Search Results - M.‐P. Audrézet

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  1. 1
    A Conservative Assessment of the Major Genetic Causes of Idiopathic Chronic Pancreatitis: Data from a Comprehensive Analysis of PRSS1, SPINK1, CTRC and CFTR Genes in 253 Young French Patients

    A Conservative Assessment of the Major Genetic Causes of Idiopathic Chronic Pancreatitis: Data from a Comprehensive Analysis of PRSS1, SPINK1, CTRC and CFTR Genes in 253 Young Fren... by Emmanuelle Masson, Jian‐Min Chen, M.‐P. Audrézet, D.N. Cooper, Claude Férec

    Published 2013
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  2. 2
    Mutations in GANAB , Encoding the Glucosidase IIα Subunit, Cause Autosomal-Dominant Polycystic Kidney and Liver Disease

    Mutations in GANAB , Encoding the Glucosidase IIα Subunit, Cause Autosomal-Dominant Polycystic Kidney and Liver Disease by Binu Porath, Vladimir G. Gainullin, Émilie Cornec-Le Gall, Elizabeth K. Dillinger, Christina M. Heyer, Katharina Hopp, Marie E. Edwards, Charles D. Madsen, Sarah R. Mauritz, Carly J. Banks, Saurabh Baheti, Bharathi Reddy, J.I. Herrero, Jesús M. Bañales, Marie C. Hogan, Velibor Tasić, Terry Watnick, Arlene B. Chapman, Cécile Vigneau, Frédéric Lavainne, M.‐P. Audrézet, Claude Férec, Yannick Le Meur, Vicente E. Torres, Peter C. Harris

    Published 2016
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  3. 3
    PKD2 -Related Autosomal Dominant Polycystic Kidney Disease: Prevalence, Clinical Presentation, Mutation Spectrum, and Prognosis

    PKD2 -Related Autosomal Dominant Polycystic Kidney Disease: Prevalence, Clinical Presentation, Mutation Spectrum, and Prognosis by Émilie Cornec-Le Gall, M.‐P. Audrézet, E. Renaudineau, Maryvonne Hourmant, Christophe Charasse, E. Michez, T. Frouget, Cécile Vigneau, Jacques Dantal, P. Siohan, Hélène Longuet, Philippe Gatault, Laure Écotière, Frank Bridoux, Lise Mandart, Catherine Hanrotel‐Saliou, C. Stanescu, Pascale Depraêtre, Sophie Gié, M Massad, Aude Kersalé, Guillaume Séret, Jean‐François Augusto, Philippe Saliou, Sandrine Maestri, Jian‐Min Chen, Peter C. Harris, Claude Férec, Yannick Le Meur

    Published 2017
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  4. 4
    The very low penetrance of cystic fibrosis for the R117H mutation: a reappraisal for genetic counselling and newborn screening

    The very low penetrance of cystic fibrosis for the R117H mutation: a reappraisal for genetic counselling and newborn screening by Christel Thauvin‐Robinet, À. Munck, Frédéric Huet, Emmanuelle Génin, Gil Bellis, Élodie Gautier, M-P Audrezet, Claude Férec, G. Lalau, M. des Georges, M. Claustres, Thierry Bienvenu, Bénédicte Gérard, Pierre Boisseau, Faïza Cabet-Bey, D Feldmann, Christine Clavel, Éric Bieth, A. Iron, Brigitte Simon‐Bouy, C Costa, R.A. Medina López, Julie Leclerc, D. Hubert, R. Nové-Josserand, Isabelle Sermet‐Gaudelus, G. Rault, J Flori, Sabine Léroy, Nathalie Wizla, G. Bellon, A. Haloun, S. Bui, G. Dacremont, Harriet Corvol, Albrecht M. Clement, Elise Houssin, Christine Binquet, Claire Bonithon‐Kopp, C. Alberti-Boulmé, Michael A. Morris, Laurence Faivre, M. Goossens, M. Roussey

    Published 2009
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