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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
American Journal of Respiratory and Critical Care Medicine, ISSN 1073-449X, 09/2013, Volume 188, Issue 6, pp. 733 - 748
Journal Article
2017, ISBN 0323480241, 203
Clinically focused and designed to provide a to-the-point overview, Interstitial Lung Disease, by Drs. Talmadge King, Harold Collard, and Luca Richeldi, bring... 
Interstitial lung diseases
eBook
2008, Lung biology in health and disease, ISBN 9781420053425, Volume 227., xxv, 844 p., [16] p. of plates
Removing the guesswork associated with Interstitial Lung Disorders (ILDs) and bronchiolar disorders, Interstitial Pulmonary and Bronchiolar Disorders addresses... 
Bronchial Diseases | Lung Diseases, Interstitial | Bronchioles | Interstitial lung diseases | Diseases | Pulmonary Medicine
Book
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 | 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
Journal Article
European Respiratory Journal, ISSN 0903-1936, 10/2015, Volume 46, Issue 4, pp. 976 - 987
Journal Article
Respiratory Medicine, ISSN 0954-6111, 2016, Volume 119, pp. 150 - 154
Abstract Objective To describe the clinical phenotype and natural history of a cohort of patients with interstitial pneumonia with autoimmune features (IPAF).... 
Pulmonary/Respiratory | Connective tissue disease | Idiopathic interstitial pneumonia | Interstitial lung disease | Interstitial pneumonia with autoimmune features | CARDIAC & CARDIOVASCULAR SYSTEMS | RESPIRATORY SYSTEM | LUNG-DISEASE | CONNECTIVE-TISSUE DISEASE | SOCIETY | Amino Acyl-tRNA Synthetases - immunology | Lung Diseases, Interstitial - pathology | Humans | Immunosuppressive Agents - therapeutic use | Middle Aged | Idiopathic Interstitial Pneumonias - diagnosis | Male | Tomography, X-Ray Computed | Lung - diagnostic imaging | Adrenal Cortex Hormones - therapeutic use | Carbon Monoxide - metabolism | Pulmonary Diffusing Capacity - physiology | Lung Diseases, Interstitial - diagnosis | Adult | Female | Retrospective Studies | Lung Diseases, Interstitial - physiopathology | Diagnosis, Differential | Lung - pathology | Antibodies, Antinuclear | Autoimmune Diseases - immunology | Respiratory Function Tests - methods | Connective Tissue Diseases - diagnosis | Lung - physiopathology | Autoimmune Diseases - diagnosis | Enzyme Inhibitors - therapeutic use | Lung Diseases, Interstitial - drug therapy | Phenotype | Mycophenolic Acid - therapeutic use | Biopsy | Connective Tissue Diseases - pathology | Idiopathic Interstitial Pneumonias - pathology | Vital Capacity - physiology | Amino Acyl-tRNA Synthetases - antagonists & inhibitors | Medical colleges | Pneumonia | Pulmonary fibrosis | Bacterial pneumonia | Task forces | Histopathology | Raynaud disease | Lung diseases | Classification | Medical records | Patients
Journal Article
American Journal of Surgical Pathology, ISSN 0147-5185, 01/2000, Volume 24, Issue 1, pp. 19 - 33
Nonspecific interstitial pneumonia (NSIP) has been proposed as a histologic subtype of idiopathic interstitial pneumonia with lung biopsy findings that are... 
Diffuse alveolar damage | Usual interstitial pneumonia | Idiopathic interstitial pneumonia | Acute interstitial pneumonia | Bronchiolitis obliterans organizing pneumonia | Idiopathic pulmonary fibrosis | Nonspecific interstitial pneumonia | Interstitial fibrosis | Cellular interstitial pneumonia | Cellular, fibrosing, desquamative interstitial pneumonia | bronchiolitis obliterans organizing pneumonia acute interstitial pneumonia | BRONCHIOLITIS | SURGERY | usual interstitial pneumonia | diffuse alveolar damage | PULMONARY FIBROSIS | ALVEOLITIS | HISTOLOGIC-FINDINGS | idiopathic pulmonary fibrosis | PATHOLOGY | HUMAN-IMMUNODEFICIENCY-VIRUS | nonspecific interstitial pneumonia | HIGH-RESOLUTION CT | idiopathic interstitial pneumonia | FEATURES | cellular, fibrosing, desquamative interstitial pneumonia | PNEUMOCYSTIS-CARINII | cellular interstitial pneumonia | interstitial fibrosis | CLINICAL RELEVANCE | LUNG-DISEASE | Pulmonary Fibrosis - diagnosis | Smoking - adverse effects | Pulmonary Fibrosis - mortality | Diagnosis, Differential | Lung - pathology | Age Factors | Lung Diseases, Interstitial - pathology | Humans | Middle Aged | Risk Factors | Male | Cryptogenic Organizing Pneumonia - mortality | Pulmonary Fibrosis - pathology | Cryptogenic Organizing Pneumonia - diagnosis | Lung Diseases, Interstitial - mortality | Lung Diseases, Interstitial - diagnosis | Time Factors | Biopsy | Survival Analysis | Adult | Female | Aged | Cryptogenic Organizing Pneumonia - pathology
Journal Article
Clinical Rheumatology, ISSN 0770-3198, 8/2018, Volume 37, Issue 8, pp. 2125 - 2132
To investigate the clinical features, risk factors and outcomes of patients with interstitial pneumonia with autoimmune features (IPAF). A total of 1429... 
Undifferentiated connective tissue disease | Medicine & Public Health | Idiopathic interstitial pneumonia | Outcome | Rheumatology | Risk factor | Interstitial pneumonia with autoimmune features | AMERICAN-COLLEGE | UCTD | RHEUMATOLOGY/EUROPEAN LEAGUE | CONNECTIVE-TISSUE DISEASE | RHEUMATOLOGY | NATURAL-HISTORY | CLASSIFICATION CRITERIA | Age Factors | Lung Diseases, Interstitial - pathology | Humans | Immunosuppressive Agents - therapeutic use | Middle Aged | Idiopathic Interstitial Pneumonias - blood | Male | Tomography, X-Ray Computed | Adrenal Cortex Hormones - therapeutic use | Idiopathic Interstitial Pneumonias - complications | Lung Diseases, Interstitial - blood | Female | Retrospective Studies | Autoimmune Diseases - pathology | Autoimmune Diseases - drug therapy | Risk Factors | Autoimmune Diseases - complications | Treatment Outcome | Lung Diseases, Interstitial - complications | Lung Diseases, Interstitial - drug therapy | Autoimmune Diseases - blood | Idiopathic Interstitial Pneumonias - drug therapy | Smoking - epidemiology | Connective Tissue Diseases - pathology | Idiopathic Interstitial Pneumonias - pathology | Sex Factors | Aged | Medical research | Pneumonia | Pulmonary fibrosis | Bacterial pneumonia | Patient outcomes | Medicine, Experimental | Risk factors | Computed tomography | Lung diseases | Fibrosis | Population studies | Interferon | Multivariate analysis | Health risk assessment | Survival | Smoking
Journal Article
Journal of Cellular and Molecular Medicine, ISSN 1582-1838, 04/2010, Volume 14, Issue 4, pp. 729 - 740
Journal Article