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Pirfenidone for idiopathic pulmonary fibrosis: analysis of pooled data from three multinational phase 3 trials

The European respiratory journal, 2016-01, Vol.47 (1), p.243-253

2016

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Predictors of mortality in rheumatoid arthritis-associated interstitial lung disease

The European respiratory journal, 2016-02, Vol.47 (2), p.588-596

2016

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Identifying Barriers to Idiopathic Pulmonary Fibrosis Treatment: A Survey of Patient and Physician Views

Respiration, 2018-11, Vol.96 (6), p.514-524

2018

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Mycophenolate mofetil improves lung function in connective tissue disease-associated interstitial lung disease

Journal of rheumatology, 2013-05, Vol.40 (5), p.640-646

2013

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Sarcoidosis-related Mortality in the United States from 1988 to 2007

American journal of respiratory and critical care medicine, 2011-06, Vol.183 (11), p.1524-1530

2011

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Rheumatoid Arthritis―Interstitial Lung Disease―associated Mortality

American journal of respiratory and critical care medicine, 2011-02, Vol.183 (3), p.372-378

2011

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The Clinical Course of Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia

Chest, 2015-02, Vol.147 (2), p.415-422

2015

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Identifying an Inciting Antigen Is Associated With Improved Survival in Patients With Chronic Hypersensitivity Pneumonitis

Chest, 2013-11, Vol.144 (5), p.1644-1651

2013

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The 6 minute walk in idiopathic pulmonary fibrosis: longitudinal changes and minimum important difference

Thorax, 2010-02, Vol.65 (2), p.173-177

2010

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High resolution computed tomography pattern of usual interstitial pneumonia in rheumatoid arthritis-associated interstitial lung disease: Relationship to survival

Respiratory medicine, 2017-05, Vol.126, p.100-104

2017

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Health-related quality of life in patients with idiopathic pulmonary fibrosis: a systematic review

Thorax, 2005-07, Vol.60 (7), p.588-594

2005

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Development and validity testing of an IPF-specific version of the St George's Respiratory Questionnaire

Thorax, 2010-10, Vol.65 (10), p.921-926

2010

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Pulmonary Function and Survival in Idiopathic vs Secondary Usual Interstitial Pneumonia

Chest, 2014-09, Vol.146 (3), p.775-785

2014

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A Multidisciplinary Evaluation Helps Identify the Antisynthetase Syndrome in Patients Presenting as Idiopathic Interstitial Pneumonia

Journal of rheumatology, 2016-05, Vol.43 (5), p.887-892

2016

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Effect of pirfenidone on mortality: pooled analyses and meta-analyses of clinical trials in idiopathic pulmonary fibrosis

The lancet respiratory medicine, 2017-01, Vol.5 (1), p.33-41

2017

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Pulmonary fibrosis is associated with an elevated risk of thromboembolic disease

The European respiratory journal, 2012-01, Vol.39 (1), p.125-132

2012

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Mortality from Pulmonary Fibrosis Increased in the United States from 1992 to 2003

American journal of respiratory and critical care medicine, 2007-08, Vol.176 (3), p.277-284

2007

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Patient-Reported Outcomes in Idiopathic Pulmonary Fibrosis Research

Chest, 2012-08, Vol.142 (2), p.291-297

2012

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Understanding the determinants of health-related quality of life in rheumatoid arthritis-associated interstitial lung disease

Respiratory medicine, 2017-06, Vol.127, p.1-6

2017

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The SF-36 and SGRQ: Validity and first look at minimum important differences in IPF

Respiratory medicine, 2010-02, Vol.104 (2), p.296-304

2010

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A first look at the reliability, validity and responsiveness of L-PF-35 dyspnea domain scores in fibrotic hypersensitivity pneumonitis

BMC pulmonary medicine, 2024-04, Vol.24 (1), p.188-8, Article 188

2024

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Patients' perceptions and patient-reported outcomes in progressive-fibrosing interstitial lung diseases

European respiratory review, 2018-12, Vol.27 (150), p.180075

2018

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Increasing Hypersensitivity Pneumonitis-related Mortality in the United States from 1988 to 2016

American journal of respiratory and critical care medicine, 2019-05, Vol.199 (10), p.1284-1287

2019

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Managing Cough in Idiopathic Pulmonary Fibrosis

Chest, 2021-11, Vol.160 (5), p.1774-1782

2021

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The UCSD shortness of breath questionnaire has longitudinal construct validity in idiopathic pulmonary fibrosis

Respiratory medicine, 2012-10, Vol.106 (10), p.1447-1455

2012

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Pirfenidone for idiopathic pulmonary fibrosis: analysis of pooled data from three multinational phase 3 trials

Predictors of mortality in rheumatoid arthritis-associated interstitial lung disease

Identifying Barriers to Idiopathic Pulmonary Fibrosis Treatment: A Survey of Patient and Physician Views

Mycophenolate mofetil improves lung function in connective tissue disease-associated interstitial lung disease

Sarcoidosis-related Mortality in the United States from 1988 to 2007

Rheumatoid Arthritis―Interstitial Lung Disease―associated Mortality

The Clinical Course of Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia

Identifying an Inciting Antigen Is Associated With Improved Survival in Patients With Chronic Hypersensitivity Pneumonitis

The 6 minute walk in idiopathic pulmonary fibrosis: longitudinal changes and minimum important difference

High resolution computed tomography pattern of usual interstitial pneumonia in rheumatoid arthritis-associated interstitial lung disease: Relationship to survival

Health-related quality of life in patients with idiopathic pulmonary fibrosis: a systematic review

Development and validity testing of an IPF-specific version of the St George's Respiratory Questionnaire

Pulmonary Function and Survival in Idiopathic vs Secondary Usual Interstitial Pneumonia

A Multidisciplinary Evaluation Helps Identify the Antisynthetase Syndrome in Patients Presenting as Idiopathic Interstitial Pneumonia

Effect of pirfenidone on mortality: pooled analyses and meta-analyses of clinical trials in idiopathic pulmonary fibrosis

Pulmonary fibrosis is associated with an elevated risk of thromboembolic disease

Mortality from Pulmonary Fibrosis Increased in the United States from 1992 to 2003

Patient-Reported Outcomes in Idiopathic Pulmonary Fibrosis Research

Understanding the determinants of health-related quality of life in rheumatoid arthritis-associated interstitial lung disease

The SF-36 and SGRQ: Validity and first look at minimum important differences in IPF

A first look at the reliability, validity and responsiveness of L-PF-35 dyspnea domain scores in fibrotic hypersensitivity pneumonitis

Patients' perceptions and patient-reported outcomes in progressive-fibrosing interstitial lung diseases

Increasing Hypersensitivity Pneumonitis-related Mortality in the United States from 1988 to 2016

Managing Cough in Idiopathic Pulmonary Fibrosis

The UCSD shortness of breath questionnaire has longitudinal construct validity in idiopathic pulmonary fibrosis

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