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Longitudinal clinical outcomes in a real-world population of patients with idiopathic pulmonary fibrosis: the PROOF registry

Respiratory research, 2019-10, Vol.20 (1), p.231-231, Article 231

2019

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Treatment failure and hospital readmissions in severe COPD exacerbations treated with azithromycin versus placebo - a post-hoc analysis of the BACE randomized controlled trial

Respiratory research, 2019-10, Vol.20 (1), p.237-12, Article 237

2019

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Diagnostic Ability of a Dynamic Multidisciplinary Discussion in Interstitial Lung Diseases

Chest, 2018-06, Vol.153 (6), p.1416-1423

2018

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Should oral anticoagulation be discontinued after 3 months in the setting of a first high-risk pulmonary embolism secondary to a major transient/reversible risk factor?

The European respiratory journal, 2020-01, Vol.55 (1), p.1902028

2020

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Azithromycin for prevention of exacerbations in severe asthma (AZISAST): a multicentre randomised double-blind placebo-controlled trial

Thorax, 2013-04, Vol.68 (4), p.322-329

2013

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COVID-19–Associated Eosinopenia in a Patient With Chronic Eosinophilia Due to Chronic Strongyloidiasis

Infectious diseases in clinical practice (Baltimore, Md.), 2021-09, Vol.29 (5), p.e305-e306

2021

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Diagnostic Ability of a Dynamic Multidisciplinary Discussion in Interstitial Lung Diseases: A Retrospective Observational Study of 938 Cases

Chest, 2018-06, Vol.153 (6), p.1416-1423

2018

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Correlation of BAL Cell Count and Pulmonary Function Tests in the Era of Antifibrotics: Data From the Belgium-Luxembourg Idiopathic Pulmonary Fibrosis Registry

Chest, 2023-02, Vol.163 (2), p.358-361

2023

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Correlation of BAL Cell Count and Pulmonary Function Tests in the Era of Antifibrotics

Chest, 2023-02, Vol.163 (2), p.358-361

2023

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Effect of anti-interleukin drugs in patients with COVID-19 and signs of cytokine release syndrome (COV-AID): a factorial, randomised, controlled trial

The lancet respiratory medicine, 2021-12, Vol.9 (12), p.1427-1438

2021

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Clinical course of suspected familial and sporadic idiopathic pulmonary fibrosis: Data from the PROOF‐Next registry

Respirology (Carlton, Vic.), 2024-04, Vol.29 (4), p.304-311

2024

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Dyspnea in homosexual male patients: throwback to an occasionally forgotten but severe clinical presentation of HIV/AIDS

Acta clinica belgica (English ed. Online), 2020-11, Vol.75 (6), p.1-415

2020

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Azithromycin during Acute Chronic Obstructive Pulmonary Disease Exacerbations Requiring Hospitalization (BACE). A Multicenter, Randomized, Double-Blind, Placebo-controlled Trial

American journal of respiratory and critical care medicine, 2019-10, Vol.200 (7), p.857-868

2019

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Diffuse alveolar haemorrhage with predominant upper lung lobe involvement associated with congestive heart failure: a case series

Journal of thoracic disease, 2017-10, Vol.9 (10), p.3956-3960

2017

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Comparison between the ATS/ERS/JRS/ALAT criteria of 2011 and 2018 for Usual Interstitial Pneumonia on HRCT: a cross-sectional study

British journal of radiology, 2021-04, Vol.94 (1120), p.20201159-20201159

2021

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Overuse of inhaled corticosteroids in COPD: five questions for withdrawal in daily practice

International journal of chronic obstructive pulmonary disease, 2018-01, Vol.13, p.2089-2099

2018

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Human Herpes Virus 8 Unrelated Bilateral Primary Effusion Lymphoma in a Patient With Chronic Fluid Overload

Archivos de bronconeumología (English ed.), 2016-09, Vol.52 (9), p.492-493

2016

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Even if it looks like COVID-19, think again: the importance of differential diagnosis during a pandemic

Acta clinica belgica (English ed. Online), 2022-04, Vol.77 (2), p.416-420

2022

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Manual Aspiration versus Chest Tube Drainage in First Episodes of Primary Spontaneous Pneumothorax: A Multicenter, Prospective, Randomized Pilot Study

American journal of respiratory and critical care medicine, 2002-05, Vol.165 (9), p.1240-1244

2002

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Derrame linfomatoso primario bilateral, no asociado al herpesvirus humano 8, en un paciente con hipervolemia crónica

Archivos de bronconeumología, 2016-09, Vol.52 (9), p.492-493

2016

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Baseline clinical characteristics, comorbidities and prescribed medication in a real-world population of patients with idiopathic pulmonary fibrosis: the PROOF registry

BMJ open respiratory research, 2018-01, Vol.5 (1), p.e000331-e000331

2018

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Human Herpes Virus 8 Unrelated Bilateral Primary Effusion Lymphoma in a Patient With Chronic Fluid Overload

Archivos de bronconeumología (English ed.), 2016-09, Vol.52 (9), p.492-493

2016

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Quality of Life and Healthcare Resource Use in a Real-world Patient Population with Idiopathic Pulmonary Fibrosis: The PROOF Registry

Pulmonary therapy, 2022-06, Vol.8 (2), p.181-194

2022

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Predominant dendriform pulmonary ossification in a usual interstitial pneumonia-like distribution: to be distinguished from idiopathic pulmonary fibrosis

Sarcoidosis, vasculitis, and diffuse lung diseases, 2017, Vol.34 (3), p.251-256

2017

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Longitudinal clinical outcomes in a real-world population of patients with idiopathic pulmonary fibrosis: the PROOF registry

Treatment failure and hospital readmissions in severe COPD exacerbations treated with azithromycin versus placebo - a post-hoc analysis of the BACE randomized controlled trial

Diagnostic Ability of a Dynamic Multidisciplinary Discussion in Interstitial Lung Diseases

Should oral anticoagulation be discontinued after 3 months in the setting of a first high-risk pulmonary embolism secondary to a major transient/reversible risk factor?

Azithromycin for prevention of exacerbations in severe asthma (AZISAST): a multicentre randomised double-blind placebo-controlled trial

COVID-19–Associated Eosinopenia in a Patient With Chronic Eosinophilia Due to Chronic Strongyloidiasis

Diagnostic Ability of a Dynamic Multidisciplinary Discussion in Interstitial Lung Diseases: A Retrospective Observational Study of 938 Cases

Correlation of BAL Cell Count and Pulmonary Function Tests in the Era of Antifibrotics: Data From the Belgium-Luxembourg Idiopathic Pulmonary Fibrosis Registry

Correlation of BAL Cell Count and Pulmonary Function Tests in the Era of Antifibrotics

Effect of anti-interleukin drugs in patients with COVID-19 and signs of cytokine release syndrome (COV-AID): a factorial, randomised, controlled trial

Clinical course of suspected familial and sporadic idiopathic pulmonary fibrosis: Data from the PROOF‐Next registry

Dyspnea in homosexual male patients: throwback to an occasionally forgotten but severe clinical presentation of HIV/AIDS

Azithromycin during Acute Chronic Obstructive Pulmonary Disease Exacerbations Requiring Hospitalization (BACE). A Multicenter, Randomized, Double-Blind, Placebo-controlled Trial

Diffuse alveolar haemorrhage with predominant upper lung lobe involvement associated with congestive heart failure: a case series

Comparison between the ATS/ERS/JRS/ALAT criteria of 2011 and 2018 for Usual Interstitial Pneumonia on HRCT: a cross-sectional study

Overuse of inhaled corticosteroids in COPD: five questions for withdrawal in daily practice

Human Herpes Virus 8 Unrelated Bilateral Primary Effusion Lymphoma in a Patient With Chronic Fluid Overload

Even if it looks like COVID-19, think again: the importance of differential diagnosis during a pandemic

Manual Aspiration versus Chest Tube Drainage in First Episodes of Primary Spontaneous Pneumothorax: A Multicenter, Prospective, Randomized Pilot Study

Derrame linfomatoso primario bilateral, no asociado al herpesvirus humano 8, en un paciente con hipervolemia crónica

Baseline clinical characteristics, comorbidities and prescribed medication in a real-world population of patients with idiopathic pulmonary fibrosis: the PROOF registry

Human Herpes Virus 8 Unrelated Bilateral Primary Effusion Lymphoma in a Patient With Chronic Fluid Overload

Loss of GM-CSF-dependent instruction of alveolar macrophages in COVID-19 provides a rationale for inhaled GM-CSF treatment

Quality of Life and Healthcare Resource Use in a Real-world Patient Population with Idiopathic Pulmonary Fibrosis: The PROOF Registry

Predominant dendriform pulmonary ossification in a usual interstitial pneumonia-like distribution: to be distinguished from idiopathic pulmonary fibrosis

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