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

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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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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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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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Genetics of fibrosing lung diseases von Grutters, J. C, du 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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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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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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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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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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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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Exhaled Nitric Oxide Is Increased in Active Fibrosing Alveolitis von Paredi, Paolo, Kharitonov, S.A., Loukides, S., Pantelidis, P., Bois, R. M. du, Barnes, Peter J.

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

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