Review Series: Aspects of Interstitial lung disease: Differentiating between IPF and NSIP
Author:
Affiliation:
1. Department of Allergy, Immunology and Respiratory Medicine, Alfred Hospital, Melbourne, Australia
2. Department of Respiratory Medicine, Austin Hospital, Melbourne, Australia,
Abstract
Publisher
SAGE Publications
Subject
Pulmonary and Respiratory Medicine
Link
http://journals.sagepub.com/doi/pdf/10.1177/1479972310376205
Reference56 articles.
1. American Thoracic Society/European Respiratory Society International Multidisciplinary Consensus Classification of the Idiopathic Interstitial Pneumonias
2. Beyond a consensus classification for idiopathic interstitial pneumonias: progress and controversies
3. Idiopathic Pulmonary Fibrosis: Diagnosis and Treatment
4. Predicting Survival in Idiopathic Pulmonary Fibrosis
5. Prognostic Significance of Histopathologic Subsets in Idiopathic Pulmonary Fibrosis
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1. An integrated study fusing systems biology and machine learning algorithms for genome-based discrimination of IPF and NSIP diseases: a new approach to the diagnostic challenge;Soft Computing;2023-11-11
2. Cell-Specific Response of NSIP- and IPF-Derived Fibroblasts to the Modification of the Elasticity, Biological Properties, and 3D Architecture of the Substrate;International Journal of Molecular Sciences;2022-11-25
3. Discrimination between NSIP- and IPF-Derived Fibroblasts Based on Multi-Parameter Characterization of Their Growth, Morphology and Physic-Chemical Properties;International Journal of Molecular Sciences;2022-02-15
4. Mimics of Idiopathic Pulmonary Fibrosis;Respiratory Medicine;2018-12-15
5. Serum AGE/RAGEs as potential biomarker in idiopathic pulmonary fibrosis;Respiratory Research;2018-11-08
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