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2007, Lung biology in health and disease, ISBN 0849337151, Volume 220, xxviii, 697
Compiled by an international group of more than 40 authors, this reference book supplies an engaging and comprehensive review of the major topics and key... 
Hypersomnia | Narcolepsy | Hypersomnolence, Idiopathic | Kleine-Levin Syndrome | Neurology | Sleep Medicine | Pulmonary Medicine
Book
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
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
Journal Article
Parkinsonism & related disorders, ISSN 1353-8020, 1995
Journal
2015, ISBN 1107104726, xi, 287
"Puberty has long been recognised as a difficult and upsetting process for individuals and families, but it is now also being widely described as in crisis.... 
Puberty | Puberty, Precocious | Persönlichkeitsentwicklung | Hormones, Sex | Pubertät | Social aspects | Precocious puberty
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
American journal of respiratory and critical care medicine, ISSN 1073-449X, 10/2014, Volume 190, Issue 8, pp. 906 - 913
Journal Article
Chest, ISSN 0012-3692, 05/2016, Volume 149, Issue 5, pp. 1205 - 1214
BACKGROUND: Acute respiratory worsening (ARW) requiring hospitalization in patients with fibrotic interstitial lung disease (f-ILD) is common. Little is known... 
Fibrotic interstitial lung disease | Hospitalization | Acute respiratory decline | hospitalization | RESPIRATORY SYSTEM | acute respiratory decline | fibrotic interstitial lung disease | CLINICAL-FEATURES | IDIOPATHIC PULMONARY-FIBROSIS | PNEUMONIA | ACUTE EXACERBATION | CRITICAL CARE MEDICINE | Lung Diseases, Interstitial - etiology | Idiopathic Pulmonary Fibrosis - therapy | Respiration, Artificial - utilization | Idiopathic Interstitial Pneumonias - therapy | Humans | Middle Aged | Male | Forced Expiratory Volume | Hypercapnia | Lung Diseases, Interstitial - mortality | Lung Diseases, Interstitial - therapy | Idiopathic Interstitial Pneumonias - physiopathology | Aged, 80 and over | Adult | Female | Retrospective Studies | Lung Diseases, Interstitial - physiopathology | Length of Stay - statistics & numerical data | Respiratory Insufficiency - physiopathology | Acute Disease | Hospital Mortality | Respiratory Insufficiency - mortality | Risk Factors | Total Lung Capacity | Idiopathic Interstitial Pneumonias - mortality | Respiratory Insufficiency - therapy | Disease Progression | Vital Capacity | Pulmonary Diffusing Capacity | Idiopathic Pulmonary Fibrosis - mortality | Hypoxia | Aged | Idiopathic Pulmonary Fibrosis - physiopathology | Connective Tissue Diseases - complications | Cohort Studies | Acute respiratory distress syndrome | Care and treatment | Diagnosis | Research | Lung diseases | Risk factors
Journal Article
American Journal of Respiratory and Critical Care Medicine, ISSN 1073-449X, 09/2018, Volume 198, Issue 5, pp. e44 - e68
Journal Article
European Respiratory Journal, ISSN 0903-1936, 10/2015, Volume 46, Issue 4, pp. 976 - 987
Journal Article
Journal Article
American Journal of Respiratory and Critical Care Medicine, ISSN 1073-449X, 09/2013, Volume 188, Issue 6, pp. 733 - 748
Journal Article