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Sarcoidosis, vasculitis, and diffuse lung diseases, ISSN 1124-0490, 1996
Journal
American Journal of Respiratory and Critical Care Medicine, ISSN 1073-449X, 06/2008, Volume 177, Issue 12, pp. 1348 - 1357
Journal Article
Journal Article
Chest, ISSN 0012-3692, 08/2010, Volume 138, Issue 2, pp. 251 - 256
Journal Article
by Chen, CF and Chu, KA and Tseng, YC and Wu, CC and Lai, RS
MEDICINE, ISSN 0025-7974, 12/2017, Volume 96, Issue 49, p. e9140
.... The pulmonary manifestation of this disease is highly variable and may mimic lung cancer, pneumonia, interstitial lung disease (ILD... 
MEDICINE, GENERAL & INTERNAL | IgG4 | PULMONARY MANIFESTATIONS | interstitial lung disease | bronchiolitis
Journal Article
Cancer science, ISSN 1349-7006, 2019, Volume 110, Issue 12, pp. 3738 - 3745
Journal Article
Arthritis research & therapy, ISSN 1478-6362, 2015, Volume 17, Issue 1, p. 372
Journal Article
The New England journal of medicine, ISSN 1533-4406, 2019, Volume 380, Issue 26, pp. 2518 - 2528
Journal Article
Chest, ISSN 0012-3692, 04/2017, Volume 151, Issue 4, pp. 813 - 820
Background Cough is a common symptom of scleroderma-related interstitial lung disease (SSc-ILD... 
immunosuppressive therapy | health-related quality of life | interstitial lung disease | cough | scleroderma | TRIAL | RESPIRATORY SYSTEM | REFLEX | ORAL CYCLOPHOSPHAMIDE | QUESTIONNAIRE | VALIDITY | CRITICAL CARE MEDICINE | Severity of Illness Index | Cough - drug therapy | Humans | Immunosuppressive Agents - therapeutic use | Middle Aged | Male | Treatment Outcome | Lung Diseases, Interstitial - complications | Enzyme Inhibitors - therapeutic use | Lung Diseases, Interstitial - drug therapy | Cyclophosphamide - therapeutic use | Cough - etiology | Gastroesophageal Reflux - complications | Mycophenolic Acid - therapeutic use | Scleroderma, Systemic - complications | Quality of Life | Female | Respiratory Function Tests | Scleroderma, Systemic - drug therapy | Symptomatology | Chest | Care and treatment | Lung diseases, Interstitial | Systemic scleroderma | Analysis | Scleroderma (Disease) | Research | Risk factors | Cough | Quality of life | Diseases | MMF, mycophenolate mofetil | QILD, quantitative interstitial lung disease | Original Research | QLF, quantitative lung fibrosis | QoL, quality of life | GERD, gastroesophageal reflux disease | HRCT, high-resolution CT | TDI, transition dyspnea index | SSc-ILD, systemic sclerosis-related interstitial lung disease | BDI, baseline dyspnea index | RCT, randomized controlled trial | PPI, proton pump inhibitor | SLS, Scleroderma Lung Study | SGRQ, St. George’s Respiratory Questionnaire | ILD, interstitial lung disease | LM, lobe of maximal involvement | LCQ, Leicester Cough Questionnaire | SF-36, 36-item Short-Form Survey | Dlco, diffusing capacity of lung for carbon monoxide | VAS, visual analog scale | CYC, cyclophosphamide | WL, whole lung | FC, frequent cough | HAQ-DI, Health Assessment Questionnaire Disability Index | Signs and Symptoms of Chest Disease
Journal Article
Chest, ISSN 0012-3692, 07/2017, Volume 152, Issue 1, pp. 103 - 112
...), do not fit neatly into the category of connective tissue disease-associated interstitial lung disease (CTD-ILD... 
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
Journal Article
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