Clinical significance of Scedosporium apiospermum in patients with cystic fibrosis von CIMON, B, CARRERE, J, VINATIER, J. F, CHAZALETTE, J. P, CHABASSE, D, BOUCHARA, J. P

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Production of elastase, exotoxin A, and alkaline protease in sputa during pulmonary exacerbation of cystic fibrosis in patients chronically infected by Pseudomonas aeruginosa von JAFFAR-BANDJEE, M. C, LAZDUNSKI, A, BALLY, M, CARRERE, J, CHAZALETTE, J. P, GALABERT, C

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Complex allele [-102T>A+S549R(T>G)] is associated with milder forms of cystic fibrosis than allele S549R(T>G) alone von ROMEY, M.-C, GUITTARD, C, BOZON, D, SEGURET, F, DEMAILLE, J, CLAUSTRES, M, CHAZALETTE, J.-P, FROSSARD, P, DAWSON, K. P, PATTON, M. A, CASALS, T, BAZARBACHI, T, GIRODON, E, RAULT, G

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Chronic airway colonization by Penicillium emersonii in a patient with cystic fibrosis von CIMON, B, CARRERE, J, CHAZALETTE, J. P, VINATIER, J. F, CHABASSE, D, BOUCHARA, J. P

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Effects of ursodeoxycholic acid on liver function in patients with cystic fibrosis and chronic cholestasis von Galabert, C., Montet, J.C., Lengrand, D., Lecuire, A., Sotta, C., Figarella, C., Chazalette, J.P.

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Improvement of cystic fibrosis airway mucus transportability by recombinant human DNase is related to changes in phospholipid profile von ZAHM, J.-M, GALABERT, C, CHAFFIN, A, CHAZALETTE, J.-P, GROSSKOPF, C, PUCHELLE, E

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Multicenter Study of Prevalence of Nontuberculous Mycobacteria in Patients with Cystic Fibrosis in France von Roux, Anne-Laure, Catherinot, Emilie, Ripoll, Fabienne, Soismier, Nathalie, Macheras, Edouard, Ravilly, Sophie, Bellis, Gil, Vibet, Marie-Anne, Le Roux, Evelyne, Lemonnier, Lydie, Gutierrez, Cristina, Vincent, Véronique, Fauroux, Brigitte, Rottman, Martin, Guillemot, Didier, Gaillard, Jean-Louis

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Mutation analysis in 600 French cystic fibrosis patients von Chevalier-Porst, F, Bonardot, A M, Gilly, R, Chazalette, J P, Mathieu, M, Bozon, D

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Cystic Fibrosis and Portal Hypertension Interest of Partial Splenectomy von Louis, D., Chazalette, J. -P.

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Partial splenectomy—worth the risk von Chazalette, J P, Feigelson, J, Louis, D

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Mycobacterium avium and Mycobacterium abscessus complex target distinct cystic fibrosis patient subpopulations von Catherinot, Emilie, Roux, Anne-Laure, Vibet, Marie-Anne, Bellis, Gil, Ravilly, Sophie, Lemonnier, Lydie, Le Roux, Evelyne, Bernède-Bauduin, Claire, Le Bourgeois, Muriel, Herrmann, Jean-Louis, Guillemot, Didier, Gaillard, Jean-Louis

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Inhaled therapies, azithromycin and Mycobacterium abscessus in cystic fibrosis patients von CATHERINOT, Emilie, ROUX, Anne-Laure, GAILLARD, Jean-Louis, VIBET, Marie-Anne, BELLIS, Gil, LEMONNIER, Lydie, LE ROUX, Evelyne, BERNEDE-BAUDUIN, Claire, LE BOURGEOIS, Muriel, HERRMANN, Jean-Louis, GUILLEMOT, Didier

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Lysinuric protein intolerance. Urinary amino acid excretion at 2 and 9 days of age von Candito, M., Vianey‐Saban, C., Ferraci, J. P., Bébin, B., Chazalette, J. P., Sebag, F., Mathieu, M., Chambon, P.

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Imaging Changes in the Pancreas in Cystic Fibrosis: A Retrospective Evaluation of 55 Cases Seen Over a Period of 9 Years von Feigelson, Jean, Pécau, Yvette, Poquet, Myriam, Terdjman, Patricia, Carrère, Jacqueline, Chazalette, Jean‐Pierre, Ferec, Claude

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Efficacy of Pancrease: Crossover Comparative Study versus Eurobiol in Cystic Fibrosis von Chazalette, J-P, Dain, M P, Castaigne, J-P

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40 kilobase deletion (CF 40 kb del 4-10) removes exons 4 to 10 of the cystic fibrosis transmembrane conductance regulator gene von Chevalier-Porst, Françoise, Bonardot, Anne-Marie, Chazalette, Jean-Pierre, Mathieu, Monique, Bozon, Dominique

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Prise en charge des manifestations otorhinolaryngologiques von Coste, A., Triglia, J.M., Nicollas, R., Chazalette, J.P., Ravilly, S.

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Agénésie déférentielle bilatérale et hernie inguinale chez un enfant. Une présentation précoce rare de la mucoviscidose von Merrot, T, Delarue, A, Chaumoitre, K, Panuel, M, Sigaudy, S, Chazalette, J.P, Alessandrini, P

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Management of otorhinolaryngeal manifestations von Coste, A, Triglia, J M, Nicollas, R, Chazalette, J P, Ravilly, S

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Prise en charge des manifestations otorhinolaryngologiques: Recommandations pour la prise en charge de la mucoviscidose von COSTE, A, TRIGLIA, J. M, NICOLLAS, R, CHAZALETTE, J. P, RAVILLY, S

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