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1. Full Text Predicting survival across chronic interstitial lung disease: The ILD-GAP model
by Ryerson, Christopher J and Vittinghoff, Eric and Ley, Brett and Lee, Joyce S and Mooney, Joshua J and Jones, Kirk D and Elicker, Brett M and Wolters, Paul J and Koth, Laura L and King Jr, Talmadge E and Collard, Harold R
Chest, ISSN 0012-3692, 2014, Volume 145, Issue 4, pp. 723 - 728
Background: Risk prediction is challenging in chronic interstitial lung disease (ILD) because of heterogeneity in disease-specific and patient-specific... 
SYSTEM | DIAGNOSIS | STANDARDIZATION | HYPERSENSITIVITY PNEUMONITIS | RESPIRATORY SYSTEM | PREVALENCE | INDEX | IDIOPATHIC PULMONARY-FIBROSIS | CRITICAL CARE MEDICINE | Models, Theoretical | Prognosis | Humans | Middle Aged | Male | Survival Rate | Lung Diseases, Interstitial - complications | Lung Diseases, Interstitial - mortality | Alveolitis, Extrinsic Allergic - complications | Female | Aged | Idiopathic Pulmonary Fibrosis - complications | Chronic Disease | Connective Tissue Diseases - complications | Outcome and process assessment (Health Care) | Lung diseases, Interstitial | Usage | Models | Research | Patient outcomes
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2. Full Text Rheumatoid arthritis-interstitial lung disease-associated mortality
by Olson, Amy L and Swigris, Jeffrey J and Sprunger, David B and Fischer, Aryeh and Fernandez-Perez, Evans R and Solomon, Josh and Murphy, James and Cohen, Marc and Raghu, Ganesh and Brown, Kevin K
American Journal of Respiratory and Critical Care Medicine, ISSN 1073-449X, 02/2011, Volume 183, Issue 3, pp. 372 - 378
Rationale: Mortality rates from rheumatoid arthritis-associated interstitial lung disease (RA-ILD) are largely unknown. Objectives: We sought to determine... 
Prevalence | Interstitial lung disease | Epidemiology | Mortality rates | Rheumatoid arthritis | epidemiology | prevalence | interstitial lung disease | RESPIRATORY SYSTEM | DEATH | PNEUMONIA | rheumatoid arthritis | TRENDS | mortality rates | MANIFESTATIONS | CRITICAL CARE MEDICINE | United States - epidemiology | Age Factors | Humans | Middle Aged | Male | Lung Diseases, Interstitial - complications | Arthritis, Rheumatoid - complications | Cause of Death | Lung Diseases, Interstitial - mortality | Regression Analysis | Sex Factors | Aged, 80 and over | Female | Poisson Distribution | Aged | Arthritis, Rheumatoid - mortality | D. Interstitial Lung Disease
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3. Full Text Idiopathic Nonspecific Interstitial Pneumonia: Lung Manifestation of Undifferentiated Connective Tissue Disease?
by Kinder, Brent W and Collard, Harold R and Koth, Laura and Daikh, David I and Wolters, Paul J and Elicker, Brett and Jones, Kirk D and King, Talmadge E., Jr
American Journal of Respiratory and Critical Care Medicine, ISSN 1073-449X, 10/2007, Volume 176, Issue 7, pp. 691 - 697
Rationale: The American Thoracic Society/European Respiratory Society International Consensus Classification panel identified the clinical entity idiopathic... 
Autoimmune disease | Collagen vascular | Undifferentiated connective tissue | Idiopathic interstitial pneumonia | Systemic rheumatic disease | ANTINUCLEAR ANTIBODY | HISTOPATHOLOGIC SUBSETS | systemic rheumatic disease | SYSTEMIC-SCLEROSIS | autoimmune disease | idiopathic interstitial pneumonia | CLINICAL ENTITY | AUTOIMMUNE PANCREATITIS | RESPIRATORY SYSTEM | undifferentiated connective tissue | UCTD | PROGNOSTIC-SIGNIFICANCE | CRYPTOGENIC FIBROSING ALVEOLITIS | HISTOLOGIC PATTERN | collagen vascular | PULMONARY-FIBROSIS | CRITICAL CARE MEDICINE | Lung - pathology | Lung Diseases, Interstitial - pathology | Humans | Middle Aged | Connective Tissue Diseases - diagnosis | Male | Tomography, X-Ray Computed | Lung - diagnostic imaging | Autoimmune Diseases - diagnosis | Lung Diseases, Interstitial - complications | Lung Diseases, Interstitial - diagnostic imaging | Lung Diseases, Interstitial - diagnosis | Connective Tissue Diseases - pathology | Aged, 80 and over | Adult | Female | Aged | Connective Tissue Diseases - diagnostic imaging | Autoimmune Diseases - pathology | Connective Tissue Diseases - complications | C. Interstitial Lung Disease
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4. Full Text Incidence and complications of interstitial lung disease in users of tocilizumab, rituximab, abatacept and anti-tumor necrosis factor aα agents, a retrospective cohort study
by Curtis, Jeffrey R and Sarsour, Khaled and Napalkov, Pavel and Costa, Laurie A and Schulman, Kathy L
Arthritis Research and Therapy, ISSN 1478-6354, 11/2015, Volume 17, Issue 1, p. 319
Interstitial lung disease (ILD) is a common extra-articular condition in rheumatoid arthritis (RA), but few studies have systematically investigated its... 
Hospitalization | Interstitial lung disease | Biologics | Rheumatoid arthritis | Antibodies, Monoclonal, Humanized - therapeutic use | Humans | Middle Aged | Male | Lung Diseases, Interstitial - complications | Arthritis, Rheumatoid - complications | Incidence | Rituximab - therapeutic use | Arthritis, Rheumatoid - drug therapy | Abatacept - therapeutic use | Adult | Female | Aged | Retrospective Studies | Lung Diseases, Interstitial - epidemiology | Tumor Necrosis Factor-alpha - antagonists & inhibitors | Antirheumatic Agents - therapeutic use | Cohort Studies
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5. Full Text Pulmonary hypertension in interstitial lung disease
by Behr, J and Ryu, J. H
European Respiratory Journal, ISSN 0903-1936, 06/2008, Volume 31, Issue 6, pp. 1357 - 1367
In the lungs, parenchymal and vascular remodelling share pathomechanisms that may explain the relatively high prevalence (30-40%) of pulmonary hypertension... 
Connective tissue disease | Pulmonary fibrosis | Sarcoidosis | Interstitial lung disease | Pulmonary hypertension | BRAIN NATRIURETIC PEPTIDE | pulmonary hypertension | sarcoidosis | N-ACETYLCYSTEINE | SYSTEMIC-SCLEROSIS | TRICUSPID REGURGITATION | SOLUBLE GUANYLATE-CYCLASE | connective tissue disease | EPITHELIAL-MESENCHYMAL TRANSITION | CLINICAL-PRACTICE GUIDELINES | FIBROSING ALVEOLITIS | interstitial lung disease | RESPIRATORY SYSTEM | pulmonary fibrosis | ARTERIAL-HYPERTENSION | OF-THE-LITERATURE | Cardiac Catheterization | Hypertension, Pulmonary - diagnosis | Lung Transplantation | Echocardiography | Humans | Hypertension, Pulmonary - physiopathology | Biomarkers - blood | Lung Diseases, Interstitial - physiopathology | Lung Diseases, Interstitial - complications | Hypertension, Pulmonary - complications
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6. Full Text An integrated palliative and respiratory care service for patients with advanced disease and refractory breathlessness: a randomised controlled trial
by Higginson, Irene J, Prof and Bausewein, Claudia, Prof and Reilly, Charles C, PhD and Gao, Wei, PhD and Gysels, Marjolein, PhD and Dzingina, Mendwas, MSc and McCrone, Paul, Prof and Booth, Sara, MD and Jolley, Caroline J, PhD and Moxham, John, Prof
Lancet Respiratory Medicine, The, ISSN 2213-2600, 2014, Volume 2, Issue 12, pp. 979 - 987
Summary Background Breathlessness is a common and distressing symptom, which increases in many diseases as they progress and is difficult to manage. We... 
Pulmonary/Respiratory | OBSTRUCTIVE PULMONARY-DISEASE | ADVANCED CANCER | MANAGEMENT | RESPIRATORY SYSTEM | NEEDS | PROTOCOL | REHABILITATION | QUALITY-OF-LIFE | INTERVENTION | COPD | CRITICAL CARE MEDICINE | Single-Blind Method | Heart Failure - complications | Motor Neuron Disease - complications | Humans | Respiratory Therapy - methods | Treatment Outcome | Pulmonary Disease, Chronic Obstructive - complications | Lung Diseases, Interstitial - complications | Dyspnea - therapy | Quality of Life | Adult | Chronic Disease | Palliative Care - methods
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7. Full Text Shared genetic predisposition in rheumatoid arthritis-interstitial lung disease and familial pulmonary fibrosis
by Juge, Pierre-Antoine and Borie, Raphaël and Kannengiesser, Caroline and Gazal, Steven and Revy, Patrick and Wemeau-Stervinou, Lidwine and Debray, Marie-Pierre and Ottaviani, Sébastien and Marchand-Adam, Sylvain and Nathan, Nadia and Thabut, Gabriel and Richez, Christophe and Nunes, Hilario and Callebaut, Isabelle and Justet, Aurélien and Leulliot, Nicolas and Bonnefond, Amélie and Salgado, David and Richette, Pascal and Desvignes, Jean-Pierre and Lioté, Huguette and Froguel, Philippe and Allanore, Yannick and Sand, Olivier and Dromer, Claire and Flipo, René-Marc and Clément, Annick and Béroud, Christophe and Sibilia, Jean and Coustet, Baptiste and Cottin, Vincent and Boissier, Marie-Christophe and Wallaert, Benoit and Schaeverbeke, Thierry and Le Moal, Florence Dastot and Frazier, Aline and Ménard, Christelle and Soubrier, Martin and Saidenberg, Nathalie and Valeyre, Dominique and Amselem, Serge and Boileau, Catherine and Crestani, Bruno and Dieudé, Philippe and FREX Consortium and FREX consortium and the FREX consortium
European Respiratory Journal, ISSN 0903-1936, 05/2017, Volume 49, Issue 5, pp. 1602314 - 1602314
Despite its high prevalence and mortality, little is known about the pathogenesis of rheumatoid arthritis-associated interstitial lung disease (RA-ILD). Given... 
MORTALITY | RTEL1 | VARIANTS | PATTERN | TELOMERASE | RESPIRATORY SYSTEM | COHORT | DEATH | MUTATIONS | PNEUMONIA | IDENTIFICATION | Humans | Middle Aged | Male | Pulmonary Fibrosis - genetics | Arthritis, Rheumatoid - complications | Case-Control Studies | Exome | Telomerase - genetics | Adult | Female | DNA Helicases - genetics | Genetic Predisposition to Disease | Genetic Association Studies | Pulmonary Fibrosis - complications | Europe | Risk Factors | Lung Diseases, Interstitial - complications | Sequence Analysis, DNA | Arthritis, Rheumatoid - genetics | Phenotype | Lung Diseases, Interstitial - genetics | Heterozygote | Aged | Software | Mutation | Telomeres | Pulmonary fibrosis | Rheumatoid arthritis | Lung diseases | Fibrosis | Risk factors | Life Sciences | Human health and pathology
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8. Full Text Diffuse cystic lung disease: Part I
by Gupta, Nishant and Vassallo, Robert and Wikenheiser-Brokamp, Kathryn A and McCormack, Francis X
American Journal of Respiratory and Critical Care Medicine, ISSN 1073-449X, 06/2015, Volume 191, Issue 12, pp. 1354 - 1366
The diffuse cystic lung diseases (DCLDs) are a group of pathophysiologically heterogenous processes that are characterized by the presence of multiple... 
Lung cysts | Tuberous sclerosis | High-resolution computed tomography | Pulmonary Langerhans cell histiocytosis | Lymphangioleiomyomatosis | high-resolution computed tomography | LANGERHANS-CELL HISTIOCYTOSIS | PNEUMOCYSTIS-CARINII-PNEUMONIA | tuberous sclerosis | lung cysts | RECURRENT RESPIRATORY PAPILLOMATOSIS | TUBEROUS SCLEROSIS COMPLEX | DESQUAMATIVE INTERSTITIAL PNEUMONIA | RESPIRATORY SYSTEM | pulmonary Langerhans cell histiocytosis | THIN-SECTION CT | ERDHEIM-CHESTER-DISEASE | IDIOPATHIC PULMONARY-FIBROSIS | OF-THE-LITERATURE | lymphangioleiomyomatosis | ENDOMETRIAL STROMAL SARCOMA | CRITICAL CARE MEDICINE | Smoking - adverse effects | Neoplasms - complications | Lung - pathology | Lymphangioleiomyomatosis - complications | Humans | Lung Diseases, Interstitial - complications | Infection - complications | Lung Diseases - etiology | Histiocytosis, Langerhans-Cell - complications | Concise Clinical Review
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9. Full Text Polymyositis-Dermatomyositis-associated Interstitial Lung Disease
by DOUGLAS, WILLIAM W and TAZELAAR, HENRY D and HARTMAN, THOMAS E and HARTMAN, ROBERT P and DECKER, PAUL A and SCHROEDER, DARRELL R and RYU, JAY H
American Journal of Respiratory and Critical Care Medicine, ISSN 1073-449X, 10/2001, Volume 164, Issue 7, pp. 1182 - 1185
We report findings in 70 patients with both diffuse interstitial lung disease and either polymyositis (PM) or dermatomyositis (DM). Initial presentations were... 
Prednisone | Azathioprine | Interstitial lung disease | Survival | Polymyositis-dermatomyositis | IDIOPATHIC PULMONARY FIBROSIS | ALVEOLITIS | CYCLOPHOSPHAMIDE | survival | azathioprine | PNEUMONIA | CT | interstitial lung disease | RESPIRATORY SYSTEM | TERM FOLLOW-UP | PROGNOSTIC-SIGNIFICANCE | prednisone | HISTOLOGIC PATTERN | polymyositis-dermatomyositis | CRITICAL CARE MEDICINE | Polymyositis - drug therapy | Humans | Middle Aged | Male | Polymyositis - complications | Survival Rate | Dermatomyositis - mortality | Lung Diseases, Interstitial - complications | Dermatomyositis - complications | Lung Diseases, Interstitial - drug therapy | Lung Diseases, Interstitial - mortality | Dermatomyositis - drug therapy | Female | Retrospective Studies | Polymyositis - mortality
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10. Full Text Prognostic factors for myositis-associated interstitial lung disease
by Fujisawa, Tomoyuki and Hozumi, Hironao and Kono, Masato and Enomoto, Noriyuki and Hashimoto, Dai and Nakamura, Yutaro and Inui, Naoki and Yokomura, Koshi and Koshimizu, Naoki and Toyoshima, Mikio and Shirai, Toshihiro and Yasuda, Kazumasa and Hayakawa, Hiroshi and Suda, Takafumi
PLoS ONE, ISSN 1932-6203, 06/2014, Volume 9, Issue 6, p. e98824
Background: Interstitial lung disease (ILD) is a common manifestation of polymyositis (PM), dermatomyositis (DM), and clinically amyopathic dermatomyositis... 
GENE 5 | POLYMYOSITIS | MULTIDISCIPLINARY SCIENCES | IDIOPATHIC INFLAMMATORY MYOPATHIES | CLINICALLY AMYOPATHIC DERMATOMYOSITIS | SINE MYOSITIS | SPECTRUM | JAPANESE PATIENTS | SOCIETY | FEATURES | Prognosis | Lung Diseases, Interstitial - pathology | Clinical Laboratory Techniques | Humans | Middle Aged | Male | Tomography, X-Ray Computed | Myositis - complications | Lung Diseases, Interstitial - complications | Lung Diseases, Interstitial - diagnosis | Lung Diseases, Interstitial - therapy | Survival Analysis | Female | Aged | Retrospective Studies | Health aspects | Analysis | Mortality | Lung diseases | Immunosuppressive agents | Corticoids | Pneumonia | Arthritis | Dyspnea | Consolidation | Computed tomography | Bronchoalveolar lavage | Diagnosis | Alveoli | Age | Enzymes | Corticosteroids | Internal medicine | Dermatomyositis | Melanoma | Bronchus | Hazards | Leukocytes (neutrophilic) | Bronchiectasis | Patients | Survival | Fever | Cough | Medicine | Polymyositis | Hospitals | Pulmonary fibrosis | Statistical models | Medical prognosis | Myositis | Respiration
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11. Full Text Histopathologic Pattern and Clinical Features of Rheumatoid Arthritis-Associated Interstitial Lung Disease
by Lee, Hyun-Kyung and Kim, Dong Soon and Yoo, Bin and Seo, Joon Beom and Rho, Jae-Yoon and Colby, Thomas V and Kitaichi, Masanori
Chest, ISSN 0012-3692, 06/2005, Volume 127, Issue 6, pp. 2019 - 2027
To investigate the histopathologic pattern and clinical features of patients with rheumatoid arthritis (RA)-associated interstitial lung disease (ILD)... 
usual interstitial pneumonia | nonspecific interstitial pneumonia | prognosis | rheumatoid arthritis | surgical lung biopsy | bronchiolitis | Prognosis | Usual interstitial pneumonia | Surgical lung biopsy | Nonspecific interstitial pneumonia | Rheumatoid arthritis | Bronchiolitis | BRONCHITIS | ALVEOLITIS | BIOPSY | COLLAGEN VASCULAR-DISEASE | PNEUMONIA | DIAGNOSTIC-ACCURACY | RESPIRATORY SYSTEM | THIN-SECTION CT | IDIOPATHIC PULMONARY-FIBROSIS | Immunohistochemistry | Severity of Illness Index | Lung Diseases, Interstitial - pathology | Humans | Middle Aged | Bronchoalveolar Lavage | Probability | Male | Tomography, X-Ray Computed | Lung Diseases, Interstitial - complications | Arthritis, Rheumatoid - complications | Arthritis, Rheumatoid - pathology | Sensitivity and Specificity | Statistics, Nonparametric | Adult | Female | Aged | Retrospective Studies | Biopsy, Needle | Respiratory Function Tests | Cohort Studies | Care and treatment | Usage | Pulmonary fibrosis | Lungs | Biopsy
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12. Full Text IgG4-related lung disease presenting as interstitial lung disease with bronchiolitis A case report
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
Rationale: IgG4-related disease is a rare and novel disease entity that tends to involve multiple organs. The pulmonary manifestation of this disease is highly... 
MEDICINE, GENERAL & INTERNAL | IgG4 | PULMONARY MANIFESTATIONS | interstitial lung disease | bronchiolitis | Diagnosis, Differential | Lung Diseases - diagnosis | Humans | Immunosuppressive Agents - therapeutic use | Male | Lung Diseases - drug therapy | Lung Diseases, Interstitial - complications | Lung Diseases - immunology | Lung Diseases, Interstitial - diagnosis | Immunoglobulin G - immunology | Thoracic Surgery, Video-Assisted | Bronchiolitis - diagnosis | Adult | Bronchiolitis - complications | Lung Diseases - pathology | Respiratory Function Tests
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13. Full Text Pleuroparenchymal fibroelastosis: A spectrum of histopathological and imaging phenotypes
by Reddy, Taryn L and Tominaga, Masaki and Hansell, David M and Von Der Thusen, Jan and Rassl, Doris and Parfrey, Helen and Guy, Suzy and Twentyman, Orion and Rice, Alexandra and Maher, Toby M and Renzoni, Elisabetta A and Wells, Athol U and Nicholson, Andrew G
European Respiratory Journal, ISSN 0903-1936, 08/2012, Volume 40, Issue 2, pp. 377 - 385
Pleuroparenchymal fibroelastosis (PPFE) is a rare condition characterised by predominantly upper lobe pleural and subjacent parenchymal fibrosis, the latter... 
Infection | Interstitial lung disease | Lung | Pleuropulmonary fibroelastosis | lung | PULMONARY | FIBROSIS | ASPERGILLOSIS | interstitial lung disease | RESPIRATORY SYSTEM | pleuropulmonary fibroelastosis | Lung - pathology | Pulmonary Alveoli - pathology | Lung Diseases, Interstitial - pathology | Humans | Middle Aged | Tomography, X-Ray Computed - methods | Male | Treatment Outcome | Lung - diagnostic imaging | Pulmonary Fibrosis - pathology | Lung Diseases, Interstitial - complications | Pleura - diagnostic imaging | Cough | Lung Diseases, Interstitial - diagnostic imaging | Phenotype | Dyspnea | Biopsy | Pleura - pathology | Aged, 80 and over | Adult | Female | Aged
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14. Full Text Cyclophosphamide for connective tissue disease-associated interstitial lung disease
by Barnes, Hayley and Holland, Anne E and Westall, Glen P and Goh, Nicole S.L and Glaspole, Ian N
Cochrane Database of Systematic Reviews, ISSN 1469-493X, 01/2018, Volume 2018, Issue 1, pp. CD010908 - CD010908
Background Approximately one-third of individuals with interstitial lung disease (ILD) have associated connective tissue disease (CTD). The connective tissue... 
CONTROLLED-TRIAL | MEDICINE, GENERAL & INTERNAL | SCLERODERMA LUNG | RESOLUTION CT-SCAN | SYSTEMIC-SCLEROSIS PATIENTS | DOUBLE-BLIND | COLLAGEN VASCULAR-DISEASE | QUALITY-OF-LIFE | PULSE CYCLOPHOSPHAMIDE | MYCOPHENOLATE-MOFETIL | PULMONARY-FIBROSIS | Humans | Immunosuppressive Agents - therapeutic use | Lung Diseases, Interstitial - complications | Cyclophosphamide - adverse effects | Lung Diseases, Interstitial - drug therapy | Cyclophosphamide - therapeutic use | Randomized Controlled Trials as Topic | Vital Capacity - drug effects | Connective Tissue Diseases - drug therapy | Lung - drug effects | Scleroderma, Systemic | Quality of Life | Immunosuppressive Agents - adverse effects | Connective Tissue Diseases - complications | Index Medicus
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