Evaluation of a new tool for measurement of sweat chloride concentration von Hubert, D, Dusser, D.J, Bry, A, Fajac, I

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Nonclassic Cystic Fibrosis in subjects with D1152H CFTR mutation von Burgel, P.R, Fajac, I, Hubert, D, Bellis, G, Bienvenu, T, Dusser, D.J

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Telephone calls by CF nurses von Panzo, R, Agrario, L, Dupont, C, Desmazes-Dufeu, N, Kanaan, R, Burgel, P.R, Nadaud, M.J, Dusser, D.J, Hubert, D

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Pseudomonas aeruginosa induces vascular endothelial growth factor synthesis in airway epithelium in vitro and in vivo von MARTIN, C, THEVENOT, G, DANEL, S, CHAPRON, J, TAZI, A, MACEY, J, DUSSER, D. J, FAJAC, I, BURGEL, P.-R

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Undiagnosed coeliac disease in patients with emphysema: a fortuitous association? von DE MENTHON, M, DUSSER, D. J, GUILLEVIN, L, BURGEL, P. R

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Nitric oxide synthase 1 as a potential modifier gene of decline in lung function in patients with cystic fibrosis von Texereau, J, Marullo, S, Hubert, D, Coste, J, Dusser, D J, Dall’Ava-Santucci, J, Dinh-Xuan, A T

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Reduced exhaled NO is related to impaired nasal potential difference in patients with cystic fibrosis von Texereau, J., Fajac, I., Hubert, D., Coste, J., Dusser, D.J., Bienvenu, T., Dall'Ava-Santucci, J., Dinh-Xuan, A.T.

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Increased frequency of cystic fibrosis ΔF508 mutation in bronchiectasis associated with rheumatoid arthritis von Puéchal, X., Fajac, I, Bienvenu, T, Desmazes‐Dufeu, N, Hubert, D, Kaplan, J.‐C, Menkès, C.J., Dusser, D.j

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