HRCT diagnosis of diffuse parenchymal lung disease: inter-observer variation. - Wikidata - wikimedia - TriplyDB

HRCT diagnosis of diffuse parenchymal lung disease: inter-observer variation.

HRCT diagnosis of diffuse parenchymal lung disease: inter-observer variation.

http://www.wikidata.org/entity/Q35536734

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Personalized medicine: applying 'omics' to lung fibrosis An official American Thoracic Society/European Respiratory Society statement: Update of the international multidisciplinary classification of the idiopathic interstitial pneumonias Automated 3D ιnterstitial lung disease εxtent quantification: performance evaluation and correlation to PFTs 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.Lung texture in serial thoracic CT scans: correlation with radiologist-defined severity of acute changes following radiation therapy A sparse representation based method to classify pulmonary patterns of diffuse lung diseases.Evaluating the interstitial lung disease multidisciplinary meeting: a survey of expert centres.Lung texture in serial thoracic CT scans: assessment of change introduced by image registration.Update in diffuse parenchymal lung diseases 2005.Diagnostic approach to interstitial pneumonias in a single centre: report on 88 cases.Interstitial lung disease--the new synergy between radiology and pathology.The current position of surgical lung biopsy in the diagnosis of idiopathic pulmonary fibrosis.The diagnosis and treatment of idiopathic pulmonary fibrosis Inter- and intraobserver variation between radiologists in the detection of abnormal parenchymal lung changes on high-resolution computed tomography.Differentiating between IPF and NSIP.Fibrosing interstitial lung disease. A practical high-resolution computed tomography-based approach to diagnosis and management and a review of the literature.Agreement and mortality prediction in high-resolution CT of diffuse fibrotic lung disease.Estimating the incidence of interstitial lung diseases in the Cree of Eeyou Istchee, northern Québec.Diagnostic accuracy of a clinical diagnosis of idiopathic pulmonary fibrosis: an international case-cohort study.Deep-inspiration breath-hold 18F-FDG-PET/CT is useful for assessment of connective tissue disease associated interstitial pneumonia.Automated Lung Segmentation from HRCT Scans with Diffuse Parenchymal Lung Diseases What is this thing called CFA?The clinical impact of high resolution computed tomography in patients with respiratory disease.The clinical utility of bronchoalveolar lavage cellular analysis in interstitial lung disease.Fibrotic idiopathic interstitial pneumonias: HRCT findings that predict mortality.Inflammatory activity is still present in the advanced stages of idiopathic pulmonary fibrosis.The predictive prognostic factors for polymyositis/dermatomyositis-associated interstitial lung disease.The interstitial lung disease multidisciplinary meeting: A position statement from the Thoracic Society of Australia and New Zealand and the Lung Foundation Australia.Do high-resolution CT findings of usual interstitial pneumonitis obviate lung biopsy? Views of pulmonologists.Interobserver agreement on the diagnosis of bowel ischemia: assessment using dynamic computed tomography of small bowel obstruction.Quantitative CT indexes are significantly associated with exercise oxygen desaturation in interstitial lung disease related to systemic sclerosis.Significance of bronchoalveolar lavage for the diagnosis of idiopathic pulmonary fibrosis.Texture classification-based segmentation of lung affected by interstitial pneumonia in high-resolution CT.Observer agreement in the diagnosis of interstitial lung diseases based on HRCT scans.Interobserver reliability of the chest radiograph in pulmonary embolism.Functional predictors of exertional dyspnea, 6-min walking distance and HRCT fibrosis score in idiopathic pulmonary fibrosis.High-resolution computed tomography in idiopathic pulmonary fibrosis: diagnosis and prognosis.Histopathologic diagnosis in diffuse lung disease: an ailing gold standard.Interobserver reliability in describing radiographic lung changes after stereotactic body radiation therapy

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P2860

HRCT diagnosis of diffuse parenchymal lung disease: inter-observer variation.

http://www.wikidata.org/entity/Q35536734

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HRCT diagnosis of diffuse parenchymal lung disease: inter-observer variation.

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HRCT diagnosis of diffuse parenchymal lung disease: inter-observer variation.

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HRCT diagnosis of diffuse parenchymal lung disease: inter-observer variation.

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HRCT diagnosis of diffuse parenchymal lung disease: inter-observer variation

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A U Wells

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P2860

American Thoracic Society/European Respiratory Society International Multidisciplinary Consensus Classification of the Idiopathic Interstitial Pneumonias. This joint statement of the American Thoracic Society (ATS), and the European Respiratory Soci

High-resolution CT of the lungs.

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

Chronic diffuse infiltrative lung disease: comparison of diagnostic accuracy of CT and chest radiography.

Measurement of observer agreement.

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

Computed tomography of air-space disease.

How medical professionals evaluate expressions of probability.

The predictive value of appearances on thin-section computed tomography in fibrosing alveolitis.

Importance of ground-glass attenuation in chronic diffuse infiltrative lung disease: pathologic-CT correlation.

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