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Interstitial lung disease in scleroderma

Rheumatic Disease Clinics of North America, 2003
Pulmonary fibrosis occurs most patients who have scleroderma. It progresses to severe restrictive lung disease in about 15% of patients and remains a major cause of death in this disease. Risks for developing pulmonary fibrosis include diffuse cutaneous scleroderma and anti-Scl-70 antibodies, and risks for developing progressive pulmonary fibrosis and ...
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An Introduction to the Interstitial Lung Diseases

Clinics in Chest Medicine, 1982
The interstitial lung diseases are a heterogeneous group of disorders that have similar clinical, roentgenographic, and physiologic features. The histopathology of most is characterized by an alveolitis and alveolar septal fibrosis. Current concepts are that connective tissue alterations are preceded and caused by the alveolitis.
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Comprehensive Analysis of Fibroblast Activation Protein Expression in Interstitial Lung Diseases

American Journal of Respiratory and Critical Care Medicine, 2023
Jinhe Zhang
exaly  

Acute Exacerbations of Interstitial Lung Diseases: Focus on Biomarkers

International Journal of Molecular Sciences, 2023
Paschalis Steiropoulos   +1 more
exaly  

Impact of Lung Biopsy Information on Treatment Strategy of Patients with Interstitial Lung Diseases

Annals of the American Thoracic Society, 2022
Sara Piciucchi   +2 more
exaly  

Recent Advances of Artificial Intelligence Applications in Interstitial Lung Diseases

Diagnostics, 2023
Konstantinos Exarchos   +1 more
exaly  

Interstitial Lung Diseases and the Impact of Gender

Clinics in Chest Medicine, 2021
Argyris Tzouvelekis   +2 more
exaly  

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