检索结果 - Bertrand Chevallier

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  1. 1
    Study of phenotype evolution during childhood in Marfan syndrome to improve clinical recognition

    Study of phenotype evolution during childhood in Marfan syndrome to improve clinical recognition 由 Chantal Stheneur, Florence Tubach, Marlène Jouneaux, Carine Roy, Grégoire Benoist, Bertrand Chevallier, Cathérine Boileau, Guillaume Jondeau

    出版 2013
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  2. 2
    Safety and Reactogenicity of the 10-Valent Pneumococcal Non-typeable Haemophilus influenzae Protein D Conjugate Vaccine (PHiD-CV) When Coadministered With Routine Childhood Vaccines

    Safety and Reactogenicity of the 10-Valent Pneumococcal Non-typeable Haemophilus influenzae Protein D Conjugate Vaccine (PHiD-CV) When Coadministered With Routine Childhood Vaccine... 由 Bertrand Chevallier, Timo Vesikari, Jerzy Brzostek, Markus Knuf, Nancy Bermal, Javier Arístegui, Dorota Borys, Jan Cleerbout, Patricia Lommel, Lode Schuerman

    出版 2009
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  3. 3
    Effectiveness of Chest Physiotherapy in Infants Hospitalized with Acute Bronchiolitis: A Multicenter, Randomized, Controlled Trial

    Effectiveness of Chest Physiotherapy in Infants Hospitalized with Acute Bronchiolitis: A Multicenter, Randomized, Controlled Trial 由 Vincent Gajdos, Sandrine Katsahian, Nicole Beydon, Véronique Abadie, Loïc de Pontual, Sophie Larrar, Ralph Epaud, Bertrand Chevallier, Sylvain Bailleux, A. Mollet-Boudjemline, Jean Bouyer, Sylvie Chevret, Philippe Labrune

    出版 2010
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  4. 4
    Identification of the minimal combination of clinical features in probands for efficient mutation detection in the FBN1 gene

    Identification of the minimal combination of clinical features in probands for efficient mutation detection in the FBN1 gene 由 Chantal Stheneur, Gwenaëlle Collod‐Béroud, Laurence Faivre, Jean François Buyck, Laurent Gouya, Jean‐Marie Le Parc, Bertrand Moura, Christine Muti, Bernard Grandchamp, G. Sultan, Mireille Claustres, Philippe Aegerter, Bertrand Chevallier, Guillaume Jondeau, Cathérine Boileau

    出版 2009
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  5. 5
    Prognosis Factors in Probands With an FBN1 Mutation Diagnosed Before the Age of 1 Year

    Prognosis Factors in Probands With an FBN1 Mutation Diagnosed Before the Age of 1 Year 由 Chantal Stheneur, Laurence Faivre, Gwenaëlle Collod‐Béroud, Élodie Gautier, Christine Binquet, Claire Bonithon‐Kopp, Mireille Claustres, Anne H. Child, Eloisa Arbustini, Lesley C. Adès, Uta Francke, Karin Mayer, Mine Arslan‐Kirchner, Anne De Paepe, Bertrand Chevallier, Damien Bonnet, Guillaume Jondeau, Cathérine Boileau

    出版 2010
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  6. 6
    Identification of 23<i>TGFBR2</i>and 6<i>TGFBR1</i>gene mutations and genotype-phenotype investigations in 457 patients with Marfan syndrome type I and II, Loeys-Dietz syndrome and related disorders

    Identification of 23<i>TGFBR2</i>and 6<i>TGFBR1</i>gene mutations and genotype-phenotype investigations in 457 patients with Marfan syndrome type I and II, Loeys-Dietz syndrome and... 由 Chantal Stheneur, Gwenaëlle Collod‐Béroud, Laurence Faivre, Laurent Gouya, G. Sultan, Jean‐Marie Le Parc, Bertrand Moura, David Attias, Christine Muti, M. Sznajder, Mireille Claustres, Claudine Junien, Clarisse Baumann, Valérie Cormier‐Daire, Marlène Rio, Stanislas Lyonnet, Henri Plauchu, Didier Lacombe, Bertrand Chevallier, Guillaume Jondeau, Cathérine Boileau

    出版 2008
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  7. 7
    A big-data approach to producing descriptive anthropometric references: a feasibility and validation study of paediatric growth charts

    A big-data approach to producing descriptive anthropometric references: a feasibility and validation study of paediatric growth charts 由 Barbara Heude, Pauline Scherdel, A. Werner, Morgane Le Guern, Nathalie Gelbert, Déborah Walther, Michel Arnould, M. Bellaïche, Bertrand Chevallier, J Cheymol, Emmanuel Jobez, Sylvie Nguyen, Christine Piétrement, Rachel Reynaud, Jean‐François Salaün, Babak Khoshnood, Jennifer Zeitlin, Jean Maccario, Gérard Bréart, Jean-Christophe Thalabard, Marie‐Aline Charles, Jérémie Botton, Bruno Frandji, Martin Chalumeau

    出版 2019
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  8. 8
    Clinical and Molecular Study of 320 Children With Marfan Syndrome and Related Type I Fibrillinopathies in a Series of 1009 Probands With Pathogenic <i>FBN1</i> Mutations

    Clinical and Molecular Study of 320 Children With Marfan Syndrome and Related Type I Fibrillinopathies in a Series of 1009 Probands With Pathogenic <i>FBN1</i> Mutations 由 Laurence Faivre, Alice Masurel‐Paulet, Gwenaëlle Collod‐Béroud, Bert Callewaert, Anne H. Child, Chantal Stheneur, Christine Binquet, Élodie Gautier, Bertrand Chevallier, Frédéric Huet, Bart Loeys, Eloisa Arbustini, Karin Mayer, Mine Arslan‐Kirchner, Anatoli Kiotsekoglou, Paolo Comeglio, Maurizia Grasso, Dorothy Halliday, Christophe Béroud, Claire Bonithon‐Kopp, Mireille Claustres, Peter N. Robinson, Lesley C. Adès, Julie De Backer, Paul Coucke, Uta Francke, Anne De Paepe, Cathérine Boileau, Guillaume Jondeau

    出版 2008
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