Keck School Faculty

Toby Maher

Toby Maher

Professor of Clinical Medicine
Medicine
IRD 720 2020 Zonal Avenue Health Sciences Campus los angeles

Idiopathic Pulmonary Fibrosis Is Associated with Common Genetic Variants and Limited Rare Variants Am J Respir Crit Care Med. 2023 May 01; 207(9):1194-1202. . View in PubMed

The causal relationship between gastro-esophageal reflux disease and idiopathic pulmonary fibrosis: A bidirectional two-sample Mendelian randomization study Eur Respir J. 2023 Apr 20. . View in PubMed

Knowledge gaps in fibrotic interstitial lung disease in pan-Asian populations: data not missing at random? Lancet Respir Med. 2023 Apr 04.. View in PubMed

Phosphodiesterase 4B inhibition: a potential novel strategy for treating pulmonary fibrosis Eur Respir Rev. 2023 Mar 31; 32(167). . View in PubMed

Change in gait speed and adverse outcomes in patients with idiopathic pulmonary fibrosis: A prospective cohort study Respirology. 2023 Mar 23. . View in PubMed

Weight loss and outcomes in subjects with progressive pulmonary fibrosis: data from the INBUILD trial Respir Res. 2023 Mar 09; 24(1):71. . View in PubMed

PCSK6 and Survival in Idiopathic Pulmonary Fibrosis Am J Respir Crit Care Med. 2023 Feb 13. . View in PubMed

MUC5B rs35705950 minor allele associates with older age and better survival in idiopathic pulmonary fibrosis Respirology. 2023 05; 28(5):455-464. . View in PubMed

GLPG1205 for idiopathic pulmonary fibrosis: a phase 2 randomised placebo-controlled trial Eur Respir J. 2023 03; 61(3). . View in PubMed

Effect of nintedanib in patients with systemic sclerosis-associated interstitial lung disease and risk factors for rapid progression RMD Open. 2023 02; 9(1). . View in PubMed

Rituximab versus intravenous cyclophosphamide in patients with connective tissue disease-associated interstitial lung disease in the UK (RECITAL): a double-blind, double-dummy, randomised, controlled, phase 2b trial Lancet Respir Med. 2023 01; 11(1):45-54. . View in PubMed

Home monitoring in interstitial lung diseases Lancet Respir Med. 2023 01; 11(1):97-110. . View in PubMed

Longitudinal lung function and gas transfer in individuals with idiopathic pulmonary fibrosis: a genome-wide association study Lancet Respir Med. 2023 01; 11(1):65-73. . View in PubMed

Impact of lung function and baseline clinical characteristics on patient-reported outcome measures in systemic sclerosis-associated interstitial lung disease Rheumatology (Oxford). 2023 02 06; 62(SI):SI43-SI53. . View in PubMed

Plain language summary: Clinical study of BI 1015550 as a potential treatment for idiopathic pulmonary fibrosis J Comp Eff Res. 2022 Dec 20. . View in PubMed

Thoracic Involvement in Systemic Autoimmune Rheumatic Diseases: Pathogenesis and Management Clin Rev Allergy Immunol. 2022 Dec; 63(3):472-489. . View in PubMed

Forced vital capacity trajectories in patients with idiopathic pulmonary fibrosis: a secondary analysis of a multicentre, prospective, observational cohort Lancet Digit Health. 2022 Dec; 4(12):e862-e872. . View in PubMed

Tackling the Neuropathic Cough of Idiopathic Pulmonary Fibrosis (IPF): More Needs to be Done Lung. 2022 Dec; 200(6):673-675. . View in PubMed

A review of the challenges, learnings and future directions of home handheld spirometry in interstitial lung disease Respir Res. 2022 Nov 11; 23(1):307. . View in PubMed

Diagnosis and monitoring of systemic sclerosis-associated interstitial lung disease using high-resolution computed tomography J Scleroderma Relat Disord. 2022 Oct; 7(3):168-178. . View in PubMed

Phase I studies of BI 1015550, a preferential phosphodiesterase 4B inhibitor, in healthy males and patients with idiopathic pulmonary fibrosis ERJ Open Res. 2022 Oct; 8(4). . View in PubMed

ACR Open Rheumatol. 2022 Oct; 4(10):837-844. . View in PubMed

Systemic Sclerosis Associated Interstitial Lung Disease: A Conceptual Framework for Subclinical, Clinical, and Progressive Disease Rheumatology (Oxford). 2022 Sep 29. . View in PubMed

Extent of fibrosis and lung function decline in patients with systemic sclerosis and interstitial lung disease: data from the SENSCIS trial Rheumatology (Oxford). 2022 Sep 16. . View in PubMed

Decline in forced vital capacity in subjects with systemic sclerosis-associated interstitial lung disease in the SENSCIS trial compared with healthy reference subjects Respir Res. 2022 Jul 05; 23(1):178. . View in PubMed

Cluster analysis of transcriptomic datasets to identify endotypes of idiopathic pulmonary fibrosis Thorax. 2022 May 09. . View in PubMed

PAciFy Cough-a multicentre, double-blind, placebo-controlled, crossover trial of morphine sulphate for the treatment of pulmonary Fibrosis Cough Trials. 2022 Mar 02; 23(1):184. . View in PubMed

The role of precision medicine in interstitial lung disease Eur Respir J. 2022 Feb 03. . View in PubMed

A clinical short-cut to identifying short telomeres in idiopathic pulmonary fibrosis? Respirology. 2022 11; 27(11):916-917.. View in PubMed

Genome-wide association study across five cohorts identifies five novel loci associated with idiopathic pulmonary fibrosis Thorax. 2022 08; 77(8):829-833. . View in PubMed

Meta-Analysis of Effect of Nintedanib on Reducing FVC Decline Across Interstitial Lung Diseases Adv Ther. 2022 07; 39(7):3392-3402. . View in PubMed

Lung function trajectory in progressive fibrosing interstitial lung disease Eur Respir J. 2022 06; 59(6). . View in PubMed

Short-term lung function changes predict mortality in patients with fibrotic hypersensitivity pneumonitis Respirology. 2022 03; 27(3):202-208. . View in PubMed

Pulmonary Rehabilitation in Idiopathic Pulmonary Fibrosis and COPD: A Propensity-Matched Real-World Study Chest. 2022 03; 161(3):728-737. . View in PubMed

Biomarker signatures for progressive idiopathic pulmonary fibrosis Eur Respir J. 2022 03; 59(3). . View in PubMed

Clinical Utility of Home versus Hospital Spirometry in Fibrotic Interstitial Lung Disease: Evaluation after INJUSTIS Interim Analysis Ann Am Thorac Soc. 2022 03; 19(3):506-509. . View in PubMed

Effects of nintedanib by inclusion criteria for progression of interstitial lung disease Eur Respir J. 2022 02; 59(2). . View in PubMed

Using Data on Survival with Idiopathic Pulmonary Fibrosis to Estimate Survival with Other Types of Progressive Fibrosis Interstitial Lung Disease: A Bayesian Framework Adv Ther. 2022 02; 39(2):1045-1054. . View in PubMed

Pirfenidone in Unclassifiable Interstitial Lung Disease: A Subgroup Analysis by Concomitant Mycophenolate Mofetil and/or Previous Corticosteroid Use Adv Ther. 2022 02; 39(2):1081-1095. . View in PubMed

Candidate Role for Toll-like Receptor 3 L412F Polymorphism and Infection in Acute Exacerbation of Idiopathic Pulmonary Fibrosis Am J Respir Crit Care Med. 2022 03 01; 205(5):550-562. . View in PubMed

Interstitial lung diseases Lancet. 2022 09 03; 400(10354):769-786. . View in PubMed

Phase 2B Study of Inhaled RVT-1601 for Chronic Cough in Idiopathic Pulmonary Fibrosis: A Multicenter, Randomized, Placebo-controlled Study (SCENIC Trial) Am J Respir Crit Care Med. 2022 05 01; 205(9):1084-1092. . View in PubMed

Integrating Clinical Probability into the Diagnostic Approach to Idiopathic Pulmonary Fibrosis: An International Working Group Perspective Am J Respir Crit Care Med. 2022 08 01; 206(3):247-259. . View in PubMed

CYFRA 21-1 Predicts Progression in Idiopathic Pulmonary Fibrosis: A Prospective Longitudinal Analysis of the PROFILE Cohort Am J Respir Crit Care Med. 2022 06 15; 205(12):1440-1448. . View in PubMed

Rare and Common Variants in KIF15 Contribute to Genetic Risk of Idiopathic Pulmonary Fibrosis Am J Respir Crit Care Med. 2022 07 01; 206(1):56-69. . View in PubMed

Biomarkers for Interstitial Lung Abnormalities: A Stepping-stone Toward Idiopathic Pulmonary Fibrosis Prevention? Am J Respir Crit Care Med. 2022 08 01; 206(3):244-246.. View in PubMed

Efficacy of Pirfenidone vsPlacebo in Unclassifiable Interstitial Lung Disease, by Surgical Lung Biopsy Status: Data From a post-hoc Analysis. Front Med (Lausanne). 2022; 9:897102. . View in PubMed

Trial of a Phosphodiesterase 4 Inhibitor for Idiopathic Pulmonary FibrosisReply. N Engl J Med. 2022 08 25; 387(8):762. . View in PubMed

Autoantibodies are present in the bronchoalveolar lavage but not circulation in patients with fibrotic interstitial lung disease ERJ Open Res. 2022 Jan; 8(1). . View in PubMed

Reply to Fujimoto et al: The Need for a CYFRA 21-1 Cutoff Value to Predict Clinical Progression of IPF in Clinical Practice. Am J Respir Crit Care Med. 2022 09 01; 206(5):649-650. . View in PubMed

Fatum Inexorabile: Do Monocytes Predict the Fate of Interstitial Lung Abnormalities? Am J Respir Crit Care Med. 2022 04 01; 205(7):743-744.. View in PubMed

Genome-wide Enrichment of TERT Rare Variants in Idiopathic Pulmonary Fibrosis Patients of Latino Ancestry Am J Respir Crit Care Med. 2022 10 01; 206(7):903-905. . View in PubMed

Idiopathic Pulmonary Fibrosis (an Update) and Progressive Pulmonary Fibrosis in Adults: An Official ATS/ERS/JRS/ALAT Clinical Practice Guideline Am J Respir Crit Care Med. 2022 05 01; 205(9):e18-e47. . View in PubMed

Trial of a Preferential Phosphodiesterase 4B Inhibitor for Idiopathic Pulmonary Fibrosis N Engl J Med. 2022 06 09; 386(23):2178-2187. . View in PubMed

Phase 2 trial design of BMS-986278, a lysophosphatidic acid receptor 1 (LPA1) antagonist, in patients with idiopathic pulmonary fibrosis (IPF) or progressive fibrotic interstitial lung disease (PF-ILD) BMJ Open Respir Res. 2021 Dec; 8(1). . View in PubMed

Global incidence and prevalence of idiopathic pulmonary fibrosis Respir Res. 2021 Jul 07; 22(1):197. . View in PubMed

50-gene risk profiles in peripheral blood predict COVID-19 outcomes: A retrospective, multicenter cohort study EBioMedicine. 2021 Jul; 69:103439. . View in PubMed

Worldwide experiences and opinions of healthcare providers on eHealth for patients with interstitial lung diseases in the COVID-19 era ERJ Open Res. 2021 Jul; 7(3). . View in PubMed

Respir Res. 2021 Feb 05; 22(1):38. . View in PubMed

Reply Arthritis Rheumatol. 2021 12; 73(12):2354-2355. . View in PubMed

Measurement of hypoxia in the lung in idiopathic pulmonary fibrosis: an F-MISO PET/CT study Eur Respir J. 2021 10; 58(4). . View in PubMed

Targeting Human Herpesviruses: An Effective Strategy for Treating Idiopathic Pulmonary Fibrosis? Ann Am Thorac Soc. 2021 08; 18(8):1285-1286.. View in PubMed

Circulating fibrocytes are not disease-specific prognosticators in idiopathic pulmonary fibrosis Eur Respir J. 2021 07; 58(1). . View in PubMed

Home spirometry in patients with idiopathic pulmonary fibrosis: data from the INMARK trial Eur Respir J. 2021 07; 58(1). . View in PubMed

Idiopathic pulmonary fibrosis: Disease mechanisms and drug development Pharmacol Ther. 2021 06; 222:107798. . View in PubMed

Target inhibition of galectin-3 by inhaled TD139 in patients with idiopathic pulmonary fibrosis Eur Respir J. 2021 05; 57(5). . View in PubMed

Serum markers of pulmonary epithelial damage in systemic sclerosis-associated interstitial lung disease and disease progression Respirology. 2021 05; 26(5):461-468. . View in PubMed

Effect of Nintedanib on Lung Function in Patients With Systemic Sclerosis-Associated Interstitial Lung Disease: Further Analyses of a Randomized, Double-Blind, Placebo-Controlled Trial Arthritis Rheumatol. 2021 04; 73(4):671-676. . View in PubMed

Phase 2 trial to assess lebrikizumab in patients with idiopathic pulmonary fibrosis Eur Respir J. 2021 02; 57(2). . View in PubMed

Transcriptome analysis of IPF fibroblastic foci identifies key pathways involved in fibrogenesis Thorax. 2021 01; 76(1):73-82. . View in PubMed

Efficacy and safety of nintedanib in patients with systemic sclerosis-associated interstitial lung disease treated with mycophenolate: a subgroup analysis of the SENSCIS trial Lancet Respir Med. 2021 01; 9(1):96-106. . View in PubMed

The Respiratory Microbiome in Chronic Hypersensitivity Pneumonitis Is Distinct from That of Idiopathic Pulmonary Fibrosis Am J Respir Crit Care Med. 2021 02 01; 203(3):339-347. . View in PubMed

BAL Is Safe and Well Tolerated in Individuals with Idiopathic Pulmonary Fibrosis: An Analysis of the PROFILE Study Am J Respir Crit Care Med. 2021 01 01; 203(1):136-139. . View in PubMed

Monocyte Count as a Prognostic Biomarker in Patients with Idiopathic Pulmonary Fibrosis Am J Respir Crit Care Med. 2021 07 01; 204(1):74-81. . View in PubMed

Enhanced IL-1ß Release Following NLRP3 and AIM2 Inflammasome Stimulation Is Linked to mtROS in Airway Macrophages in Pulmonary Fibrosis Front Immunol. 2021; 12:661811. . View in PubMed

Small Airways in Idiopathic Pulmonary Fibrosis: Quiet but Not Forgotten Am J Respir Crit Care Med. 2021 11 01; 204(9):1010-1011. . View in PubMed

Management of Acute Exacerbation of Idiopathic Pulmonary Fibrosis in Specialised and Non-specialised ILD Centres Around the World Front Med (Lausanne). 2021; 8:699644. . View in PubMed

DNA Methylome Alterations Are Associated with Airway Macrophage Differentiation and Phenotype during Lung Fibrosis Am J Respir Crit Care Med. 2021 10 15; 204(8):954-966. . View in PubMed

Identification of a missense variant in SPDL1 associated with idiopathic pulmonary fibrosis Commun Biol. 2021 03 23; 4(1):392. . View in PubMed

Blood Transcriptomics Predicts Progression of Pulmonary Fibrosis and Associated Natural Killer Cells Am J Respir Crit Care Med. 2021 07 15; 204(2):197-208. . View in PubMed

Muscle stimulation in advanced idiopathic pulmonary fibrosis: a randomised placebo-controlled feasibility study BMJ Open. 2021 06 02; 11(6):e048808. . View in PubMed

Proportion of Idiopathic Pulmonary Fibrosis Risk Explained by Known Common Genetic Loci in European Populations Am J Respir Crit Care Med. 2021 03 15; 203(6):775-778. . View in PubMed

Assessment of recent evidence for the management of patients with systemic sclerosis-associated interstitial lung disease: a systematic review ERJ Open Res. 2021 Jan; 7(1). . View in PubMed

Patient-centered Outcomes Research in Interstitial Lung Disease: An Official American Thoracic Society Research Statement Am J Respir Crit Care Med. 2021 07 15; 204(2):e3-e23. . View in PubMed

Itaconate controls the severity of pulmonary fibrosis Sci Immunol. 2020 Oct 23; 5(52). . View in PubMed

Author Correction: The mTORC1/4E-BP1 axis represents a critical signaling node during fibrogenesis Nat Commun. 2020 Sep 11; 11(1):4680. . View in PubMed

Shedding light on developmental drugs for idiopathic pulmonary fibrosis Expert Opin Investig Drugs. 2020 Aug; 29(8):797-808. . View in PubMed

The need for a holistic approach for SSc-ILD - achievements and ambiguity in a devastating disease Respir Res. 2020 Jul 23; 21(1):197. . View in PubMed

Chronic hypersensitivity pneumonitis; an enigmatic and frequently fatal disease Eur Respir Rev. 2020 Jun 30; 29(156). . View in PubMed

Defining genetic risk factors for scleroderma-associated interstitial lung disease : IRF5 and STAT4 gene variants are associated with scleroderma while STAT4 is protective against scleroderma-associated interstitial lung disease Clin Rheumatol. 2020 Apr; 39(4):1173-1179. . View in PubMed

A positron emission tomography imaging study to confirm target engagement in the lungs of patients with idiopathic pulmonary fibrosis following a single dose of a novel inhaled avß6 integrin inhibitor Respir Res. 2020 Mar 26; 21(1):75. . View in PubMed

Health-related quality of life and symptoms in patients with IPF treated with nintedanib: analyses of patient-reported outcomes from the INPULSIS® trials Respir Res. 2020 Jan 30; 21(1):36. . View in PubMed

Opportunities to diagnose fibrotic lung diseases in routine care: A primary care cohort study Respirology. 2020 12; 25(12):1274-1282. . View in PubMed

Safety and tolerability of nintedanib in patients with systemic sclerosis-associated interstitial lung disease: data from the SENSCIS trial Ann Rheum Dis. 2020 11; 79(11):1478-1484. . View in PubMed

Mixed Ventilatory Defects in Pulmonary Sarcoidosis: Prevalence and Clinical Features Chest. 2020 11; 158(5):2007-2014. . View in PubMed

Interaction between the promoter MUC5B polymorphism and mucin expression: is there a difference according to ILD subtype? Thorax. 2020 10; 75(10):901-903.. View in PubMed

Diagnostic and Prognostic Biomarkers for Chronic Fibrosing Interstitial Lung Diseases With a Progressive Phenotype Chest. 2020 08; 158(2):646-659. . View in PubMed

Pulmonary fibrosis secondary to COVID-19: a call to arms? Lancet Respir Med. 2020 08; 8(8):750-752.. View in PubMed

Pleuroparenchymal fibroelastosis in systemic sclerosis: prevalence and prognostic impact Eur Respir J. 2020 07; 56(1). . View in PubMed

Healthcare Resources Utilization and Costs of Patients with Non-IPF Progressive Fibrosing Interstitial Lung Disease Based on Insurance Claims in the USA Adv Ther. 2020 07; 37(7):3292-3298. . View in PubMed

Healthcare Resource Utilization Among Patients in England with Systemic Sclerosis-Associated Interstitial Lung Disease: A Retrospective Database Analysis Adv Ther. 2020 05; 37(5):2460-2476. . View in PubMed

Predictors of progression in systemic sclerosis patients with interstitial lung disease Eur Respir J. 2020 05; 55(5). . View in PubMed

Acute exacerbation of idiopathic pulmonary fibrosis: international survey and call for harmonisation Eur Respir J. 2020 04; 55(4). . View in PubMed

Clinical quantification of the integrin avß6 by [18F]FB-A20FMDV2 positron emission tomography in healthy and fibrotic human lung (PETAL Study) Eur J Nucl Med Mol Imaging. 2020 04; 47(4):967-979. . View in PubMed

Bacterial burden in the lower airways predicts disease progression in idiopathic pulmonary fibrosis and is independent of radiological disease extent Eur Respir J. 2020 04; 55(4). . View in PubMed

Physiological predictors of exertional oxygen desaturation in patients with fibrotic interstitial lung disease Eur Respir J. 2020 02; 55(2). . View in PubMed

Cost-effectiveness of ambulatory oxygen in improving quality of life in fibrotic lung disease: preliminary evidence from the AmbOx Trial Eur Respir J. 2020 02; 55(2). . View in PubMed

Pirfenidone in patients with unclassifiable progressive fibrosing interstitial lung disease: a double-blind, randomised, placebo-controlled, phase 2 trial Lancet Respir Med. 2020 02; 8(2):147-157. . View in PubMed

Genome-Wide Association Study of Susceptibility to Idiopathic Pulmonary Fibrosis Am J Respir Crit Care Med. 2020 03 01; 201(5):564-574. . View in PubMed

Treatment of Acute Exacerbation of Idiopathic Pulmonary FibrosisA Call to Arms. Am J Respir Crit Care Med. 2020 05 01; 201(9):1030-1032. . View in PubMed

Dynamics of human monocytes and airway macrophages during healthy aging and after transplant J Exp Med. 2020 03 02; 217(3). . View in PubMed

Translational pharmacology of an inhaled small molecule avß6 integrin inhibitor for idiopathic pulmonary fibrosis Nat Commun. 2020 09 16; 11(1):4659. . View in PubMed

Effect of Co-trimoxazole (Trimethoprim-Sulfamethoxazole) vs Placebo on Death, Lung Transplant, or Hospital Admission in Patients With Moderate and Severe Idiopathic Pulmonary Fibrosis: The EME-TIPAC Randomized Clinical Trial JAMA. 2020 12 08; 324(22):2282-2291. . View in PubMed

The Role of the Lung's Microbiome in the Pathogenesis and Progression of Idiopathic Pulmonary Fibrosis Int J Mol Sci. 2019 Nov 10; 20(22). . View in PubMed

Antifibrotic therapy for idiopathic pulmonary fibrosis: time to treat Respir Res. 2019 Sep 06; 20(1):205. . View in PubMed

Biomarkers of collagen synthesis predict progression in the PROFILE idiopathic pulmonary fibrosis cohort Respir Res. 2019 Jul 12; 20(1):148. . View in PubMed

Influence of Idiopathic Pulmonary Fibrosis Progression on Healthcare Resource Use Pharmacoecon Open. 2019 Mar; 3(1):81-91. . View in PubMed

Modelling Forced Vital Capacity in Idiopathic Pulmonary Fibrosis: Optimising Trial Design Adv Ther. 2019 11; 36(11):3059-3070. . View in PubMed

Current and future perspectives on management of systemic sclerosis-associated interstitial lung disease Expert Rev Clin Immunol. 2019 10; 15(10):1009-1017. . View in PubMed

Longitudinal prediction of outcome in idiopathic pulmonary fibrosis using automated CT analysis Eur Respir J. 2019 09; 54(3). . View in PubMed

King's Brief Interstitial Lung Disease questionnaire: responsiveness and minimum clinically important difference Eur Respir J. 2019 09; 54(3). . View in PubMed

Biomarkers of extracellular matrix turnover in patients with idiopathic pulmonary fibrosis given nintedanib (INMARK study): a randomised, placebo-controlled study Lancet Respir Med. 2019 09; 7(9):771-779. . View in PubMed

Potential of nintedanib in treatment of progressive fibrosing interstitial lung diseases Eur Respir J. 2019 09; 54(3). . View in PubMed

Management of Fibrosing Interstitial Lung Diseases Adv Ther. 2019 07; 36(7):1518-1531. . View in PubMed

Variable utility of mosaic attenuation to distinguish fibrotic hypersensitivity pneumonitis from idiopathic pulmonary fibrosis Eur Respir J. 2019 07; 54(1). . View in PubMed

Pirfenidone Treatment in Individuals with Idiopathic Pulmonary Fibrosis: Impact of Timing of Treatment Initiation Ann Am Thorac Soc. 2019 07; 16(7):927-930. . View in PubMed

Idiopathic Pulmonary Fibrosis: New and Emerging Treatment Options Drugs Aging. 2019 06; 36(6):485-492. . View in PubMed

Can monocytes predict prognosis of idiopathic pulmonary fibrosis? Lancet Respir Med. 2019 06; 7(6):467-469.. View in PubMed

In patients with idiopathic pulmonary fibrosis the presence of hiatus hernia is associated with disease progression and mortality Eur Respir J. 2019 05; 53(5). . View in PubMed

Patient-reported distress can aid clinical decision-making in idiopathic pulmonary fibrosis: analysis of the PROFILE cohort Eur Respir J. 2019 05; 53(5). . View in PubMed

A randomised, placebo-controlled study of omipalisib (PI3K/mTOR) in idiopathic pulmonary fibrosis Eur Respir J. 2019 03; 53(3). . View in PubMed

Regularized Latent Class Model for Joint Analysis of High-Dimensional Longitudinal Biomarkers and a Time-to-Event Outcome Biometrics. 2019 03; 75(1):69-77. . View in PubMed

Gait speed and prognosis in patients with idiopathic pulmonary fibrosis: a prospective cohort study Eur Respir J. 2019 02; 53(2). . View in PubMed

The potential impact of azithromycin in idiopathic pulmonary fibrosis Eur Respir J. 2019 02; 53(2). . View in PubMed

Proceedings of the American College of Rheumatology/Association of Physicians of Great Britain and Ireland Connective Tissue Disease-Associated Interstitial Lung Disease Summit: A Multidisciplinary Approach to Address Challenges and Opportunities Arthritis Rheumatol. 2019 02; 71(2):182-195. . View in PubMed

Predicting outcomes in rheumatoid arthritis related interstitial lung disease Eur Respir J. 2019 01; 53(1). . View in PubMed

No relevant pharmacokinetic drug-drug interaction between nintedanib and pirfenidone Eur Respir J. 2019 01; 53(1). . View in PubMed

Lung function outcomes in the INPULSIS® trials of nintedanib in idiopathic pulmonary fibrosis Respir Med. 2019 01; 146:42-48. . View in PubMed

Sarcoidosis in the UK: insights from British Thoracic Society registry data BMJ Open Respir Res. 2019; 6(1):e000357. . View in PubMed

The King's Brief Interstitial Lung Disease (KBILD) questionnaire: an updated minimal clinically important difference BMJ Open Respir Res. 2019; 6(1):e000363. . View in PubMed

The Transferrin Receptor CD71 Delineates Functionally Distinct Airway Macrophage Subsets during Idiopathic Pulmonary Fibrosis Am J Respir Crit Care Med. 2019 07 15; 200(2):209-219. . View in PubMed

The mTORC1/4E-BP1 axis represents a critical signaling node during fibrogenesis Nat Commun. 2019 01 02; 10(1):6. . View in PubMed

Diagnostic Likelihood Thresholds That Define a Working Diagnosis of Idiopathic Pulmonary Fibrosis Am J Respir Crit Care Med. 2019 11 01; 200(9):1146-1153. . View in PubMed

Computed Tomographic Biomarkers in Idiopathic Pulmonary FibrosisThe Future of Quantitative Analysis. Am J Respir Crit Care Med. 2019 01 01; 199(1):12-21. . View in PubMed

Rationale, design and objectives of two phase III, randomised, placebo-controlled studies of GLPG1690, a novel autotaxin inhibitor, in idiopathic pulmonary fibrosis (ISABELA 1 and 2) BMJ Open Respir Res. 2019; 6(1):e000422. . View in PubMed

Nintedanib for Systemic Sclerosis-Associated Interstitial Lung DiseaseReply. N Engl J Med. 2019 10 17; 381(16):1596-1597. . View in PubMed

Proceedings of the American College of Rheumatology/Association of Physicians of Great Britain and Ireland Connective Tissue Disease-Associated Interstitial Lung Disease Summit: A Multidisciplinary Approach to Address Challenges and Opportunities QJM. 2019 02 01; 112(2):81-93. . View in PubMed

Interleukin-11 is a therapeutic target in idiopathic pulmonary fibrosis Sci Transl Med. 2019 09 25; 11(511). . View in PubMed

Resequencing Study Confirms That Host Defense and Cell Senescence Gene Variants Contribute to the Risk of Idiopathic Pulmonary Fibrosis Am J Respir Crit Care Med. 2019 07 15; 200(2):199-208. . View in PubMed

Overlap of Genetic Risk between Interstitial Lung Abnormalities and Idiopathic Pulmonary Fibrosis Am J Respir Crit Care Med. 2019 12 01; 200(11):1402-1413. . View in PubMed

Nintedanib for Systemic Sclerosis-Associated Interstitial Lung Disease N Engl J Med. 2019 06 27; 380(26):2518-2528. . View in PubMed

Long-term safety of pirfenidone: results of the prospective, observational PASSPORT study ERJ Open Res. 2018 Oct; 4(4). . View in PubMed

Safety and tolerability of nintedanib for the treatment of idiopathic pulmonary fibrosis in routine UK clinical practice ERJ Open Res. 2018 Oct; 4(4). . View in PubMed

Could quality be the key in connective tissue disease-associated interstitial lung disease? Respirology. 2018 Jun 13.. View in PubMed

Improved quantitation and reproducibility in multi-PET/CT lung studies by combining CT information EJNMMI Phys. 2018 Jun 05; 5(1):14. . View in PubMed

Incidence, Prevalence, and Survival of Patients with Idiopathic Pulmonary Fibrosis in the UK Adv Ther. 2018 May; 35(5):724-736. . View in PubMed

The Efficacy and Mechanism Evaluation of Treating Idiopathic Pulmonary fibrosis with the Addition of Co-trimoxazole (EME-TIPAC): study protocol for a randomised controlled trial Trials. 2018 Feb 05; 19(1):89. . View in PubMed

Prevalence and Effects of Emphysema in Never-Smokers with Rheumatoid Arthritis Interstitial Lung Disease EBioMedicine. 2018 Feb; 28:303-310. . View in PubMed

Effect of ambulatory oxygen on quality of life for patients with fibrotic lung disease (AmbOx): a prospective, open-label, mixed-method, crossover randomised controlled trial Lancet Respir Med. 2018 10; 6(10):759-770. . View in PubMed

Gazing into the crystal ball: can treatment response be predicted in IPF? Lancet Respir Med. 2018 08; 6(8):570-572.. View in PubMed

Safety, tolerability, pharmacokinetics, and pharmacodynamics of GLPG1690, a novel autotaxin inhibitor, to treat idiopathic pulmonary fibrosis (FLORA): a phase 2a randomised placebo-controlled trial Lancet Respir Med. 2018 08; 6(8):627-635. . View in PubMed

The Burden of Illness of Idiopathic Pulmonary Fibrosis: A Comprehensive Evidence Review Pharmacoeconomics. 2018 07; 36(7):779-807. . View in PubMed

Pulmonary hypertension in interstitial lung disease: Limitations of echocardiography compared to cardiac catheterization Respirology. 2018 07; 23(7):687-694. . View in PubMed

Likelihood of pulmonary hypertension in patients with idiopathic pulmonary fibrosis and emphysema Respirology. 2018 06; 23(6):593-599. . View in PubMed

Phenotypic characteristics associated with slow gait speed in idiopathic pulmonary fibrosis Respirology. 2018 05; 23(5):498-506. . View in PubMed

Pulmonary 18F-FDG uptake helps refine current risk stratification in idiopathic pulmonary fibrosis (IPF) Eur J Nucl Med Mol Imaging. 2018 05; 45(5):806-815. . View in PubMed

Time for a change: is idiopathic pulmonary fibrosis still idiopathic and only fibrotic? Lancet Respir Med. 2018 02; 6(2):154-160.. View in PubMed

Rapidly Progressive Cystic Lung Disease Am J Respir Crit Care Med. 2018 07 15; 198(2):264. . View in PubMed

Combination Therapy and the Start of a New Epoch for Idiopathic Pulmonary Fibrosis? Am J Respir Crit Care Med. 2018 02 01; 197(3):283-284.. View in PubMed

Identifying Barriers to Idiopathic Pulmonary Fibrosis Treatment: A Survey of Patient and Physician Views Respiration. 2018; 96(6):514-524. . View in PubMed

Diverse functions of clusterin promote and protect against the development of pulmonary fibrosis Sci Rep. 2018 01 30; 8(1):1906. . View in PubMed

Predicting Outcomes in Idiopathic Pulmonary Fibrosis Using Automated Computed Tomographic Analysis Am J Respir Crit Care Med. 2018 09 15; 198(6):767-776. . View in PubMed

Pirfenidone in patients with unclassifiable progressive fibrosing interstitial lung disease: design of a double-blind, randomised, placebo-controlled phase II trial BMJ Open Respir Res. 2018; 5(1):e000289. . View in PubMed

Statin Therapy and Outcomes in Trials of Nintedanib in Idiopathic Pulmonary Fibrosis Respiration. 2018; 95(5):317-326. . View in PubMed

Metformin Does Not Affect Clinically Relevant Outcomes in Patients with Idiopathic Pulmonary Fibrosis Respiration. 2018; 96(4):314-322. . View in PubMed

The topical study of inhaled drug (salbutamol) delivery in idiopathic pulmonary fibrosis Respir Res. 2018 02 06; 19(1):25. . View in PubMed

Investigating the effects of nintedanib on biomarkers of extracellular matrix turnover in patients with IPF: design of the randomised placebo-controlled INMARK®trial BMJ Open Respir Res. 2018; 5(1):e000325. . View in PubMed

PD-1 up-regulation on CD4+ T cells promotes pulmonary fibrosis through STAT3-mediated IL-17A and TGF-ß1 production Sci Transl Med. 2018 09 26; 10(460). . View in PubMed

Pleuroparenchymal Fibroelastosis: A Review of Histopathologic Features and the Relationship Between Histologic Parameters and Survival Am J Surg Pathol. 2017 Dec; 41(12):1683-1689. . View in PubMed

Towards a global initiative for fibrosis treatment (GIFT) ERJ Open Res. 2017 Oct; 3(4). . View in PubMed

Coconut oil has less satiating properties than medium chain triglyceride oil Physiol Behav. 2017 Oct 01; 179:422-426. . View in PubMed

Unmet needs in the treatment of idiopathic pulmonary fibrosis-insights from patient chart review in five European countries BMC Pulm Med. 2017 Sep 15; 17(1):124. . View in PubMed

Validity, responsiveness and minimum clinically important difference of the incremental shuttle walk in idiopathic pulmonary fibrosis: a prospective study Thorax. 2017 Sep 07. . View in PubMed

Design of a randomised, placebo-controlled clinical trial of nintedanib in patients with systemic sclerosis-associated interstitial lung disease (SENSCIS™) Clin Exp Rheumatol. 2017 Sep-Oct; 35 Suppl 106(4):75-81. . View in PubMed

The histone deacetylase inhibitor, romidepsin, as a potential treatment for pulmonary fibrosis Oncotarget. 2017 Jul 25; 8(30):48737-48754. . View in PubMed

Nintedanib in patients with idiopathic pulmonary fibrosis and preserved lung volume Thorax. 2017 Apr; 72(4):340-346. . View in PubMed

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