Search Results - "du Bois, R.M"

BAL findings in idiopathic nonspecific interstitial pneumonia and usual interstitial pneumonia by Veeraraghavan, S, Latsi, P.I, Wells, A.U, Pantelidis, P, Nicholson, A.G, Colby, T.V, Haslam, P.L, Renzoni, E.A, du Bois, R.M

“…Idiopathic pulmonary fibrosis (IPF), which has the histological pattern of usual interstitial pneumonia (UIP), is a progressive interstitial lung disease with…”
Get full text

CC and C chemokine expression in pulmonary sarcoidosis by Petrek, M, Kolek, V, Szotkowska, J, du Bois, R.M

“…The chemokines RANTES (regulated on activation, T-cell expressed and secreted; CC chemokine ligand (CCL)-5) and monocyte inflammatory protein (MIP)-1alpha…”
Get full text

Idiopathic pulmonary fibrosis: present understanding and future options by du Bois, R M

Get full text

Idiopathic pulmonary fibrosis: Now less idiopathic? by du Bois, R.M

“…Idiopathic pulmonary fibrosis (IPF) is a progressive diffuse fibrosing lung disease that kills increasing numbers of individuals each year with levels of…”
Get full text

CC chemokine receptor 5 gene polymorphisms in beryllium disease by SATO, H, SILVEIRA, L, SPAGNOLO, P, GILLESPIE, M, GOTTSCHATT, E. B, WELSH, K. I, DU BOIS, R. M, NEWMAN, L. S, MAIER, L. A

“…CC chemokine receptor 5 (CCR5) is expressed on type-1 T-helper cells, which are involved in the pathogenesis of the granulomatous lung disease chronic…”
Get full text

Autocrine Overexpression of CTGF Maintains Fibrosis: RDA Analysis of Fibrosis Genes in Systemic Sclerosis by Shi-wen, X., Pennington, D., Holmes, A., Leask, A., Bradham, D., Beauchamp, J.R., Fonseca, C., du Bois, R.M., Martin, G.R., Black, C.M., Abraham, D.J.

“…We have used representational difference analysis (RDA) to identify up-regulated genes in skin fibroblasts from fibrotic lesions obtained from patients with…”
Get full text

Cryptogenic fibrosing alveolitis/idiopathic pulmonary fibrosis by du Bois, R.M, Wells, A.U

“…Cryptogenic fibrosing alveolitis (CFA), synonymous with idiopathic pulmonary fibrosis (IPF), remains a life-threatening disease: 50% of patients die within 5…”
Get full text

Interferon Gamma-1b for the Treatment of Idiopathic Pulmonary Fibrosis by Bois, R.M. du

“…Idiopathic pulmonary fibrosis is a chronic condition of the lung parenchyma involving progressive injury, inflammation, and fibrosis. Data collected from…”
Get full text

Strategies for treating idiopathic pulmonary fibrosis by du Bois, R. M

“…Key Points Idiopathic pulmonary fibrosis (IPF) is the most common form of idiopathic interstitial pneumonia (IIP), a group of diseases of unknown cause that…”
Get full text

Genetic predisposition and pathogenetic mechanisms of interstitial lung diseases of unknown origin by Verleden, G.M, du Bois, R.M, Bouros, D, Drent, M, Millar, A, Muller-Quernheim, J, Semenzato, G, Johnson, S, Sourvinos, G, Olivieri, D, Pietinalho, A, Xaubet, A

“…Understanding of the cellular and cytokine interactions associated with inflammation and fibrosis in interstitial lung diseases (ILDs) has increased…”
Get full text

An earlier and more confident diagnosis of idiopathic pulmonary fibrosis by du Bois, Roland M

“…A diagnosis of idiopathic pulmonary fibrosis (IPF) has serious implications for the affected individuals, who have a 50% likelihood of dying within 2-3 yrs, an…”
Get full text

Increased vitronectin and endothelin-1 in the breath condensate of patients with fibrosing lung disease by Carpagnano, G E, Kharitonov, S A, Wells, A U, Pantelidis, P, Du Bois, R M, Barnes, P J

“…Non-specific interstitial pneumonia (NSIP) and fibrosing alveolitis associated with systemic sclerosis (FASSc) are diseases of unknown aetiology that are…”
Get more information

Primary epithelioid angiosarcoma of the lung presenting as pulmonary hemorrhage by Sheppard, M.N, Hansell, D.M, Du Bois, R.M, Nicholson, A.G

“…Pulmonary angiosarcomas are usually secondary tumors, and only a few primary cases have been described. We report a unique case of epithelioid angiosarcoma…”
Get full text

Observer variation in pattern type and extent of disease in fibrosing alveolitis on thin section computed tomography and chest radiography by Collins, C D, Wells, A U, Hansell, D M, Morgan, R A, MacSweeney, J E, du Bois, R M, Rubens, M B

“…In fibrosing alveolitis the pattern type on thin section computed tomography (CT) predicts histological appearances at open lung biopsy and the likelihood of…”
Get more information

Genetic commonality between inflammatory bowel disease and sarcoidosis: the beginning of the end or the end of the beginning?: Figure 1 by Cerri, S., du Bois, R.M., Spagnolo, P.

Get full text

Idiopathic pulmonary fibrosis trials: recommendations for the jury by Nathan, S D, du Bois, R M

Get full text

T-helper cell type-1 transcription factor T-bet is upregulated in pulmonary sarcoidosis by KRIEGOVA, E, FILLEROVA, R, TOMANKOVA, T, HUTYROVA, B, MRAZEK, F, TICHY, T, KOLEK, V, DU BOIS, R. M, PETREK, M

“…Upregulation of genes for interferon (IFN)-γ and CXC chemokine receptor (CXCR)3 expression, two crucial molecules in sarcoid inflammation and granuloma…”
Get full text

Increased epithelial permeability in pulmonary fibrosis in relation to disease progression by GOH, N. S. L, DESAI, S. R, ANAGNOSTOPOULOS, C, HANSELL, D. M, HOYLES, R. K, SATO, H, DENTON, C. P, BLACK, C. M, DU BOIS, R. M, WELLS, A. U

“…Epithelial injury contributes to pathogenesis in idiopathic pulmonary fibrosis (IPF) but its role in the interstitial lung disease (ILD) of systemic sclerosis…”
Get full text

Acute interstitial pneumonia by Bouros, D, Nicholson, AC, Polychronopoulos, V, du Bois, RM

“…The term “acute interstitial pneumonia” (AIP) describes an idiopathic clinicopathological condition, characterized clinically by an interstitial lung disease…”
Get full text

Protein levels of CC chemokine ligand (CCL)15, CCL16 and macrophage stimulating protein in patients with sarcoidosis by Arakelyan, A, Kriegova, E, Kubištova, Z, Mrazek, F, Kverka, M, du Bois, R.M, Kolek, V, Petrek, M

“…The objective of this study was to assess protein levels for candidate cytokines, chemokines, growth factors, matrix metalloproteinases and their inhibitors in…”
Get full text