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

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Marginal decline in forced vital capacity is associated with a poor outcome in idiopathic pulmonary fibrosis von Zappala, C. J, Latsi, P. I, Nicholson, A. G, Colby, T. V, Cramer, D, Renzoni, E. A, Hansell, D. M, du Bois, R. M, Wells, A. U

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Approaches to the treatment of some of the troublesome manifestations of sarcoidosis von Eklund, A., Bois, R. M.

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Echocardiography and pulmonary function as screening tests for pulmonary arterial hypertension in systemic sclerosis von Mukerjee, D., St. George, D., Knight, C., Davar, J., Wells, A. U., Du Bois, R. M., Black, C. M., Coghlan, J. G.

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Variations in histological patterns of interstitial pneumonia between connective tissue disorders and their relationship to prognosis von Tansey, D, Wells, A U, Colby, T V, Ip, S, Nikolakoupolou, A, Du Bois, R M, Hansell, D M, Nicholson, A G

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Increased epithelial permeability in pulmonary fibrosis in relation to disease progression von 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

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

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Genetic mutations in surfactant protein C are a rare cause of sporadic cases of IPF von Lawson, W E, Grant, S W, Ambrosini, V, Womble, K E, Dawson, E P, Lane, K B, Markin, C, Renzoni, E, Lympany, P, Thomas, A Q, Roldan, J, Scott, T A, Blackwell, T S, Phillips, J A, Loyd, J E, du Bois, R M

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Genetics of fibrosing lung diseases von Grutters, J. C, du Bois, R. M

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Pulmonary involvement by Niemann-Pick disease. A report of six cases von Nicholson, A G, Florio, R, Hansell, D M, du Bois, R M, Wells, A U, Hughes, P, Ramadan, H K, Mackinlay, C I, Brambilla, E, Ferretti, G R, Erichsen, A, Malone, M, Lantuejoul, S

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CARD15/NOD2 polymorphisms are associated with severe pulmonary sarcoidosis von Sato, H, Williams, H. R. T, Spagnolo, P, Abdallah, A, Ahmad, T, Orchard, T. R, Copley, S. J, Desai, S. R, Wells, A. U, du Bois, R. M, Welsh, K. I

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BAL findings in idiopathic nonspecific interstitial pneumonia and usual interstitial pneumonia von 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

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Multiplex immune serum biomarker profiling in sarcoidosis and systemic sclerosis von Beirne, P, Pantelidis, P, Charles, P, Wells, A. U, Abraham, D. J, Denton, C. P, Welsh, K. I, Shah, P. L, du Bois, R. M, Kelleher, P

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Desquamative interstitial pneumonia, respiratory bronchiolitis and their relationship to smoking von Craig, P J, Wells, A U, Doffman, S, Rassl, D, Colby, T V, Hansell, D M, Du Bois, R M, Nicholson, A G

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Quality of life and dyspnoea in patients treated with bosentan for idiopathic pulmonary fibrosis (BUILD-1) von Raghu, G, King, T. E., Jr, Behr, J, Brown, K. K, du Bois, R. M, Leconte, I, Roux, S, Swigris, J

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Clinical significance of respiratory bronchiolitis on open lung biopsy and its relationship to smoking related interstitial lung disease von Moon, James, du Bois, Ronald M, Colby, Thomas V, Hansell, David M, Nicholson, Andrew G

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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 von Spagnolo, P., Sato, H., Grunewald, J., Brynedal, B., Hillert, J., Mañá, J., Wells, A. U., Eklund, A., Welsh, K. I., Du Bois, R. M.

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Is there a role for microorganisms in the pathogenesis of sarcoidosis? von Du Bois, R. M., Goh, N., McGrath, D., Cullinan, P.

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

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

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