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idiopathic interstitial pneumonia (32) 32
humans (19) 19
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idiopathic pulmonary fibrosis (15) 15
respiratory system (15) 15
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idiopathic interstitial pneumonias (11) 11
index medicus (11) 11
nonspecific interstitial pneumonia (11) 11
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iip (9) 9
pneumonia (8) 8
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adult (7) 7
classification (7) 7
ipf (7) 7
pulmonary fibrosis (7) 7
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survival (7) 7
biopsy (6) 6
features (6) 6
pulmonary-fibrosis (6) 6
bacterial pneumonia (5) 5
diagnosis, differential (5) 5
interstitial lung disease (5) 5
lung - pathology (5) 5
retrospective studies (5) 5
risk factors (5) 5
tomography, x-ray computed (5) 5
usual interstitial pneumonia (5) 5
aged, 80 and over (4) 4
diagnosis (4) 4
idiopathic interstitial pneumonias - diagnosis (4) 4
lung cancer (4) 4
lung diseases (4) 4
lung diseases, interstitial - pathology (4) 4
lung-disease (4) 4
nsip (4) 4
prognosis (4) 4
research (4) 4
bronchoalveolar lavage (3) 3
bronchoscopy (3) 3
cardiac & cardiovascular systems (3) 3
care and treatment (3) 3
cryptogenic organizing pneumonia (3) 3
forced vital capacity (3) 3
idiopathic pulmonary fibrosis - diagnosis (3) 3
idiopathic pulmonary-fibrosis (3) 3
iips (3) 3
internal medicine (3) 3
interstitial pneumonia (3) 3
lung diseases, interstitial - classification (3) 3
lung-dominant connective tissue disease (3) 3
medicine, general & internal (3) 3
mortality (3) 3
pathogenesis (3) 3
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pulmonary fibrosis - diagnosis (3) 3
pulmonary fibrosis - physiopathology (3) 3
undifferentiated connective tissue disease (3) 3
abridged index medicus (2) 2
adrenal cortex hormones - therapeutic use (2) 2
article (2) 2
biomarkers (2) 2
biomarkers - blood (2) 2
bronchoalveolar lavage fluid - cytology (2) 2
chronic hypersensitivity pneumonitis (2) 2
chronic obstructive pulmonary disease (2) 2
classification of iips (2) 2
cohort studies (2) 2
connective tissue diseases - complications (2) 2
critical care medicine (2) 2
cryptogenic organizing pneumonia - diagnosis (2) 2
development and progression (2) 2
diffuse lung disease (2) 2
dip, desquamative interstitial pneumonia (2) 2
disease (2) 2
diseases of the respiratory system (2) 2
enzyme-linked immunosorbent assay (2) 2
exercise prescription (2) 2
familial interstitial pneumonia (2) 2
fip (2) 2
follow-up studies (2) 2
forced expiratory volume (2) 2
fvc (2) 2
genetic aspects (2) 2
genome-wide association (2) 2
health risk assessment (2) 2
high-resolution ct (2) 2
hrct, high-resolution ct (2) 2
idiopathic interstitial pneumonias - diagnostic imaging (2) 2
idiopathic interstitial pneumonias - physiopathology (2) 2
idiopathic pulmonary fibrosis - diagnostic imaging (2) 2
idiopathic pulmonary fibrosis - pathology (2) 2
iip, idiopathic interstitial pneumonia (2) 2
ild, interstitial lung disease (2) 2
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Journal of Thoracic Disease, ISSN 2072-1439, 2018, Volume 10, Issue 8, pp. 4724 - 4732
Background: Idiopathic interstitial pneumonia (IIP) can induce type II alveolar epithelial cell proliferation and pulmonary basement membrane damage and... 
Diagnostic test | Idiopathic interstitial pneumonia (IIP) | Serum KL-6 | BIOMARKERS | idiopathic interstitial pneumonia (IIP) | MANAGEMENT | SURFACTANT PROTEIN-A | RESPIRATORY SYSTEM | LUNG-DISEASES | RISK | diagnostic test | PULMONARY-FIBROSIS | ACUTE EXACERBATION | Original
Journal Article
International Journal of Tuberculosis and Lung Disease, ISSN 1027-3719, 07/2016, Volume 20, Issue 7, pp. 978 - 984
Journal Article
Respiratory Medicine, ISSN 0954-6111, 2015, Volume 109, Issue 3, pp. 389 - 396
Summary Background Kinder et al. proposed a broader definition of undifferentiated connective tissue disease (UCTD) and reported that the entity of nonspecific... 
Pulmonary/Respiratory | SLB – surgical lung biopsy | NSIP – nonspecific interstitial pneumonia | IPF – idiopathic pulmonary fibrosis | UCTD – undifferentiated connective tissue disease | IIPs – idiopathic interstitial pneumonias | IIPs | Idiopathic pulmonary fibrosis | Nonspecific interstitial pneumonia | NSIP | SLB | Uctd -undifferentiated connective tissue disease | Surgical lung biopsy | Idiopathic interstitial pneumonias | IPF | SURVIVAL | CARDIAC & CARDIOVASCULAR SYSTEMS | SLB - surgical lung biopsy | IIPs - idiopathic interstitial pneumonias | RESPIRATORY SYSTEM | PIRFENIDONE | UCTD - undifferentiated conneaive tissue disease | LUNG-DISEASE | CLASSIFICATION | PREVALENCE | IPF - idiopathic pulmonary fibrosis | NSIP - nonspecific interstitial pneumonia | Japan - epidemiology | Predictive Value of Tests | Spirometry | Diagnosis, Differential | Prevalence | Prospective Studies | Follow-Up Studies | Humans | Middle Aged | Risk Factors | Idiopathic Interstitial Pneumonias - diagnosis | Connective Tissue Diseases - diagnosis | Tomography, X-Ray Computed - methods | Male | Idiopathic Interstitial Pneumonias - mortality | Idiopathic Interstitial Pneumonias - etiology | Forced Expiratory Volume | Idiopathic Pulmonary Fibrosis - diagnosis | Biopsy | Idiopathic Interstitial Pneumonias - physiopathology | Sensitivity and Specificity | Female | Aged | Connective Tissue Diseases - complications | Medical colleges | Pneumonia | Bacterial pneumonia | Confidence intervals | Survival analysis | Histopathology | Lung diseases | Medical prognosis | Carbon monoxide | Autoimmune diseases | Patients
Journal Article
Arthritis Research and Therapy, ISSN 1478-6354, 01/2016, Volume 18, Issue 1, p. 20
Journal Article
Respiratory Medicine, ISSN 0954-6111, 2016, Volume 117, pp. 27 - 32
Abstract Background and objective We hypothesized that increased pulmonary vascular permeability may play a role in the pathogenesis of an acute exacerbation... 
Pulmonary/Respiratory | Acute lung injury/acute respiratory distress syndrome (ALI/ARDS) | Angiopoietin-2 | Acute exacerbation of idiopathic interstitial pneumonias (AE-IIPs) | OXIDATIVE STRESS | CARDIAC & CARDIOVASCULAR SYSTEMS | PERMEABILITY | TIE2 | ACUTE LUNG INJURY | RESPIRATORY-DISTRESS-SYNDROME | CIRCULATING ANGIOPOIETIN-2 | RESPIRATORY SYSTEM | IN-VIVO | CRITICALLY-ILL PATIENTS | PULMONARY-FIBROSIS | ENDOTHELIAL GROWTH-FACTOR | Respiratory Distress Syndrome, Adult - physiopathology | Humans | Middle Aged | Idiopathic Pulmonary Fibrosis - diagnostic imaging | Idiopathic Interstitial Pneumonias - blood | Male | Acute Lung Injury - blood | Capillary Permeability - genetics | Respiratory Distress Syndrome, Adult - blood | Idiopathic Interstitial Pneumonias - diagnostic imaging | Inflammation - metabolism | Idiopathic Interstitial Pneumonias - physiopathology | Aged, 80 and over | Adult | Female | Lung - metabolism | Retrospective Studies | Angiopoietin-2 - blood | Acute Lung Injury - physiopathology | Lung - pathology | Tomography Scanners, X-Ray Computed | Disease Progression | Survival Analysis | Idiopathic Pulmonary Fibrosis - pathology | Aged | Lung - blood supply | Care and treatment | Pneumonia | Permeability | College teachers | Bacterial pneumonia | Respiratory therapy | Proteins | Heart failure | Pulmonary fibrosis | Respiratory distress syndrome | Pathogenesis | Inflammation | Manuscripts
Journal Article
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
Rigakuryoho Kagaku, ISSN 1341-1667, 03/2015, Volume 30, Issue 1, pp. 135 - 139
Purpose: The purpose of this study was to investigate the effect of pulmonary physical therapy for a patient with cryptogenic organizing pneumonia (COP), a... 
Idiopathic interstitial pneumonias | Classification of IIPs | Exercise prescription
Journal Article
Respiratory Medicine, ISSN 0954-6111, 2016, Volume 117, pp. 40 - 47
Abstract Background The aim of this study was to evaluate the incidence and clinical features of patients who developed collagen vascular disease (CVD) after... 
Pulmonary/Respiratory | Connective tissue disease (CTD) | Collagen vascular disease (CVD) | Idiopathic interstitial pneumonias (IIPs) | Interstitial pneumonia with autoimmune features (IPAF) | Nonspecific interstitial pneumonia (NSIP) | DERMATOMYOSITIS | CARDIAC & CARDIOVASCULAR SYSTEMS | POLYMYOSITIS | SJOGRENS-SYNDROME | CLASSIFICATION | DISORDERS | CONNECTIVE-TISSUE DISEASE | FEATURES | REVISED CRITERIA | RESPIRATORY SYSTEM | LUNG-DISEASE | Vascular Diseases - pathology | Connective Tissue Diseases - epidemiology | Lung Diseases, Interstitial - pathology | Vascular Diseases - complications | Humans | Middle Aged | Male | Vascular Diseases - epidemiology | Idiopathic Interstitial Pneumonias - complications | Incidence | Idiopathic Interstitial Pneumonias - diagnostic imaging | Adult | Female | Retrospective Studies | Autoimmune Diseases - pathology | Dermatomyositis - pathology | Autoimmune Diseases - epidemiology | Lung - pathology | Sjogren's Syndrome - pathology | Tomography Scanners, X-Ray Computed | Lung Diseases, Interstitial - complications | Vascular Diseases - diagnostic imaging | Arthritis, Rheumatoid - pathology | Collagen - metabolism | Lung Diseases, Interstitial - immunology | Smoking - epidemiology | Connective Tissue Diseases - pathology | Idiopathic Interstitial Pneumonias - pathology | Aged | Connective Tissue Diseases - complications | Blood circulation disorders | Medical colleges | Pneumonia | Pulmonary fibrosis | Bacterial pneumonia | Collagen | Diagnosis | Lupus | Biopsy | Lung diseases | Rheumatoid arthritis | Medical prognosis | Tomography | Health risk assessment | Pharmaceutical industry | Patients
Journal Article
Journal of Evidence Based Medicine and Healthcare, ISSN 2349-2562, 01/2019, Volume 6, Issue 1, pp. 68 - 70
BACKGROUND Cryptogenic Organizing Pneumonia (COP) is one of the major idiopathic interstitial pneumonia (IIP) according to revised American Thoracic Society/... 
Idiopathic Interstitial Pneumonia (IIP) | Cryptogenic Organizing Pneumonia (COP)
Journal Article
Translational Research, ISSN 1931-5244, 2014, Volume 163, Issue 5, pp. 494 - 502
TERT and MUC5B polymorphisms have been associated consistently with idiopathic pulmonary fibrosis (IPF) in recent genomewide genetic studies. However, it... 
Internal Medicine | genomewide association study | ILD | familial interstitial pneumonia | FVC pre | GWAS | single nucleotide polymorphism | forced vital capacity | NSIP | odds ratio | SNP | TERT | human telomerase reverse transcriptase gene | interstitial lung disease | interstitial pneumonia | postbronchodilator FEV1 percent predicted | airflow obstruction | FVC post | Abbreviations | BMI | forced expiratory volume at 1 second | body mass index | human mucin 5B gene | idiopathic pulmonary fibrosis | FIP | MUC5B | nonspecific interstitial pneumonia | idiopathic interstitial pneumonia | prebronchodilator FEV1 percent predicted | IIP | FEV1 post | FVC | postbronchodilator FVC percent predicted | confidence interval | FEV1 | FEV1 pre | IPF | chronic obstructive pulmonary disease | COPD | prebronchodilator FVC percent predicted | MEDICINE, RESEARCH & EXPERIMENTAL | MEDICINE, GENERAL & INTERNAL | TELOMERASE | SUSCEPTIBILITY | PROMOTER POLYMORPHISM | MUTATIONS | MEDICAL LABORATORY TECHNOLOGY | IDIOPATHIC PULMONARY-FIBROSIS | AIRWAYS | VARIANT | GENOME-WIDE ASSOCIATION | Mucin-5B - metabolism | Genetic Predisposition to Disease | Telomerase - genetics | Lung Diseases, Interstitial - classification | Lung Diseases, Interstitial - genetics | Mucin-5B - genetics | Humans | Risk Factors | Genotype | Telomerase - metabolism | Polymorphism, Single Nucleotide | Odds Ratio | Genetic aspects | Telomerase | Lung diseases | Mucins | polymorphism
Journal Article