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Journal Article
European Respiratory Journal, ISSN 0903-1936, 10/2015, Volume 46, Issue 4, pp. 976 - 987
Journal Article
Journal Article
CLINICS IN CHEST MEDICINE, ISSN 0272-5231, 09/2019, Volume 40, Issue 3, pp. 609 - 609
The European Respiratory Society/American Thoracic Society Task Force on Undifferentiated Forms of Connective Tissue Disease-associated Interstitial Lung... 
SURVIVAL | DIAGNOSIS | CALL | SERIES | Connective tissue diseases | CONNECTIVE-TISSUE DISEASE | Interstitial lung disease | Pulmonary fibrosis | RESPIRATORY SYSTEM | PREDICTORS | LUNG-DISEASE | IDIOPATHIC PULMONARY-FIBROSIS | Idiopathic interstitial pneumonias
Journal Article
American Journal of Respiratory and Critical Care Medicine, ISSN 1073-449X, 09/2013, Volume 188, Issue 6, pp. 733 - 748
Journal Article
American Journal of Respiratory and Critical Care Medicine, ISSN 1073-449X, 03/2015, Volume 191, Issue 6, pp. 646 - 655
Journal Article
European Respiratory Journal, ISSN 0903-1936, 03/2012, Volume 39, Issue 3, pp. 661 - 668
Journal Article
American journal of respiratory and critical care medicine, ISSN 1073-449X, 2014, Volume 190, Issue 2, pp. 208 - 217
Journal Article
American Journal of Respiratory and Critical Care Medicine, ISSN 1073-449X, 10/2007, Volume 176, Issue 7, pp. 691 - 697
Journal Article
American Journal of Respiratory and Critical Care Medicine, ISSN 1073-449X, 02/2008, Volume 177, Issue 4, pp. 433 - 439
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 | 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
Chest, ISSN 0012-3692, 07/2007, Volume 132, Issue 1, pp. 214 - 220
Journal Article