Radiological versus histological diagnosis in UIP and NSIP: survival implications. - Wikidata - wikimedia - TriplyDB

Radiological versus histological diagnosis in UIP and NSIP: survival implications.

Radiological versus histological diagnosis in UIP and NSIP: survival implications.

http://www.wikidata.org/entity/Q35535697

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A micro RNA processing defect in rapidly progressing idiopathic pulmonary fibrosis Idiopathic pulmonary fibrosis.Classification and natural history of the idiopathic interstitial pneumonias Serum biomarkers in interstitial lung diseases Management of Rheumatoid Arthritis Patients with Interstitial Lung Disease: Safety of Biological Antirheumatic Drugs and Assessment of Pulmonary Fibrosis Statin-induced lung injury: diagnostic clue and outcome A practical approach to high-resolution CT of diffuse lung disease Personalized medicine: applying 'omics' to lung fibrosis A roadmap to promote clinical and translational research in rheumatoid arthritis-associated interstitial lung disease Diagnosis of idiopathic pulmonary fibrosis: Current issues.Computed tomography findings in pathological usual interstitial pneumonia: relationship to survival Idiopathic interstitial pneumonia: what is the effect of a multidisciplinary approach to diagnosis?An official American Thoracic Society/European Respiratory Society statement: Update of the international multidisciplinary classification of the idiopathic interstitial pneumonias An official ATS/ERS/JRS/ALAT statement: idiopathic pulmonary fibrosis: evidence-based guidelines for diagnosis and management Predicting pulmonary fibrosis disease course from past trends in pulmonary function.High-resolution CT of complications of idiopathic fibrotic lung disease Clinical advances in the diagnosis and therapy of the interstitial lung diseases.Is there a uniform approach to the management of diffuse parenchymal lung disease (DPLD) in the UK? A national benchmarking exercise.Inter-observer variation between pathologists in diffuse parenchymal lung disease.Clinical predictors of a diagnosis of idiopathic pulmonary fibrosis.Idiopathic interstitial pneumonias: progress in classification, diagnosis, pathogenesis and management Rheumatoid arthritis-associated interstitial lung disease: radiologic identification of usual interstitial pneumonia pattern.CT scan findings of probable usual interstitial pneumonitis have a high predictive value for histologic usual interstitial pneumonitis Influence of autoimmune biomarkers on interstitial lung diseases: A tertiary referral center based case-control study.Cardiovascular involvement in connective tissue disease: the role of interstitial lung disease The vitronectin-binding function of PAI-1 exacerbates lung fibrosis in mice.HRCT diagnosis of diffuse parenchymal lung disease: inter-observer variation.Angiogenic cytokines in patients with idiopathic interstitial pneumonia.Therapeutic targeting of CC ligand 21 or CC chemokine receptor 7 abrogates pulmonary fibrosis induced by the adoptive transfer of human pulmonary fibroblasts to immunodeficient mice.Focal interstitial CC chemokine receptor 7 (CCR7) expression in idiopathic interstitial pneumonia.Plakoglobin expression in fibroblasts and its role in idiopathic pulmonary fibrosis.Idiopathic pulmonary fibrosis: current understanding of the pathogenesis and the status of treatment Clinical features of rheumatoid arthritis-associated interstitial lung disease.Treatment of idiopathic pulmonary fibrosis: is there anything new?Back to the future: historical perspective on the pathogenesis of idiopathic pulmonary fibrosis.Challenges in pulmonary fibrosis x 5: the NSIP/UIP debate.Interferon gamma-1b in the treatment of idiopathic pulmonary fibrosis.Idiopathic pulmonary fibrosis : new concepts in pathogenesis and implications for drug therapy High-resolution CT scan findings in familial interstitial pneumonia do not conform to those of idiopathic interstitial pneumonia Update in diffuse parenchymal lung diseases 2005.

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P2860

Radiological versus histological diagnosis in UIP and NSIP: survival implications.

http://www.wikidata.org/entity/Q35535697

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2003 nî lūn-bûn

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2003年の論文

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2003年論文

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Radiological versus histological diagnosis in UIP and NSIP: survival implications.

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Radiological versus histological diagnosis in UIP and NSIP: survival implications.

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Radiological versus histological diagnosis in UIP and NSIP: survival implications.

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Radiological versus histological diagnosis in UIP and NSIP: survival implications.

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Radiological versus histological diagnosis in UIP and NSIP: survival implications

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P2860

Clinical usefulness of high resolution computed tomography in cryptogenic fibrosing alveolitis.

Idiopathic nonspecific interstitial pneumonia: prognostic significance of cellular and fibrosing patterns: survival comparison with usual interstitial pneumonia and desquamative interstitial pneumonia.

The interstitial pneumonias: understanding the acronyms.

Idiopathic pulmonary fibrosis: clinical relevance of pathologic classification.

Nonspecific interstitial pneumonia. Individualization of a clinicopathologic entity in a series of 12 patients.

Colchicine versus prednisone in the treatment of idiopathic pulmonary fibrosis. A randomized prospective study. Members of the Lung Study Group.

Serial computed tomographic evaluation in desquamative interstitial pneumonia.

Accuracy of the typical computed tomographic appearances of fibrosing alveolitis

Interpretation of Emergency Department radiographs: a comparison of emergency medicine physicians with radiologists, residents with faculty, and film with digital display.

Interstitial lung disease: a diagnostic approach. Are CT scan and lung biopsy indicated in every patient?

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