CFTR‐France, a national relational patient database for sharing genetic and phenotypic data associated with rare CFTR variants von Claustres, Mireille, Thèze, Corinne, des Georges, Marie, Baux, David, Girodon, Emmanuelle, Bienvenu, Thierry, Audrezet, Marie‐Pierre, Dugueperoux, Ingrid, Férec, Claude, Lalau, Guy, Pagin, Adrien, Kitzis, Alain, Thoreau, Vincent, Gaston, Véronique, Bieth, Eric, Malinge, Marie‐Claire, Reboul, Marie‐Pierre, Fergelot, Patricia, Lemonnier, Lydie, Mekki, Chadia, Fanen, Pascale, Bergougnoux, Anne, Sasorith, Souphatta, Raynal, Caroline, Bareil, Corinne

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Clinical Changes of Patients with Cystic Fibrosis during Transition from Pediatric to Adult Care von Duguépéroux, Ingrid, Ph.D, Tamalet, Aline, M.D, Sermet-Gaudelus, Isabelle, M.D., Ph.D, Le Bourgeois, Muriel, M.D, Gérardin, Michèle, M.D, Desmazes-Dufeu, Nadine, M.D, Hubert, Dominique, M.D

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Evidence for decline in the incidence of cystic fibrosis: a 35-year observational study in Brittany, France von Scotet, Virginie, Duguépéroux, Ingrid, Saliou, Philippe, Rault, Gilles, Roussey, Michel, Audrézet, Marie-Pierre, Férec, Claude

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Focus on cystic fibrosis and other disorders evidenced in fetuses with sonographic finding of echogenic bowel: 16-year report from Brittany, France von Scotet, Virginie, PhD, Duguépéroux, Ingrid, PhD, Audrézet, Marie-Pierre, PhD, Audebert-Bellanger, Séverine, MD, Muller, Matthieu, MD, Blayau, Martine, MD, Férec, Claude, MD, PhD

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Misprocessing of the CFTR protein leads to mild cystic fibrosis phenotype von Clain, Jérôme, Lehmann-Che, Jacqueline, Duguépéroux, Ingrid, Arous, Nicole, Girodon, Emmanuelle, Legendre, Marie, Goossens, Michel, Edelman, Aleksander, de Braekeleer, Marc, Teulon, Jacques, Fanen, Pascale

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Highlighting the impact of cascade carrier testing in cystic fibrosis families von Duguépéroux, Ingrid, L'Hostis, Carine, Audrézet, Marie-Pierre, Rault, Gilles, Frachon, Irène, Bernard, Rémy, Parent, Philippe, Blayau, Martine, Schmitt, Sébastien, Génin, Emmanuelle, Férec, Claude, Scotet, Virginie

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Spatial and temporal distribution of cystic fibrosis and of its mutations in Brittany, France: a retrospective study from 1960 von SCOTET, Virginie, GILLET, Dominique, FEREC, Claude, DUGUEPEROUX, Ingrid, AUDREZET, Marie-Pierre, BELLIS, Gil, GARNIER, Bénédicte, ROUSSEY, Michel, RAULT, Gilles, PARENT, Philippe, DE BRAEKELEER, Marc

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CFTR -France, a national relational patient database for sharing genetic and phenotypic data associated with rare CFTR variants von Claustres, Mireille, Thèze, Corinne, Des Georges, Marie, Baux, David, Girodon, Emmanuelle, Bienvenu, Thierry, Audrezet, Marie-Pierre, Dugueperoux, Ingrid, Férec, Claude, Lalau, Guy, Pagin, Adrien, Kitzis, Alain, Thoreau, Vincent, Gaston, Véronique, Bieth, Eric, Malinge, Marie-Claire, Reboul, Marie-Pierre, Fergelot, Patricia, Lemonnier, Lydie, Mekki, Chadia, Fanen, Pascale, Bergougnoux, Anne, Sasorith, Souphatta, Raynal, Caroline, Bareil, Corinne

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CFTR -France, a national relational patient database for sharing genetic and phenotypic data associated with rare CFTR variants von Claustres, Mireille, Thèze, Corinne, Des Georges, Marie, Baux, David, Girodon, Emmanuelle, Bienvenu, Thierry, Audrezet, Marie-Pierre, Dugueperoux, Ingrid, Férec, Claude, Lalau, Guy, Pagin, Adrien, Kitzis, Alain, Thoreau, Vincent, Gaston, Véronique, Bieth, Eric, Malinge, Marie-Claire, Reboul, Marie-Pierre, Fergelot, Patricia, Lemonnier, Lydie, Mekki, Chadia, Fanen, Pascale, Bergougnoux, Anne, Sasorith, Souphatta, Raynal, Caroline, Bareil, Corinne

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Nonvisualization of fetal gallbladder increases the risk of cystic fibrosis von Duguépéroux, Ingrid, Scotet, Virginie, Audrézet, Marie-Pierre, Saliou, Anne-Hélène, Collet, Michel, Blayau, Martine, Schmitt, Sébastien, Kitzis, Alain, Fresquet, Fleur, Müller, Françoise, Férec, Claude

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Time Trends in Birth Incidence of Cystic Fibrosis in Two European Areas: Data from Newborn Screening Programs von Scotet, Virginie, PhD, Assael, Baroukh M., MD, Duguépéroux, Ingrid, PhD, Tamanini, Anna, PhD, Audrézet, Marie-Pierre, PhD, Férec, Claude, MD, PhD, Castellani, Carlo, MD

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Relationship of non-visualization of the fetal gallbladder and amniotic fluid digestive enzymes analysis to outcome von Dreux, Sophie, Boughanim, Mathias, Lepinard, Catherine, Guichet, Agnès, Rival, Jean-Marie, de Becdelievre, Alix, Dugueperoux, Ingrid, Muller, Françoise

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Cascade testing in families of carriers identified through newborn screening in Western Brittany (France) von Duguépéroux, Ingrid, Audrézet, Marie-Pierre, Parent, Philippe, Audebert-Bellanger, Séverine, Roussey, Michel, Férec, Claude, Scotet, Virginie

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Prenatal diagnosis of cystic fibrosis: the 18-year experience of Brittany (western France) von Scotet, Virginie, Duguépéroux, Ingrid, Audrézet, Marie-Pierre, Blayau, Martine, Boisseau, Pierre, Journel, Hubert, Parent, Philippe, Férec, Claude

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Paternity in men with cystic fibrosis: a retrospective survey in France von Duguépéroux, Ingrid, Hubert, Dominique, Dominique, Stéphane, Bellis, Gil, De Braekeleer, Marc, Durieu, Isabelle

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Pulmonary outcome differences in U.S. and French cystic fibrosis cohorts diagnosed through newborn screening von Walsh, Aimee C, Rault, Gilles, Li, Zhanhai, Scotet, Virginie, Duguépéroux, Ingrid, Férec, Claude, Roussey, Michel, Laxova, Anita, Farrell, Philip M

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Original article: Clinical Changes of Patients with Cystic Fibrosis during Transition from Pediatric to Adult Care von Dugueperoux, Ingrid, Tamalet, Aline, Sermet-Gaudelus, Isabelle, Le Bourgeois, Muriel, Gerardin, Michele, Desmazes-Dufeu, Nadine, Hubert, Dominique

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Neonatal screening for cystic fibrosis in Brittany, France: assessment of 10 years' experience and impact on prenatal diagnosis von Scotet, Virginie, de Braekeleer, Marc, Roussey, Michel, Rault, Gilles, Parent, Philippe, Dagorne, Michel, Journel, Hubert, Lemoigne, Auguste, Codet, Jean-Pierre, Catheline, Michel, David, Véronique, Chaventré, André, Duguépéroux, Ingrid, Verlingue, Claudine, Quéré, Isabelle, Mercier, Bernard, Audrézet, Marie-Pierre, Férec, Claude

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Genotype–phenotype relationship for five CFTR mutations frequently identified in western France von Duguépéroux, Ingrid, De Braekeleer, Marc

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Misprocessing of the CFTR protein leads to mild cystic fibrosis phenotype: MISPROCESSING OF CFTR AND MILD PHENOTYPE von Clain, Jérôme, Lehmann-Che, Jacqueline, Duguépéroux, Ingrid, Arous, Nicole, Girodon, Emmanuelle, Legendre, Marie, Goossens, Michel, Edelman, Aleksander, de Braekeleer, Marc, Teulon, Jacques, Fanen, Pascale

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