic pulmonary fibrosisIn: Respiratory Research Jg. 19 (2018) S. 141Online Volltext: dx.doi.org/ (Open Access)
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An Open-Label Study of the Long-Term Safety of Pirfenidone in Patients with Idiopathic Pulmonary Fibrosis (RECAP)In: Respiration: International Journal of Thoracic Medicine Jg. 94 (2017) Nr. 5, S. 408 - 415Online Volltext: dx.doi.org/ (Open Access)
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Annual rate of FVC decline in Patients with IPF treared with Pirfenidone : Pooled Analysis (Encore)In: Respirology Jg. 22 (2017) Nr. Suppl. 2, S. 79Online Volltext: dx.doi.org/ Online Volltext (Open Access)
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Antacid Therapy and Disease Progression in Patients with Idiopathic Pulmonary Fibrosis Who Received PirfenidoneIn: Respiration: International Journal of Thoracic Medicine Jg. 93 (2017) Nr. 6, S. 415 - 423Online Volltext: dx.doi.org/ (Open Access)
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Differential diagnosis of granulomatous lung disease : Clues and pitfallsIn: European Respiratory Review (ERR) Jg. 26 (2017) Nr. 145, 170012Online Volltext: dx.doi.org/ (Open Access)
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Effect of continued Pirfenidone treatment following >= 15% decline in 6MWD in IPF Patients-Pooled Analysis (Encore)In: Respirology Jg. 22 (2017) Nr. Suppl. 2, S. 79Online Volltext: dx.doi.org/ Online Volltext (Open Access)
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Effect of pirfenidone on mortality : pooled analyses and meta-analyses of clinical trials in idiopathic pulmonary fibrosisIn: The Lancet Respiratory Medicine Jg. 5 (2017) Nr. 1, S. 33 - 41Online Volltext: dx.doi.org/
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Effect of statins on disease-related outcomes in patients with idiopathic pulmonary fibrosisIn: Thorax Jg. 72 (2017) Nr. 2, S. 148 - 153Online Volltext: dx.doi.org/ (Open Access)
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Eosinophile Granulomatose und Polyangiitis (Churg-Strauss-Syndrom) : Pathogenetische und klinische Grundlagen, Diagnostik und BehandlungszugāngeIn: Arzneimitteltherapie (AMT) Jg. 35 (2017) Nr. 11, S. 413 - 426
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Epidemiologie und klinisches Erscheinungsbild der SarkoidoseIn: Klinische Monatsblätter für Augenheilkunde Jg. 234 (2017) Nr. 6, S. 790 - 795Online Volltext: dx.doi.org/
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Erfahrungen und unterstützende Hinweise zur Anwendung von Nintedanib bei Patienten mit idiopathischer LungenfibroseIn: Pneumologie Jg. 71 (2017) Nr. 9, S. 567 - 579Online Volltext: dx.doi.org/
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FAM13A polymorphism as a prognostic factor in patients with idiopathic pulmonary fibrosisIn: Respiratory Medicine Jg. 123 (2017) S. 105 - 109Online Volltext: dx.doi.org/
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Helicobacter Pylori As A Risk Factor For Acute Exacerbation In Idiopathic Pulmonary FibrosisIn: American Journal of Respiratory and Critical Care Medicine (AJRCCM) Jg. 195 (2017) S. A3468
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Idiopathic pleuroparenchymal fibroelastosis (PPFE) : A case study of a rare entityIn: Revista Portuguesa de Pneumologia (English Edition) Jg. 23 (2017) Nr. 6, S. 352 - 355Online Volltext: dx.doi.org/ (Open Access)
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M32 Effect of pirfenidone on all-cause mortality (acm) and forced vital capacity (fvc) in idiopathic pulmonary fibrosis (ipf) patients with low fvc and/or low dlco : analysis of pooled data from ascend and capacityIn: Thorax Jg. 72 (2017) Nr. Suppl. 3, A254Online Volltext: dx.doi.org/
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Pirfenidone safety and adverse event management in idiopathic pulmonary fibrosisIn: European Respiratory Review (ERR) Jg. 26 (2017) Nr. 146, 170057Online Volltext: dx.doi.org/ (Open Access)
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Potential Utility Of Anti Dfs70 Antibodies To Exclude Systemic Autoimmune Rheumatic Disease (sard) In Patients With Interstitial Lung Disease (ild)In: American Journal of Respiratory and Critical Care Medicine (AJRCCM) Jg. 195 (2017) S. A7129
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Quartile Forced Vital Capacity Changes At 3, 6, 9, And 12 Months With Pirfenidone In Patients With Idiopathic Pulmonary Fibrosis : A Pooled Phase Iii AnalysisIn: American Journal of Respiratory and Critical Care Medicine (AJRCCM) Jg. 195 (2017) S. A5395
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Reply : Effect of Nintedanib in Patients with Idiopathic Pulmonary FibrosisIn: American Journal of Respiratory and Critical Care Medicine (AJRCCM) Jg. 195 (2017) Nr. 9, S. 1275Online Volltext: dx.doi.org/
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Reply [Effect of Nintedanib in Patients with Idiopathic Pulmonary Fibrosis ]In: American Journal of Respiratory and Critical Care Medicine (AJRCCM) Jg. 195 (2017) Nr. 9, S. 1275Online Volltext: dx.doi.org/
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S2k-Leitlinie Idiopathische Lungenfibrose – Update zur medikamentösen Therapie 2017In: Pneumologie Jg. 71 (2017) Nr. 7, S. 460 - U140Online Volltext: dx.doi.org/
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Serum YKL-40 as predictor of outcome in hypersensitivity pneumonitisIn: European Respiratory Journal (ERJ) Jg. 49 (2017) Nr. 2,Online Volltext: dx.doi.org/
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Serum YKL-40 is a reliable biomarker for pulmonary alveolar proteinosisIn: Respirology Jg. 22 (2017) Nr. 7, S. 1371 - 1378Online Volltext: dx.doi.org/
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Transbronchial Lung Cryobiopsy in Diffuse Parenchymal Lung Disease : Comparison between Biopsy from 1 Segment and Biopsy from 2 Segments-Diagnostic Yield and ComplicationsIn: Respiration: International Journal of Thoracic Medicine Jg. 93 (2017) Nr. 4, S. 285 - 292Online Volltext: dx.doi.org/ (Open Access)
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A Global Survey on Whole Lung Lavage in Pulmonary Alveolar ProteinosisIn: Chest Jg. 150 (2016) Nr. 1, S. 251 - 253Online Volltext: dx.doi.org/
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A confusing case report of pulmonary langerhans cell histiocytosis and literature reviewIn: Open Medicine Jg. 11 (2016) Nr. 1, S. 178 - 182Online Volltext: dx.doi.org/ (Open Access)
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An Important Step Forward, but Still a Way to GoIn: American Journal of Respiratory and Critical Care Medicine (AJRCCM) Jg. 193 (2016) Nr. 3, S. 340 - 341
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Analysis of Patients With Idiopathic Pulmonary Fibrosis (IPF) With More Severe Lung Function Impairment Treated With Pirfenidone in RecapIn: Chest Jg. 150 (2016) Nr. 4 Suppl., S. 537AOnline Volltext: dx.doi.org/
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Antacid therapy and disease outcomes in idiopathic pulmonary fibrosis : a pooled analysisIn: The Lancet Respiratory Medicine Jg. 4 (2016) Nr. 5, S. 381 - 389Online Volltext: dx.doi.org/ (Open Access)
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Anti-acid treatment in patients with IPF : interpret results from post-hoc, subgroup, and exploratory analyses with great caution – Authors' replyIn: The Lancet Respiratory Medicine Jg. 4 (2016) Nr. 9, S. e48Online Volltext: dx.doi.org/
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Bronchoscopic Lung Cryobiopsy Increases Diagnostic Confidence in the Multidisciplinary Diagnosis of Idiopathic Pulmonary FibrosisIn: American Journal of Respiratory and Critical Care Medicine (AJRCCM) Jg. 193 (2016) Nr. 7, S. 745 - 752Online Volltext: dx.doi.org/
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Clinical Manifestations of Respiratory Bronchiolitis as an Incidental Finding in Surgical Lung Biopsies : A Retrospective Analysis of a Large Austrian RegistryIn: Respiration: International Journal of Thoracic Medicine Jg. 91 (2016) Nr. 1, S. 26 - 33Online Volltext: dx.doi.org/
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Clinical Spectrum Time Course in Non Anti Jo-1 Positive Antisynthetase SyndromeIn: Annals of the Rheumatic Diseases (ARD) Jg. 75 (2016) Nr. Suppl. 2, S. 540 - 541Online Volltext: dx.doi.org/
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Deutschsprachige Validierung des „Kingʼs Brief Interstitial Lung Disease (K-BILD)“ Lebensqualitätsfragebogens für interstitielle LungenerkrankungenIn: Pneumologie Jg. 70 (2016) Nr. 11, S. 742 - 746Online Volltext: dx.doi.org/
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Effect Of Continued Treatment With Pirfenidone Following A >= 10% Relative Decline In Percent Predicted Forced Vital Capacity In Patients With Idiopathic Pulmonary Fibrosis (ipf)In: American Journal of Respiratory and Critical Care Medicine (AJRCCM) Jg. 193 (2016) S. A4995
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Effect of continued treatment with pirfenidone following clinically meaningful declines in forced vital capacity : analysis of data from three phase 3 trials in patients with idiopathic pulmonary fibrosisIn: Thorax Jg. 71 (2016) Nr. 5, S. 429 - 435Online Volltext: dx.doi.org/
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Efficacy of pirfenidone in patients with idiopathic pulmonary fibrosis with more preserved lung functionIn: European Respiratory Journal (ERJ) Jg. 48 (2016) Nr. 3, S. 843 - 851Online Volltext: dx.doi.org/
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Erratum: 58-year old woman with primary biliary cirrhosis and crepitationsIn: Deutsche Medizinische Wochenschrift - DMW Jg. 141 (2016) Nr. 4, S. 241Online Volltext: dx.doi.org/
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Fam13a Polymorphism As A Prognostic Factor In Patients With Idiopathic Pulmonary FibrosisIn: American Journal of Respiratory and Critical Care Medicine (AJRCCM) Jg. 193 (2016) S. A4982
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How to handle IPF – the new Portuguese consensus documentIn: Revista Portuguesa de Pneumologia (English Edition) Jg. 22 (2016) Nr. 2, S. 70 - 72Online Volltext: dx.doi.org/ (Open Access)
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Interstitial pneumonia with autoimmune features : a critical appraisal of the new definitionIn: Current Opinion in Pulmonary Medicine Jg. 22 (2016) Nr. 5, S. 442 - 449Online Volltext: dx.doi.org/
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Long-term safety of pirfenidone in patients with idiopathic pulmonary fibrosis : pooled analysis of 4 clinical trialsIn: Thorax Jg. 71 (2016) Nr. Suppl. 3, S. A175 - A176Online Volltext: dx.doi.org/
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MFAP4 : A candidate biomarker for hepatic and pulmonary fibrosis?In: Sarcoidosis Vasculitis and Diffuse Lung Diseases Jg. 33 (2016) Nr. 1, S. 41 - 50
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MUC1 gene polymorphisms are associated with serum KL-6 levels and pulmonary dysfunction in pulmonary alveolar proteinosisIn: Orphanet Journal of Rare Diseases Jg. 11 (2016) S. 48Online Volltext: dx.doi.org/ (Open Access)
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(100) - KL-6 Changes in Serum Can Be Predictive of Chronic Lung Allograft Dysfunction in Lung Transplant RecipientsIn: The Journal of Heart and Lung Transplantation Jg. 34 (2015) Nr. 4 Suppl., S. 46Online Volltext: dx.doi.org/
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CC-chemokine ligand 2 inhibition in idiopathic pulmonary fibrosis : a phase 2 trial of carlumabIn: European Respiratory Journal (ERJ) Jg. 46 (2015) Nr. 6, S. 1740 - 1750Online Volltext: dx.doi.org/ (Open Access)
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6-Minute walk distance is an independent predictor of mortality in patients with idiopathic pulmonary fibrosisIn: European Respiratory Journal (ERJ) Jg. 43 (2014) Nr. 5, S. 1421 - 1429Online Volltext: dx.doi.org/
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Triple therapy in idiopathic pulmonary fibrosis : an alarming press releaseIn: European Respiratory Journal (ERJ) Jg. 39 (2012) Nr. 4, S. 805 - 806Online Volltext: dx.doi.org/
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Pulmonary alveolar proteinosis associated with dust inhalation : Not secondary but autoimmune?In: American Journal of Respiratory and Critical Care Medicine Jg. 181 (2010) Nr. 5, S. 427 - 428Online Volltext: dx.doi.org/
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Prognostic relevance of autoantibodies in patients with hypersensitivity pneumonitis (HP) : A German multicentre study
European-Respiratory-Society Congress (ERS); SEP 07-11, 2024; Vienna, Austria,In: European Respiratory Journal (ERJ) Jg. 64 (2024) Nr. Suppl. 68, PA2453Online Volltext: dx.doi.org/ -
Die Etablierung einer durchflusszytometrischen Multiparameter-Analyse der BAL und ihre Validierung durch Korrelation mit den Befunden der lichtmikroskopischen Routinediagnostik
63. Kongress der Deutschen Gesellschaft für Pneumologie und Beatmungsmedizin e. V.,In: Pneumologie Jg. 77 (2023) Nr. S 01, S. S85 - S86Online Volltext: dx.doi.org/ -
Progrediente Pulmonale Fibrose (PPF) bei Patienten mit exogen allergischer Alveolitis
63. Kongress der Deutschen Gesellschaft für Pneumologie und Beatmungsmedizin e. V.,In: Pneumologie Jg. 77 (2023) Nr. S 01, S. S102Online Volltext: dx.doi.org/ -
COVID-19 in patients with Pulmonary Alveolar Proteinosis : A European multicenter study
ERS International Congress 2022 ; 4-6 September 2022, Barcelona, Spain and online,In: European Respiratory Journal (ERJ) Jg. 60 (2022) Nr. Supplement 66,Online Volltext: dx.doi.org/ -
Comparison of a new Punch Needle with a conventional 22-gauge Needle in EBUS-TBNA in Patients with suspected Sarcoidosis
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Comparison of a 22G crown-cut needle with a conventional 22G needle with EBUS guidance in diagnosis of sarcoidosisIn: European Respiratory Journal (ERJ) Jg. 58 (2021) Nr. Suppl. 65, PA2454Online Volltext: dx.doi.org/
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Histological confidence of transbronchial cryobiopsy in interstitial lung diseases is influenced by sample sizeIn: European Respiratory Journal (ERJ) Jg. 58 (2021) Nr. Suppl. 65, OA233Online Volltext: dx.doi.org/
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Prevalence and quantification of thoracic pain (TP) through quantitative sensory testing (QST) in patients with chronic interstitial lung disease (cILD)In: European Respiratory Journal (ERJ) Jg. 58 (2021) Nr. Suppl. 65, PA2343Online Volltext: dx.doi.org/
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Results of a phase 2 study of GLPG1205 for idiopathic pulmonary fibrosis (PINTA)In: European Respiratory Journal (ERJ) Jg. 58 (2021) Nr. Suppl. 65, RCT2904Online Volltext: dx.doi.org/
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Association between weight loss and decline in FVC in patients with IPF
61. Kongress der Deutschen Gesellschaft für Pneumologie und Beatmungsmedizin e.V.; 25.–28.03.2020 (verschoben auf 2021); Leipzig,In: Pneumologie Jg. 74 (2020) Nr. Suppl. 1, S. S100 - S101Online Volltext: dx.doi.org/ -
Cytokines, chemokines and growth factors concentration in BAL fluid from patients with Idiopathic pulmonary fibrosis (IPF) and nonspecific interstitial pneumonia (NSIP)
ERS Virtual Congress 2020,In: European Respiratory Journal (ERJ) Jg. 56 (2020) Nr. Suppl. 64,Online Volltext: dx.doi.org/ -
Cytokines, chemokines and growth factors concentration in BAL fluid from patients with idiopathic pulmonary fibrosis (IPF) and nonspecific interstitial pneumonia (NSIP)
61. Kongress der Deutschen Gesellschaft für Pneumologie und Beatmungsmedizin e.V.; 25.–28.03.2020 (verschoben auf 2021); Leipzig,In: Pneumologie Jg. 74 (2020) Nr. Suppl. 1, S. S90 - S91Online Volltext: dx.doi.org/ -
Disease Progression Events in Trials of Nintedanib in Patients with Idiopathic Pulmonary FibrosisIn: American Journal of Respiratory and Critical Care Medicine (AJRCCM) Jg. 201 (2020) S. A4548Online Volltext: dx.doi.org/
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Klinische Nutzbarkeit eines mit Serum KL-6 modifizierten GAP-Indexes bei Patienten mit interstitiellen Lungenerkrankungen (ILD)
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Nintedanib dose adjustments and adverse events in patients with progressive autoimmune disease-related interstitial lung diseases in the inbuild trialIn: Annals of the Rheumatic Diseases (ARD) Jg. 79 (2020) Nr. Suppl. 1, S. 1015Online Volltext: dx.doi.org/ (Open Access)
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Potential Clinical Utility of Serum KL-6 for Improving the GAP-Staging in Patients with Interstitial Lung Diseases (ILD)
ATS 2020 International Conference, 15.-20. Mai 2020, Philadelphia, USA - abgesagt,In: American Journal of Respiratory and Critical Care Medicine (AJRCCM) Jg. 201 (2020) S. A4037Online Volltext: dx.doi.org/ -
Safety and Tolerability of Nintedanib in Patients with Fibrosing ILDs : a Comparison of the INBUILD and INPULSIS Trials
ATS 2020 International Conference, 15.-20. Mai 2020, Philadelphia, USA - abgesagt,In: American Journal of Respiratory and Critical Care Medicine (AJRCCM) Jg. 201 (2020) S. A1506Online Volltext: dx.doi.org/ -
The Gender-Age-Physiology (GAP) Index enhanced with KL-6 serum level for predicting disease progression in interstitial lung diseases (ILD)
ERS International Congress 2020,In: European Respiratory Journal (ERJ) Jg. 56 (2020) Nr. Suppl. 64,Online Volltext: dx.doi.org/ -
A comparison of existing questionnaires for identifying the causes of interstitial and rare lung diseasesIn: European Respiratory Journal (ERJ) Jg. 54 (2019) Nr. Suppl. 63, S. PA4728Online Volltext: dx.doi.org/
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Potential Clinical Utility of MUC5B and TOLLIP Single Nucleotide Polymorphisms (SNP) in the Management of Patients with IPF : Preliminary Results
Herbsttagung der Sektion Zellbiologie in der Deutschen Gesellschaft für Pneumologie und Beatmungsmedizin e. V., Essen, 09.–10.11.2018,In: Pneumologie Jg. 73 (2019) Nr. 02, S. 113Online Volltext: dx.doi.org/ -
Potential clinical utility of MUC5B and TOLLIP single nucleotide polymorphisms (SNP) in in the management of patients with IPFIn: European Respiratory Journal (ERJ) Jg. 54 (2019) Nr. Suppl. 63, S. PA5370Online Volltext: dx.doi.org/
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Safety and pharmacokinetics of nintedanib plus sildenafil in the INSTAGE trialIn: European Respiratory Journal (ERJ) Jg. 54 (2019) Nr. Suppl. 63, S. PA1354Online Volltext: dx.doi.org/
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Serum KL-6 as a biomarker for interstitial lung diseases in a clinical setting: application of a fully automated immunoassayIn: European Respiratory Journal (ERJ) Jg. 54 (2019) Nr. Suppl. 63, S. PA4697Online Volltext: dx.doi.org/
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Clinical Relevance of Antinuclear Antibodies (ANA) in Patients with Hypersensitivity Pneumonitis (HP) : A Single Centre Experience
International Conference of the American Thoracic Society 2018 ; ATS 2018 ; May 18-23, 2018. San Diego,In: American Journal of Respiratory and Critical Care Medicine (AJRCCM) Jg. 197 (2018) Nr. 9, abstract issue, S. A3019 -
Multiple progression events in patients with idiopathic pulmonary fibrosis (IPF)
Annual Scientific Meeting of the Australia & New Zealand Society of Respiratory Science and The Thoracic Society of Australia and New Zealand (ANZSRS/TSANZ) ; 23–27 March 2018, Adelaide,In: Respirology Jg. 23 (2018) Nr. Suppl. 1, S. 102Online Volltext: dx.doi.org/ (Open Access) -
The RIFF Study (Cohort B) : A Phase II, Randomized, Double-Blind, Placebo-Controlled Trial of Lebrikizumab in Combination with Pirfenidone in Patients with Idiopathic Pulmonary Fibrosis
International Conference of the American Thoracic Society 2018 ; ATS 2018 ; May 18-23, 2018, San Diego,In: American Journal of Respiratory and Critical Care Medicine (AJRCCM) Jg. 197 (2018) Nr. 9, abstract issue, S. A6168 -
BAL findings in interstitial lung diseaseIn: Bronchoalveolar Lavage in Basic Research and Clinical Medicine / Schildgen, Oliver; Schildgen, Verena; Brockmann, Michael (Hrsg.) 2023, S. 66 - 93Online Volltext: dx.doi.org/
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Definition and history of sarcoidosisIn: Sarcoidosis / Bonella, Francesco; Culver, Daniel A.; Israël-Biet, Dominique (Hrsg.) 2022, S. 1 - 7Online Volltext: dx.doi.org/
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Idiopathic pulmonary fibrosisIn: ERS Monograph Lausanne Jg. 71 (2016) XI, 274 Seiten, Ill.
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Progressive pulmonary fibrosis in patients with chronic hypersensitivity pneumonitis (cHP) : a single center experience
International Congress of the European Respiratory Society (ERS) 2023 ; 9 - 13 September 2023, Milan, Italy,In: European Respiratory Journal (ERJ) Jg. 62 (2023) Nr. Supplement 67: ERS International Congress 2023 abstracts, PA2883Online Volltext: dx.doi.org/