Usual Interstitial Pneumonia Can Be Detected in Transbronchial Biopsies Using Machine Learning
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D. Lynch | F. Martinez | G. Raghu | G. Kennedy | T. Colby | D. Pankratz | J. Myers | Yoonha Choi | U. Imtiaz | G. Fedorowicz | Jessica D Anderson | K. Brown | K. Flaherty | M. Steele | S. Groshong | N. Barth | Sean P. Walsh | Jing Huang | Jessica D. Anderson | Sean Walsh | J. Myers
[1] J. Myers,et al. Idiopathic pulmonary fibrosis: clinical relevance of pathologic classification. , 1998, American journal of respiratory and critical care medicine.
[2] K P Offord,et al. Prognostic significance of histopathologic subsets in idiopathic pulmonary fibrosis. , 1998, American journal of respiratory and critical care medicine.
[3] G. Raghu,et al. The accuracy of the clinical diagnosis of new-onset idiopathic pulmonary fibrosis and other interstitial lung disease: A prospective study. , 1999, Chest.
[4] R. Strawderman,et al. Histopathologic variability in usual and nonspecific interstitial pneumonias. , 2001, American journal of respiratory and critical care medicine.
[5] A. Katzenstein,et al. Usual Interstitial Pneumonia: Histologic Study of Biopsy and Explant Specimens , 2002, The American journal of surgical pathology.
[6] A. Nicholson,et al. The relationship between individual histologic features and disease progression in idiopathic pulmonary fibrosis. , 2002, American journal of respiratory and critical care medicine.
[7] R. Strawderman,et al. Clinical significance of histological classification of idiopathic interstitial pneumonia , 2002, European Respiratory Journal.
[8] Paul J. Friedman,et al. 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 Society (ERS) was adopted by the ATS board of directors , 2002, American journal of respiratory and critical care medicine.
[9] F. Martinez,et al. Radiological versus histological diagnosis in UIP and NSIP: survival implications , 2003, Thorax.
[10] Susan Murray,et al. Idiopathic interstitial pneumonia: what is the effect of a multidisciplinary approach to diagnosis? , 2004, American journal of respiratory and critical care medicine.
[11] Hiroaki Kitano,et al. The PANTHER database of protein families, subfamilies, functions and pathways , 2004, Nucleic Acids Res..
[12] Naftali Kaminski,et al. Gene expression profiles distinguish idiopathic pulmonary fibrosis from hypersensitivity pneumonitis. , 2006, American journal of respiratory and critical care medicine.
[13] A. Katzenstein,et al. Transbronchial biopsy in usual interstitial pneumonia. , 2006, Chest.
[14] J. Myers,et al. Role of surgical lung biopsy in separating chronic hypersensitivity pneumonia from usual interstitial pneumonia/idiopathic pulmonary fibrosis: analysis of 31 biopsies from 15 patients. , 2008, Chest.
[15] S. Mukhopadhyay,et al. Diagnosis of usual interstitial pneumonia and distinction from other fibrosing interstitial lung diseases. , 2008, Human pathology.
[16] N. Müller,et al. Computed tomography findings in pathological usual interstitial pneumonia: relationship to survival. , 2008, American journal of respiratory and critical care medicine.
[17] Y. Eishi,et al. Histopathologic analysis of sixteen autopsy cases of chronic hypersensitivity pneumonitis and comparison with idiopathic pulmonary fibrosis/usual interstitial pneumonia. , 2009, American journal of clinical pathology.
[18] Trevor Hastie,et al. Regularization Paths for Generalized Linear Models via Coordinate Descent. , 2010, Journal of statistical software.
[19] Sharon Sanderson,et al. Gene set analysis of lung samples provides insight into pathogenesis of progressive, fibrotic pulmonary sarcoidosis. , 2010, American journal of respiratory and critical care medicine.
[20] H. Shim,et al. Histopathologic findings of transbronchial biopsy in usual interstitial pneumonia , 2010, Pathology international.
[21] Takeshi Johkoh,et al. American Thoracic Society Documents An Official ATS / ERS / JRS / ALAT Statement : Idiopathic Pulmonary Fibrosis : Evidence-based Guidelines for Diagnosis and Management , 2011 .
[22] O. Nanni,et al. Transbronchial biopsy is useful in predicting UIP pattern , 2012, Respiratory Research.
[23] Shandra L. Protzko,et al. An official American Thoracic Society/European Respiratory Society statement: Update of the international multidisciplinary classification of the idiopathic interstitial pneumonias. , 2013, American journal of respiratory and critical care medicine.
[24] M. Selman,et al. Revealing the pathogenic and aging-related mechanisms of the enigmatic idiopathic pulmonary fibrosis. an integral model. , 2014, American journal of respiratory and critical care medicine.
[25] W. Huber,et al. Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2 , 2014, Genome Biology.
[26] Naftali Kaminski,et al. A novel genomic signature with translational significance for human idiopathic pulmonary fibrosis. , 2015, American journal of respiratory cell and molecular biology.
[27] Y. Sugiyama,et al. Diagnostic certainty of idiopathic pulmonary fibrosis/usual interstitial pneumonia: The effect of the integrated clinico-radiological assessment. , 2015, European journal of radiology.
[28] Ed Y. Tom,et al. Classification of usual interstitial pneumonia in patients with interstitial lung disease: assessment of a machine learning approach using high-dimensional transcriptional data. , 2015, The Lancet. Respiratory medicine.
[29] T. Welte,et al. Molecular Profiling in Lung Biopsies of Human Pulmonary Allografts to Predict Chronic Lung Allograft Dysfunction. , 2015, The American journal of pathology.
[30] A. Aggarwal,et al. Diagnostic Yield and Safety of Cryoprobe Transbronchial Lung Biopsy in Diffuse Parenchymal Lung Diseases: Systematic Review and Meta-Analysis , 2016, Respiratory Care.
[31] F. Martinez,et al. Plasma Surfactant Protein-D, Matrix Metalloproteinase-7, and Osteopontin Index Distinguishes Idiopathic Pulmonary Fibrosis from Other Idiopathic Interstitial Pneumonias. , 2016, American journal of respiratory and critical care medicine.
[32] A. Nicholson,et al. Multicentre evaluation of multidisciplinary team meeting agreement on diagnosis in diffuse parenchymal lung disease: a case-cohort study. , 2016, The Lancet. Respiratory medicine.
[33] G. Rossi,et al. Bronchoscopic Lung Cryobiopsy Increases Diagnostic Confidence in the Multidisciplinary Diagnosis of Idiopathic Pulmonary Fibrosis. , 2016, American journal of respiratory and critical care medicine.
[34] M. Mejía,et al. Increased Expression of CC16 in Patients with Idiopathic Pulmonary Fibrosis , 2016, PloS one.
[35] V. Poletti,et al. Invasive diagnostic techniques in idiopathic interstitial pneumonias , 2016, Respirology.