Search Results - "Collard, R"
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Idiopathic pulmonary fibrosis
Published in The Lancet (British edition) (13-05-2017)“…Summary Idiopathic pulmonary fibrosis is a prototype of chronic, progressive, and fibrotic lung disease. Healthy tissue is replaced by altered extracellular…”
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Pathogenesis of idiopathic pulmonary fibrosis
Published in Annual review of pathology (01-01-2014)“…Idiopathic pulmonary fibrosis (IPF) is a fibrosing interstitial lung disease associated with aging that is characterized by the histopathological pattern of…”
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Clinical Course and Prediction of Survival in Idiopathic Pulmonary Fibrosis
Published in American journal of respiratory and critical care medicine (15-02-2011)“…Idiopathic pulmonary fibrosis (IPF) is a progressive, life-threatening, interstitial lung disease of unknown etiology. The median survival of patients with IPF…”
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Efficacy of Nintedanib in Idiopathic Pulmonary Fibrosis across Prespecified Subgroups in INPULSIS
Published in American journal of respiratory and critical care medicine (15-01-2016)“…In the two replicate, placebo-controlled, 52-week, phase III INPULSIS trials, nintedanib 150 mg twice daily significantly reduced the annual rate of decline in…”
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5
Telomere-related lung fibrosis is diagnostically heterogeneous but uniformly progressive
Published in The European respiratory journal (01-12-2016)“…Heterozygous mutations in four telomere-related genes have been linked to pulmonary fibrosis, but little is known about similarities or differences of affected…”
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Idiopathic pulmonary fibrosis in US Medicare beneficiaries aged 65 years and older: incidence, prevalence, and survival, 2001–11
Published in The lancet respiratory medicine (01-07-2014)“…Summary Background Published data for the epidemiology of idiopathic pulmonary fibrosis in the USA are scarce. We sought to estimate the incidence, prevalence,…”
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Molecular biomarkers in idiopathic pulmonary fibrosis
Published in American journal of physiology. Lung cellular and molecular physiology (01-11-2014)“…Molecular biomarkers are highly desired in idiopathic pulmonary fibrosis (IPF), where they hold the potential to elucidate underlying disease mechanisms,…”
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Management of Myositis-Related Interstitial Lung Disease
Published in Chest (01-11-2016)“…Interstitial lung disease (ILD) is a frequent pulmonary manifestation and an important cause of morbidity and mortality in patients with idiopathic…”
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Use of Mycophenolate Mofetil or Azathioprine for the Management of Chronic Hypersensitivity Pneumonitis
Published in Chest (01-03-2017)“…Background The treatment of chronic hypersensitivity pneumonitis (cHP) often includes systemic oral corticosteroids, but the optimal pharmacologic management…”
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Efficacy and Safety of Nintedanib in Idiopathic Pulmonary Fibrosis
Published in The New England journal of medicine (29-05-2014)“…In this randomized, placebo-controlled trial, treatment with nintedanib, an intracellular inhibitor of multiple tyrosine kinases, led to a reduced rate of loss…”
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11
Acute exacerbation of idiopathic pulmonary fibrosis: shifting the paradigm
Published in The European respiratory journal (01-08-2015)“…The goal of this review is to summarise the clinical features, management, and prognosis of acute exacerbations of idiopathic pulmonary fibrosis (AE-IPF)…”
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Acute Exacerbation of Idiopathic Pulmonary Fibrosis. An International Working Group Report
Published in American journal of respiratory and critical care medicine (01-08-2016)“…Acute exacerbation of idiopathic pulmonary fibrosis has been defined as an acute, clinically significant, respiratory deterioration of unidentifiable cause…”
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An Official ATS/ERS/JRS/ALAT Clinical Practice Guideline: Treatment of Idiopathic Pulmonary Fibrosis. An Update of the 2011 Clinical Practice Guideline
Published in American journal of respiratory and critical care medicine (15-07-2015)“…This document updates the American Thoracic Society/European Respiratory Society/Japanese Respiratory Society/Latin American Thoracic Association guideline on…”
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Pathologic Findings and Prognosis in a Large Prospective Cohort of Chronic Hypersensitivity Pneumonitis
Published in Chest (01-09-2017)“…The ability of specific histopathologic features to predict mortality or lung transplantation in patients with chronic hypersensitivity pneumonitis (HP) is…”
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Staging of idiopathic pulmonary fibrosis: past, present and future
Published in European respiratory review (01-06-2014)“…Idiopathic pulmonary fibrosis (IPF) is traditionally staged with terms such as "mild", "severe", "early" and "advanced" based on pulmonary function tests. This…”
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Heterogeneity in Unclassifiable Interstitial Lung Disease. A Systematic Review and Meta-Analysis
Published in Annals of the American Thoracic Society (01-07-2018)“…Accurate diagnosis of interstitial lung disease is necessary to identify the most appropriate management strategy and to inform prognosis. Many patients cannot…”
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Clinical Features and Outcomes in Combined Pulmonary Fibrosis and Emphysema in Idiopathic Pulmonary Fibrosis
Published in Chest (01-07-2013)“…Background Combined pulmonary fibrosis and emphysema (CPFE) is increasingly recognized, but its prevalence and prognosis remain unclear. We sought to determine…”
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Acute exacerbations in the INPULSIS trials of nintedanib in idiopathic pulmonary fibrosis
Published in The European respiratory journal (01-05-2017)“…Time to first investigator-reported acute exacerbation was a key secondary end-point in the INPULSIS trials of nintedanib in patients with idiopathic pulmonary…”
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A Standardized Diagnostic Ontology for Fibrotic Interstitial Lung Disease. An International Working Group Perspective
Published in American journal of respiratory and critical care medicine (15-11-2017)“…[...]there is frequent reluctance to perform surgical lung biopsy in patients with clinically unclassifiable ILD due to safety concerns. [...]it should…”
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Variability in Global Prevalence of Interstitial Lung Disease
Published in Frontiers in medicine (04-11-2021)“…There are limited epidemiologic studies describing the global burden and geographic heterogeneity of interstitial lung disease (ILD) subtypes. We found that…”
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