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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
Chest, ISSN 0012-3692, 06/2016, Volume 149, Issue 6, pp. 1473 - 1481
Journal Article
European Respiratory Journal, ISSN 0903-1936, 08/2014, Volume 44, Issue 2, pp. 287 - 288
Journal Article
Journal Article
Archives of Pathology and Laboratory Medicine, ISSN 0003-9985, 03/2016, Volume 140, Issue 3, pp. 221 - 229
Context.-Three distinct patterns of pulmonary fibrosis, including usual interstitial pneumonia, fibrotic nonspecific interstitial pneumonia, and... 
SURVIVAL | MEDICINE, RESEARCH & EXPERIMENTAL | LUNG | DIAGNOSIS | ETIOLOGY | PROGNOSIS | CHRONIC HYPERSENSITIVITY PNEUMONITIS | GUIDELINES | PATHOLOGY | NONSPECIFIC INTERSTITIAL PNEUMONIA | PATTERN | DISEASE | MEDICAL LABORATORY TECHNOLOGY | Idiopathic Pulmonary Fibrosis - therapy | Alveolitis, Extrinsic Allergic - therapy | Prognosis | Lung Diseases, Interstitial - pathology | Humans | Lung - diagnostic imaging | Alveolitis, Extrinsic Allergic - diagnosis | Respiratory Mucosa - pathology | Alveolitis, Extrinsic Allergic - physiopathology | Alveolitis, Extrinsic Allergic - pathology | Lung Diseases, Interstitial - diagnosis | Lung Diseases, Interstitial - therapy | Pulmonary Fibrosis - diagnostic imaging | Lung Diseases, Interstitial - physiopathology | Pulmonary Fibrosis - etiology | Connective Tissue Diseases - physiopathology | Diagnosis, Differential | Lung - pathology | Connective Tissue Diseases - diagnosis | Terminology as Topic | Connective Tissue Diseases - therapy | Radiography | Idiopathic Pulmonary Fibrosis - diagnosis | Pulmonary Fibrosis - classification | Biopsy | Connective Tissue Diseases - pathology | Pulmonary Fibrosis - prevention & control | Idiopathic Pulmonary Fibrosis - pathology | Idiopathic Pulmonary Fibrosis - physiopathology | Respiratory Mucosa - diagnostic imaging | Development and progression | Pneumonia | Pulmonary fibrosis | Diagnosis | Bacterial pneumonia
Journal Article
Respiratory Medicine, ISSN 0954-6111, 05/2018, Volume 138, pp. 95 - 101
Pleuroparenchymal fibroelastosis (PPFE) has been described in hypersensitivity pneumonitis (HP) yet its functional implications are unclear. Combined pulmonary... 
Hypersensitivity pneumonia | Radiology thoracic | Interstitial lung disease | Pleuroparenchymal fibroelastosis | Emphysema | SURVIVAL | CARDIAC & CARDIOVASCULAR SYSTEMS | COMPUTED-TOMOGRAPHY | FEATURES | ENTITY | RESPIRATORY SYSTEM | LUNG-DISEASE | IDIOPATHIC PULMONARY-FIBROSIS | Prevalence | Prognosis | Humans | Middle Aged | Male | Tomography, X-Ray Computed | Alveolitis, Extrinsic Allergic - physiopathology | Fibrosis - epidemiology | Aged, 80 and over | Adult | Female | Pulmonary Emphysema - physiopathology | Fibrosis - physiopathology | Forced Expiratory Volume - physiology | Pulmonary Emphysema - diagnostic imaging | Pleura - diagnostic imaging | Elastic Tissue - pathology | Fibrosis - diagnostic imaging | Smoking - epidemiology | Alveolitis, Extrinsic Allergic - diagnostic imaging | Alveolitis, Extrinsic Allergic - epidemiology | Vital Capacity - physiology | Pleura - pathology | Aged | London - epidemiology | Pulmonary Emphysema - epidemiology | Respiratory Function Tests | Pneumonia | Hypersensitivity pneumonitis | Epidemiology | Emphysema, Pulmonary | Bacterial pneumonia | Respiratory function | Identification methods | Gender | Confidence intervals | Variables | Physiology | Standard deviation | Carbon monoxide | Alveolitis | Age | Phenotypes | Preservation | Pulmonary arteries | Mortality | Lung diseases | Hypersensitivity | Patients | Pneumonitis | Pulmonary fibrosis | Cysts | Rheumatoid arthritis | Fibrosis | Microvasculature | Smoking
Journal Article
Chest, ISSN 0012-3692, 2016, Volume 151, Issue 3, pp. 619 - 625
Background The treatment of chronic hypersensitivity pneumonitis (cHP) often includes systemic oral corticosteroids, but the optimal pharmacologic management... 
Pulmonary/Respiratory | azathioprine | mycophenolate mofetil | hypersensitivity pneumonitis | interstitial lung disease | SURVIVAL | LUNG | DIAGNOSIS | CYCLOPHOSPHAMIDE | GUIDELINES | RECOVERY | RESPIRATORY SYSTEM | RITUXIMAB | IDIOPATHIC PULMONARY-FIBROSIS | CORTICOSTEROID TREATMENT | CRITICAL CARE MEDICINE | Azathioprine - therapeutic use | Glucocorticoids - therapeutic use | Carbon Monoxide | Humans | Immunosuppressive Agents - therapeutic use | Middle Aged | Alveolitis, Extrinsic Allergic - drug therapy | Linear Models | Male | Treatment Outcome | Alveolitis, Extrinsic Allergic - physiopathology | Vital Capacity | Pulmonary Diffusing Capacity | Mycophenolic Acid - therapeutic use | Female | Aged | Retrospective Studies | Chronic Disease | Prednisone - therapeutic use | Care and treatment | Pharmacology, Experimental | Hypersensitivity pneumonitis | Lung diseases | Prednisone | Dosage and administration | Research | Mycophenolate mofetil | Azathioprine | Morbidity | MMF, mycophenolate mofetil | UBC, University of British Columbia | Dlco, diffusion capacity of the lung for carbon monoxide | ILD, interstitial lung disease | PFT, pulmonary function test | AZA, azathioprine | LMM, linear mixed-effects model | UCSF, University of California, San Francisco | UCalgary, University of Calgary | cHP, chronic hypersensitivity pneumonitis | HP, hypersensitivity pneumonitis | Diffuse Lung Disease
Journal Article
European Radiology, ISSN 0938-7994, 9/2017, Volume 27, Issue 9, pp. 3635 - 3646
Journal Article
Respirology, ISSN 1323-7799, 11/2017, Volume 22, Issue 8, pp. 1592 - 1597
Journal Article
Respiratory Medicine, ISSN 0954-6111, 08/2017, Volume 129, pp. 173 - 178
Journal Article