Treating sleep-disordered breathing of idiopathic pulmonary fibrosis patients with CPAP and nocturnal oxygen treatment. A pilot study
Authors (first, second and last of 12)
Collection
Pulmonary fibrosis: new insights
The field of pulmonary fibrosis has gone through substantial changes in recent years, with several traditional views on disease pathogenesis and treatment being challenged and replaced by more convincing concepts. The collection seeks manuscripts that address the diagnosis, characterization and management of pulmonary fibrosis, with emphasis on novel concepts of disease pathogenesis, predictors of disease behavior and response to treatment and developmental drugs.
Articles (15 in this collection)
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Clinical, radiological and histopathological features of patients with familial pulmonary fibrosis
Authors (first, second and last of 10)
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Disease trajectories in interstitial lung diseases – data from the EXCITING-ILD registry
Authors (first, second and last of 24)
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Psoriasis may increase the risk of idiopathic pulmonary fibrosis: a two-sample Mendelian randomization study
Authors (first, second and last of 5)
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Association of musculoskeletal involvement with lung function and mortality in patients with idiopathic pulmonary fibrosis
Authors (first, second and last of 10)
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Phenotypic subtypes of fibrotic hypersensitivity pneumonitis identified by machine learning consensus clustering analysis
Authors (first, second and last of 6)
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Hospitalisation patterns in interstitial lung diseases: data from the EXCITING-ILD registry
Authors (first, second and last of 24)
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Tuftelin1 drives experimental pulmonary fibrosis progression by facilitating stress fiber assembly
Authors (first, second and last of 14)
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The causal relationship between physical activity, sedentary time and idiopathic pulmonary fibrosis risk: a Mendelian randomization study
Authors (first, second and last of 9)
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Expression of PD-1/PD-L1 axis in mediastinal lymph nodes and lung tissue of human and experimental lung fibrosis indicates a potential therapeutic target for idiopathic pulmonary fibrosis
Authors (first, second and last of 22)
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Differentiating interstitial lung diseases from other respiratory diseases using electronic nose technology
Authors (first, second and last of 7)
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Usefulness of FAPα assessment in bronchoalveolar lavage as a marker of fibrogenesis: results of a preclinical study and first report in patients with idiopathic pulmonary fibrosis
Authors (first, second and last of 17)
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Lung immune signatures define two groups of end-stage IPF patients
Authors (first, second and last of 12)
