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Lancet Respiratory Medicine, The, ISSN 2213-2600, 2016, Volume 4, Issue 9, pp. 708 - 719
Journal Article
Chest, ISSN 0012-3692, 07/2017, Volume 152, Issue 1, pp. 103 - 112
Background Some patients with autoimmune characteristics and idiopathic interstitial pneumonia, particularly usual interstitial pneumonia (UIP), do not fit... 
interstitial pneumonia with autoimmune features | idiopathic pulmonary fibrosis | interstitial lung disease | autoimmune interstitial lung disease | CRITERIA | DIAGNOSIS | SCLERODERMA LUNG | PROGNOSIS | HEALTHY ELDERLY POPULATION | CONNECTIVE-TISSUE DISEASE | PREVALENCE | AUTOIMMUNE FEATURES | RESPIRATORY SYSTEM | LUNG-DISEASE | PULMONARY-FIBROSIS | CRITICAL CARE MEDICINE | Follow-Up Studies | Autoantibodies - blood | Humans | Middle Aged | Idiopathic Interstitial Pneumonias - diagnosis | Tomography, X-Ray Computed - methods | Male | Lung - diagnostic imaging | Statistics as Topic | Washington - epidemiology | Lung Diseases, Interstitial - diagnosis | Autoimmunity - immunology | Idiopathic Interstitial Pneumonias - physiopathology | Female | Lung Diseases, Interstitial - physiopathology | Needs Assessment | Connective Tissue Diseases - physiopathology | Diagnosis, Differential | Respiratory Function Tests - methods | Connective Tissue Diseases - diagnosis | Lung - physiopathology | Idiopathic Pulmonary Fibrosis - immunology | Idiopathic Interstitial Pneumonias - epidemiology | Lung Diseases, Interstitial - immunology | Idiopathic Pulmonary Fibrosis - diagnosis | Aged | Idiopathic Pulmonary Fibrosis - physiopathology | Cohort Studies | Idiopathic Interstitial Pneumonias - immunology | Autoantibodies | Pulmonary fibrosis | Health aspects | Analysis | Patient outcomes | Risk factors | Index Medicus | Abridged Index Medicus | UIP, usual interstitial pneumonia | IP, interstitial pneumonia | ILD, interstitial lung disease | UWMC, University of Washington Medical Center | PFT, pulmonary function test | CILD, Center for Interstitial Lung Diseases | AI-ILD, autoimmune interstitial lung disease | CTD, connective tissue disease | IPF, idiopathic pulmonary fibrosis | CTD-ILD, connective tissue disease-associated interstitial lung disease | NSIP, nonspecific interstitial pneumonia | IPAF, interstitial pneumonia with autoimmune features | Lone-IPF, IPF with negative CTD serologies | Dlco, diffusion capacity | Diffuse Lung Disease
Journal Article
Journal Article
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 06/2013, Volume 368, Issue 23, pp. 2192 - 2200
Journal Article
Rheumatology (United Kingdom), ISSN 1462-0324, 2014, Volume 53, Issue 9, pp. 1676 - 1682
Journal Article
Journal Article
Chest, ISSN 0012-3692, 2016, Volume 151, Issue 2, pp. 389 - 399
Background Surgical lung biopsy (SLB) is invasive and not possible in all patients with undiagnosed interstitial lung disease (ILD). We hypothesized that... 
Pulmonary/Respiratory | idiopathic pulmonary fibrosis | interstitial lung disease | lung biopsy | idiopathic interstitial pneumonia | MORTALITY | MANAGEMENT | EFFICACY | SAFETY | CLASSIFICATION | PNEUMONIA | CRYOBIOPSY | RESPIRATORY SYSTEM | PROGNOSTIC-SIGNIFICANCE | IDIOPATHIC PULMONARY-FIBROSIS | CLINICAL-SIGNIFICANCE | CRITICAL CARE MEDICINE | Biopsy - methods | Lung Diseases, Interstitial - pathology | Humans | Middle Aged | Bronchoscopy - methods | Idiopathic Pulmonary Fibrosis - diagnostic imaging | Male | Tomography, X-Ray Computed | Forced Expiratory Volume | Alveolitis, Extrinsic Allergic - physiopathology | Lung Diseases, Interstitial - diagnostic imaging | Alveolitis, Extrinsic Allergic - pathology | Adult | Female | Retrospective Studies | Lung Diseases, Interstitial - physiopathology | Bronchiolitis - physiopathology | Lung - pathology | Bronchiolitis - pathology | Lung - physiopathology | Vital Capacity | Pulmonary Diffusing Capacity | Bronchiolitis - diagnostic imaging | Alveolitis, Extrinsic Allergic - diagnostic imaging | Cryptogenic Organizing Pneumonia - diagnostic imaging | Idiopathic Pulmonary Fibrosis - pathology | Aged | Cryptogenic Organizing Pneumonia - physiopathology | Idiopathic Pulmonary Fibrosis - physiopathology | Lung - surgery | Cryptogenic Organizing Pneumonia - pathology | Cohort Studies | Bronchoscopy | Lung diseases, Interstitial | Lungs | Biopsy | Patient outcomes | Diagnosis | Research | Comparative analysis | Index Medicus | Abridged Index Medicus | UIP, usual interstitial pneumonia | DIP, desquamative interstitial pneumonia | Original Research | ILD, interstitial lung disease | SLB, surgical lung biopsy | IIP, idiopathic interstitial pneumonia | TBB, transbronchial biopsy | HRCT, high-resolution CT | IPF, idiopathic pulmonary fibrosis | NSIP, nonspecific interstitial pneumonia | HP, hypersensitivity pneumonitis | Diffuse Lung Disease
Journal Article
Annals of the Rheumatic Diseases, ISSN 0003-4967, 06/2015, Volume 74, Issue 6, pp. 1188 - 1194
Journal Article