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Pulmonary alveolar proteinosis

Respirology (Carlton, Vic.), 2020-08, Vol.25 (8), p.816-826

2020

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Combined anti-fibrotic and anti-inflammatory properties of JAK-inhibitors on macrophages in vitro and in vivo: Perspectives for scleroderma-associated interstitial lung disease

Biochemical pharmacology, 2020-08, Vol.178, p.114103, Article 114103

2020

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To be malnourished or not to be malnourished: that is the question

The European respiratory journal, 2022-01, Vol.59 (1), p.2102455

2022

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Impaired efferocytosis and neutrophil extracellular trap clearance by macrophages in ARDS

The European respiratory journal, 2018-08, Vol.52 (2), p.1702590

2018

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Malnutrition in idiopathic pulmonary fibrosis: the great forgotten comorbidity

The European respiratory journal, 2019-05, Vol.53 (5), p.1900418

2019

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Efficacy and safety of nintedanib in patients with advanced idiopathic pulmonary fibrosis

BMC pulmonary medicine, 2020-01, Vol.20 (1), p.3-3, Article 3

2020

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Sirolimus-Induced Pulmonary Alveolar Proteinosis in the Context of Hematopoietic Stem Cells Transplant Rejection: A Case Report

Transplantation proceedings, 2022-01, Vol.54 (1), p.180-184

2022

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Analysis of body mass index, weight loss and progression of idiopathic pulmonary fibrosis

Respiratory research, 2020-11, Vol.21 (1), p.1-312, Article 312

2020

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High-flow nasal oxygen: a safe, efficient treatment for COVID-19 patients not in an ICU

The European respiratory journal, 2020-11, Vol.56 (5), p.2001154

2020

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Alteration of human macrophage phenotypes by the anti-fibrotic drug nintedanib

International immunopharmacology, 2019-07, Vol.72, p.112-123

2019

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TNF-α and IL-10 Control CXCL13 Expression in Human Macrophages

The Journal of immunology (1950), 2020-05, Vol.204 (9), p.2492-2502

2020

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Pharmacological management of progressive-fibrosing interstitial lung diseases: a review of the current evidence

European respiratory review, 2018-12, Vol.27 (150), p.180074

2018

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Incidence of Pneumocystis jiroveci Pneumonia among Groups at Risk in HIV-negative Patients

The American journal of medicine, 2014-12, Vol.127 (12), p.1242.e11-1242.e17

2014

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Diagnosis of Pneumocystis jirovecii pneumonia in immunocompromised patients by real-time PCR: a 4-year prospective study

Journal of clinical microbiology, 2014-09, Vol.52 (9), p.3370-3376

2014

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Unmet needs in the treatment of idiopathic pulmonary fibrosis-insights from patient chart review in five European countries

BMC pulmonary medicine, 2017-09, Vol.17 (1), p.124-12, Article 124

2017

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What are the best indicators to assess malnutrition in idiopathic pulmonary fibrosis patients? A cross-sectional study in a referral center

Nutrition (Burbank, Los Angeles County, Calif.), 2019-06, Vol.62, p.115-121

2019

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Women and COPD: do we need more evidence?

European respiratory review, 2019-03, Vol.28 (151), p.180055

2019

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Estimates of epidemiology, mortality and disease burden associated with progressive fibrosing interstitial lung disease in France (the PROGRESS study)

Respiratory research, 2021-05, Vol.22 (1), p.1-162, Article 162

2021

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M1/M2 polarisation state of M-CSF blood-derived macrophages in systemic sclerosis

Annals of the rheumatic diseases, 2019-11, Vol.78 (11), p.e127

2019

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Soluble CD163 is produced by monocyte-derived and alveolar macrophages, and is not associated with the severity of idiopathic pulmonary fibrosis

Innate immunity (London, England), 2022-04, Vol.28 (3-4), p.138-151

2022

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The natural history of adult pulmonary Langerhans cell histiocytosis: a prospective multicentre study

Orphanet journal of rare diseases, 2015-03, Vol.10 (1), p.30-30, Article 30

2015

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Weight loss and outcomes in subjects with progressive pulmonary fibrosis: data from the INBUILD trial

Respiratory research, 2023-03, Vol.24 (1), p.71-71, Article 71

2023

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Intrapleural use of urokinase and DNase in pleural infections managed with repeated thoracentesis: A comparative cohort study

PloS one, 2021-09, Vol.16 (9), p.e0257339-e0257339

2021

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Is it about what comes in or what goes out? A reply to Sesé et al., 2021

Respiratory medicine, 2022-01, Vol.191, p.106715-106715, Article 106715

2022

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Role of serum immunoglobulins for predicting sarcoidosis outcome: A cohort study

PloS one, 2018-04, Vol.13 (4), p.e0193122-e0193122

2018

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Pulmonary alveolar proteinosis

Combined anti-fibrotic and anti-inflammatory properties of JAK-inhibitors on macrophages in vitro and in vivo: Perspectives for scleroderma-associated interstitial lung disease

To be malnourished or not to be malnourished: that is the question

Impaired efferocytosis and neutrophil extracellular trap clearance by macrophages in ARDS

Malnutrition in idiopathic pulmonary fibrosis: the great forgotten comorbidity

Efficacy and safety of nintedanib in patients with advanced idiopathic pulmonary fibrosis

Sirolimus-Induced Pulmonary Alveolar Proteinosis in the Context of Hematopoietic Stem Cells Transplant Rejection: A Case Report

Analysis of body mass index, weight loss and progression of idiopathic pulmonary fibrosis

High-flow nasal oxygen: a safe, efficient treatment for COVID-19 patients not in an ICU

Alteration of human macrophage phenotypes by the anti-fibrotic drug nintedanib

TNF-α and IL-10 Control CXCL13 Expression in Human Macrophages

Pharmacological management of progressive-fibrosing interstitial lung diseases: a review of the current evidence

Incidence of Pneumocystis jiroveci Pneumonia among Groups at Risk in HIV-negative Patients

Diagnosis of Pneumocystis jirovecii pneumonia in immunocompromised patients by real-time PCR: a 4-year prospective study

Unmet needs in the treatment of idiopathic pulmonary fibrosis-insights from patient chart review in five European countries

What are the best indicators to assess malnutrition in idiopathic pulmonary fibrosis patients? A cross-sectional study in a referral center

Women and COPD: do we need more evidence?

Estimates of epidemiology, mortality and disease burden associated with progressive fibrosing interstitial lung disease in France (the PROGRESS study)

M1/M2 polarisation state of M-CSF blood-derived macrophages in systemic sclerosis

Soluble CD163 is produced by monocyte-derived and alveolar macrophages, and is not associated with the severity of idiopathic pulmonary fibrosis

The natural history of adult pulmonary Langerhans cell histiocytosis: a prospective multicentre study

Weight loss and outcomes in subjects with progressive pulmonary fibrosis: data from the INBUILD trial

Intrapleural use of urokinase and DNase in pleural infections managed with repeated thoracentesis: A comparative cohort study

Is it about what comes in or what goes out? A reply to Sesé et al., 2021

Role of serum immunoglobulins for predicting sarcoidosis outcome: A cohort study

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