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Strategies for treating idiopathic pulmonary fibrosis

Nature reviews. Drug discovery, 2010-02, Vol.9 (2), p.129-140

du Bois, R. M

2010

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Approaches to the treatment of some of the troublesome manifestations of sarcoidosis

Journal of internal medicine, 2014-04, Vol.275 (4), p.335-349

2014

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Increased epithelial permeability in pulmonary fibrosis in relation to disease progression

The European respiratory journal, 2011-07, Vol.38 (1), p.184-190

2011

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Echocardiography and pulmonary function as screening tests for pulmonary arterial hypertension in systemic sclerosis

British journal of rheumatology, 2004-04, Vol.43 (4), p.461-466

2004

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Variations in histological patterns of interstitial pneumonia between connective tissue disorders and their relationship to prognosis

Histopathology, 2004-06, Vol.44 (6), p.585-596

2004

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Genetics of fibrosing lung diseases

The European respiratory journal, 2005-05, Vol.25 (5), p.915-927

2005

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Genetic mutations in surfactant protein C are a rare cause of sporadic cases of IPF

Thorax, 2004-11, Vol.59 (11), p.977-980

2004

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T-helper cell type-1 transcription factor T-bet is upregulated in pulmonary sarcoidosis

The European respiratory journal, 2011-11, Vol.38 (5), p.1136-1144

2011

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BAL findings in idiopathic nonspecific interstitial pneumonia and usual interstitial pneumonia

The European respiratory journal, 2003-08, Vol.22 (2), p.239-244

2003

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Desquamative interstitial pneumonia, respiratory bronchiolitis and their relationship to smoking

Histopathology, 2004-09, Vol.45 (3), p.275-282

2004

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Pulmonary involvement by Niemann-Pick disease. A report of six cases

Histopathology, 2006-04, Vol.48 (5), p.596-603

2006

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Clinical significance of respiratory bronchiolitis on open lung biopsy and its relationship to smoking related interstitial lung disease

Thorax, 1999-11, Vol.54 (11), p.1009-1014

1999

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Protein levels of CC chemokine ligand (CCL)15, CCL16 and macrophage stimulating protein in patients with sarcoidosis

Clinical and experimental immunology, 2009-03, Vol.155 (3), p.457-465

2009

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A common haplotype of the C‐C chemokine receptor 2 gene and HLA‐DRB10301 are independent genetic risk factors for Löfgren’s syndrome

Journal of internal medicine, 2008-11, Vol.264 (5), p.433-441

2008

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Is there a role for microorganisms in the pathogenesis of sarcoidosis?

Journal of internal medicine, 2003-01, Vol.253 (1), p.4-17

2003

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CARD15/NOD2 polymorphisms are associated with severe pulmonary sarcoidosis

The European respiratory journal, 2010-02, Vol.35 (2), p.324-330

2010

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Multiplex immune serum biomarker profiling in sarcoidosis and systemic sclerosis

The European respiratory journal, 2009-12, Vol.34 (6), p.1376-1382

2009

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Acute interstitial pneumonia

The European respiratory journal, 2000-02, Vol.15 (2), p.412-418

2000

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An earlier and more confident diagnosis of idiopathic pulmonary fibrosis

European respiratory review, 2012-06, Vol.21 (124), p.141-146

du Bois, Roland M

2012

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Quality of life and dyspnoea in patients treated with bosentan for idiopathic pulmonary fibrosis (BUILD-1)

The European respiratory journal, 2010-01, Vol.35 (1), p.118-123

2010

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Nonspecific interstitial pneumonia and usual interstitial pneumonia: comparative appearances at and diagnostic accuracy of thin-section CT

Radiology, 2001-12, Vol.221 (3), p.600-605

2001

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Increased levels of endothelin-1 and differential endothelin type A and B receptor expression in scleroderma-associated fibrotic lung disease

The American journal of pathology, 1997-09, Vol.151 (3), p.831-841

1997

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CC and C chemokine expression in pulmonary sarcoidosis

The European respiratory journal, 2002-11, Vol.20 (5), p.1206-1212

2002

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Serial CT in fibrosing alveolitis: prognostic significance of the initial pattern

American journal of roentgenology (1976), 1993-12, Vol.161 (6), p.1159-1165

1993

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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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Strategies for treating idiopathic pulmonary fibrosis

Approaches to the treatment of some of the troublesome manifestations of sarcoidosis

Increased epithelial permeability in pulmonary fibrosis in relation to disease progression

Echocardiography and pulmonary function as screening tests for pulmonary arterial hypertension in systemic sclerosis

Variations in histological patterns of interstitial pneumonia between connective tissue disorders and their relationship to prognosis

Genetics of fibrosing lung diseases

Genetic mutations in surfactant protein C are a rare cause of sporadic cases of IPF

T-helper cell type-1 transcription factor T-bet is upregulated in pulmonary sarcoidosis

BAL findings in idiopathic nonspecific interstitial pneumonia and usual interstitial pneumonia

Desquamative interstitial pneumonia, respiratory bronchiolitis and their relationship to smoking

Pulmonary involvement by Niemann-Pick disease. A report of six cases

Clinical significance of respiratory bronchiolitis on open lung biopsy and its relationship to smoking related interstitial lung disease

Protein levels of CC chemokine ligand (CCL)15, CCL16 and macrophage stimulating protein in patients with sarcoidosis

A common haplotype of the C‐C chemokine receptor 2 gene and HLA‐DRB10301 are independent genetic risk factors for Löfgren’s syndrome

Is there a role for microorganisms in the pathogenesis of sarcoidosis?

CARD15/NOD2 polymorphisms are associated with severe pulmonary sarcoidosis

Multiplex immune serum biomarker profiling in sarcoidosis and systemic sclerosis

Acute interstitial pneumonia

An earlier and more confident diagnosis of idiopathic pulmonary fibrosis

Quality of life and dyspnoea in patients treated with bosentan for idiopathic pulmonary fibrosis (BUILD-1)

Nonspecific interstitial pneumonia and usual interstitial pneumonia: comparative appearances at and diagnostic accuracy of thin-section CT

Increased levels of endothelin-1 and differential endothelin type A and B receptor expression in scleroderma-associated fibrotic lung disease

CC and C chemokine expression in pulmonary sarcoidosis

Serial CT in fibrosing alveolitis: prognostic significance of the initial pattern

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

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