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Fibrotic Hypersensitivity Pneumonitis: Key Issues in Diagnosis and Management.
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- Journal of Clinical Medicine, 2017, v. 6, n. 6, p. 62, doi. 10.3390/jcm6060062
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- Article
Let's get physical.
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- Respirology, 2024, v. 29, n. 9, p. 841, doi. 10.1111/resp.14790
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- Article
Serum C‐reactive protein is associated with earlier mortality across different interstitial lung diseases.
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- Respirology, 2024, v. 29, n. 3, p. 228, doi. 10.1111/resp.14609
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- Publication type:
- Article
Education, education, education!
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- Respirology, 2024, v. 29, n. 2, p. 183, doi. 10.1111/resp.14649
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- Article
The power of music.
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- Respirology, 2023, v. 28, n. 8, p. 800, doi. 10.1111/resp.14538
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- Article
MUC5B rs35705950 minor allele associates with older age and better survival in idiopathic pulmonary fibrosis.
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- Respirology, 2023, v. 28, n. 5, p. 455, doi. 10.1111/resp.14440
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- Article
Home sweet home... or is it?
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- Respirology, 2023, v. 28, n. 4, p. 401, doi. 10.1111/resp.14476
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- Article
Phosphodiesterase 5 inhibitor treatment and survival in interstitial lung disease pulmonary hypertension: A Bayesian retrospective observational cohort study.
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- Respirology, 2023, v. 28, n. 3, p. 262, doi. 10.1111/resp.14378
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- Publication type:
- Article
Genetic testing in interstitial lung disease: An international survey.
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- Respirology, 2022, v. 27, n. 9, p. 747, doi. 10.1111/resp.14303
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- Article
Short‐term lung function changes predict mortality in patients with fibrotic hypersensitivity pneumonitis.
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- Respirology, 2022, v. 27, n. 3, p. 202, doi. 10.1111/resp.14204
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- Article
Pulmonary fibrosis associated with telomere‐related gene mutations: A complex inheritance.
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- Respirology, 2021, v. 26, n. 12, p. 1098, doi. 10.1111/resp.14168
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- Article
Serum markers of pulmonary epithelial damage in systemic sclerosis‐associated interstitial lung disease and disease progression.
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- Respirology, 2021, v. 26, n. 5, p. 461, doi. 10.1111/resp.13988
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- Article
Clinical trial design for acute exacerbations in idiopathic pulmonary fibrosis: A thorny path.
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- Respirology, 2019, v. 24, n. 7, p. 620, doi. 10.1111/resp.13584
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- Article
Pulmonary fibrosis: Genetic analysis of telomere‐related genes, telomere length measurement‐or both?
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- Respirology, 2019, v. 24, n. 2, p. 97, doi. 10.1111/resp.13456
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- Publication type:
- Article
Pulmonary hypertension in interstitial lung disease: Limitations of echocardiography compared to cardiac catheterization.
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- Respirology, 2018, v. 23, n. 7, p. 687, doi. 10.1111/resp.13250
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- Publication type:
- Article
Likelihood of pulmonary hypertension in patients with idiopathic pulmonary fibrosis and emphysema.
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- Respirology, 2018, v. 23, n. 6, p. 593, doi. 10.1111/resp.13231
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- Publication type:
- Article
Year in review 2017: Interstitial lung disease, pulmonary vascular disease and sleep.
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- Respirology, 2018, v. 23, n. 4, p. 421, doi. 10.1111/resp.13273
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- Publication type:
- Article
Patient-reported outcome measures in idiopathic pulmonary fibrosis: Where do we stand?
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- 2017
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- Publication type:
- Editorial
Rituximab in severe, treatment-refractory interstitial lung disease.
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- Respirology, 2014, v. 19, n. 3, p. 353, doi. 10.1111/resp.12214
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- Publication type:
- Article
Pulmonary function vascular index predicts prognosis in idiopathic interstitial pneumonia.
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- Respirology, 2012, v. 17, n. 4, p. 674, doi. 10.1111/j.1440-1843.2011.02121.x
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- Article
Brief report: Allergological evaluation of children with autism.
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- Journal of Autism & Developmental Disorders, 1995, v. 25, n. 3, p. 327
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- Article
Molecular Biomarkers in Interstitial Lung Diseases.
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- Molecular Diagnosis & Therapy, 2014, v. 18, n. 5, p. 505, doi. 10.1007/s40291-014-0109-0
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- Publication type:
- Article
Endothelin in Pulmonary Fibrosis.
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- American Journal of Respiratory Cell & Molecular Biology, 2011, v. 44, n. 1, p. 1, doi. 10.1165/rcmb.2009-0388TR
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- Publication type:
- Article
Combination of BAL and Computed Tomography Differentiates Progressive and Non-progressive Fibrotic Lung Diseases.
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- American Journal of Respiratory & Critical Care Medicine, 2023, v. 208, n. 9, p. 975, doi. 10.1164/rccm.202305-0796OC
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- Publication type:
- Article
Validation of Proposed Criteria for Progressive Pulmonary Fibrosis.
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- American Journal of Respiratory & Critical Care Medicine, 2023, v. 207, n. 1, p. 69, doi. 10.1164/rccm.202201-0124OC
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- Publication type:
- Article
The Burden and Impact of Cough in Patients with Idiopathic Pulmonary Fibrosis: An Analysis of the Prospective Observational PROFILE Study.
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- Annals of the American Thoracic Society, 2023, v. 20, n. 9, p. 1267, doi. 10.1513/AnnalsATS.202302-174OC
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- Article
Pleuroparenchymal Fibroelastosis. A Review of Clinical, Radiological, and Pathological Characteristics.
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- 2019
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- Publication type:
- journal article
Interleukin-31 promotes pathogenic mechanisms underlying skin and lung fibrosis in scleroderma.
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- Rheumatology, 2020, v. 59, n. 9, p. 2625, doi. 10.1093/rheumatology/keaa195
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- Publication type:
- Article
Circulating Biomarkers of Interstitial Lung Disease in Systemic Sclerosis.
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- International Journal of Rheumatology, 2012, p. 1, doi. 10.1155/2012/121439
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- Publication type:
- Article
Morphometric analysis of intralobular, interlobular and pleural lymphatics in normal human lung.
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- Journal of Anatomy, 2012, v. 220, n. 4, p. 396, doi. 10.1111/j.1469-7580.2011.01473.x
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- Publication type:
- Article
Diffuse alveolar haemorrhage associated with subsequent development of ANCA positivity and emphysema in three young adults.
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- 2019
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- Publication type:
- journal article
Antacid Therapy and Disease Progression in Patients with Idiopathic Pulmonary Fibrosis Who Received Pirfenidone.
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- Respiration, 2017, v. 93, n. 6, p. 415, doi. 10.1159/000468546
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- Publication type:
- Article
Respiratory Muscle Fatigue following Exercise in Patients with Interstitial Lung Disease.
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- Respiration, 2013, v. 85, n. 3, p. 220, doi. 10.1159/000338787
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- Publication type:
- Article
Short-Term Pulmonary Function Trends Are Predictive of Mortality in Interstitial Lung Disease Associated With Systemic Sclerosis.
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- Arthritis & Rheumatology, 2017, v. 69, n. 8, p. 1670, doi. 10.1002/art.40130
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- Publication type:
- Article
Microarray profiling reveals suppressed interferon stimulated gene program in fibroblasts from scleroderma-associated interstitial lung disease.
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- Respiratory Research, 2013, v. 14, n. 8, p. 1, doi. 10.1186/1465-9921-14-80
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- Publication type:
- Article
Microarray profiling reveals suppressed interferon stimulated gene program in fibroblasts from scleroderma-associated interstitial lung disease.
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- 2013
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- Publication type:
- journal article
Gene expression profiling reveals novel TGFβ targets in adult lung fibroblasts.
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- Respiratory Research, 2004, v. 5, p. 24, doi. 10.1186/1465-9921-5-24
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- Publication type:
- Article
Bromodomain and Extraterminal (BET) Protein Inhibition Restores Redox Balance and Inhibits Myofibroblast Activation.
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- BioMed Research International, 2019, p. 1, doi. 10.1155/2019/1484736
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- Publication type:
- Article
Correction to: A Closer Look at the Role of Anti-CCP Antibodies in the Pathogenesis of Rheumatoid Arthritis Associated Interstitial Lung Disease and Bronchiectasis.
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- 2021
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- Correction Notice
A Closer Look at the Role of Anti-CCP Antibodies in the Pathogenesis of Rheumatoid Arthritis-Associated Interstitial Lung Disease and Bronchiectasis.
- Published in:
- Rheumatology & Therapy, 2021, v. 8, n. 4, p. 1463, doi. 10.1007/s40744-021-00362-4
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- Publication type:
- Article
Review Series: Aspects of Interstitial lung disease: Connective tissue disease-associated interstitial lung disease: How does it differ from IPF? How should the clinical approach differ?
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- Chronic Respiratory Disease, 2011, v. 8, n. 1, p. 53, doi. 10.1177/1479972310393758
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- Publication type:
- Article
CYFRA 21-1 Predicts Progression in Idiopathic Pulmonary Fibrosis: A Prospective Longitudinal Analysis of the PROFILE Cohort.
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- 2022
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- Publication type:
- journal article
The Respiratory Microbiome in Chronic Hypersensitivity Pneumonitis Is Distinct from That of Idiopathic Pulmonary Fibrosis.
- Published in:
- 2021
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- Publication type:
- journal article
The Respiratory Microbiome in Chronic Hypersensitivity Pneumonitis is Distinct from that of Idiopathic Pulmonary Fibrosis.
- Published in:
- American Journal of Respiratory & Critical Care Medicine, 2021, v. 203, n. 3, p. E1, doi. 10.1164/rccm.202002-0460oc
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- Publication type:
- Article
BAL Is Safe and Well Tolerated in Individuals with Idiopathic Pulmonary Fibrosis: An Analysis of the PROFILE Study.
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- 2021
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- Publication type:
- letter
Home Oxygen Therapy for Adults with Chronic Lung Disease. An Official American Thoracic Society Clinical Practice Guideline.
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- 2020
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- Publication type:
- journal article
Etiology, Risk Factors, and Biomarkers in Systemic Sclerosis with Interstitial Lung Disease.
- Published in:
- 2020
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- Publication type:
- journal article
Comprehensive Supportive Care for Patients with Fibrosing Interstitial Lung Disease.
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- 2019
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- Publication type:
- journal article
Predicting Outcomes in Idiopathic Pulmonary Fibrosis Using Automated Computed Tomographic Analysis.
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- 2018
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- Publication type:
- journal article
Host-Microbial Interactions in Idiopathic Pulmonary Fibrosis.
- Published in:
- 2017
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- Publication type:
- journal article