Torthaí cuardaigh - Denys Chaigne

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  1. 1
    Identification of a New Locus for Generalized Epilepsy with Febrile Seizures Plus (GEFS+) on Chromosome 2q24-q33

    Identification of a New Locus for Generalized Epilepsy with Febrile Seizures Plus (GEFS+) on Chromosome 2q24-q33 de réir Bruno Moulard, Denys Chaigne, Dominique Mouthon, Catherine Burési, Michel Guipponi, Alain Malafosse

    Foilsithe / Cruthaithe 1999
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  2. 2
    Regional cerebral glucose metabolism in epilepsies with continuous spikes and waves during sleep

    Regional cerebral glucose metabolism in epilepsies with continuous spikes and waves during sleep de réir Xavier De Tiège, Serge Goldman, Steven Laureys, Denis Verheulpen, Catherine Chiron, Catherine Wetzburger, Philippe Paquier, Denys Chaigne, Noah J. Poznanski, Isabelle Jambaqué, Édouard Hirsch, Olivier Dulac, Patrick Van Bogaert

    Foilsithe / Cruthaithe 2004
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  3. 3
    Genetic and clinical specificity of 26 symptomatic carriers for dystrophinopathies at pediatric age

    Genetic and clinical specificity of 26 symptomatic carriers for dystrophinopathies at pediatric age de réir Sandra Mercier, Annick Toutain, Aurélie Toussaint, Martine Raynaud, Claire De Barace, Pascale Marcorelles, Laurent Pasquier, Martine Blayau, Caroline Espil, P. Parent, Hubert Journel, Leïla Lazaro, Jon Andoni Urtizberea, Alexandre Moerman, Laurence Bonhomme‐Faivre, B. Eymard, Kim Maincent, Romain K. Gherardi, Denys Chaigne, Rabah Ben Yaou, France Leturcq, Jamel Chelly, Isabelle Desguerre

    Foilsithe / Cruthaithe 2013
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  4. 4
    Mutations and deletions in PCDH19 account for various familial or isolated epilepsies in females

    Mutations and deletions in PCDH19 account for various familial or isolated epilepsies in females de réir Christel Depienne, Oriane Trouillard, Delphine Bouteiller, Isabelle Gourfinkel‐An, Karine Poirier, François Rivier, Patrick Berquin, Rima Nabbout, Denys Chaigne, Dominique Steschenko, Agnès Gautier, Dorota Hoffman‐Zacharska, Annie Lannuzel, Marilyn Lackmy-Port-Lis, Hélène Maurey, A. Dusser, Marie Bru, Brigitte Gilbert‐Dussardier, Agathe Roubertie, Anna Kaminśka, Sandra Whalen, Cyril Mignot, Stéphanie Baulac, Gaëtan Lesca, Alexis Arzimanoglou, Eric Leguern

    Foilsithe / Cruthaithe 2010
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  5. 5
    Early onset collagen VI myopathies: Genetic and clinical correlations

    Early onset collagen VI myopathies: Genetic and clinical correlations de réir Laura Briñas, Pascale Richard, Susana Quijano‐Roy, Corine Gartioux, C. Ledeuil, Emmanuelle Lacène, S. Makri, Ana Ferreiro, Svetlana Maugenre, Haluk Topaloğlu, Göknur Haliloğlu, I. Pénisson-Besnier, Pierre‐Yves Jeannet, Luciano Merlini, Carmen Navarro, Annick Toutain, Denys Chaigne, Isabelle Desguerre, Christine de Die‐Smulders, Murielle Dunand, Bernard Échenne, B. Eymard, Thierry Küntzer, Kim Maincent, M. Mayer, Ghislaine Plessis, François Rivier, Filip Roelens, Tanya Stojkovic, Ana Lía Taratuto, Fabiana Lubieniecki, Soledad Monges, Christine Tranchant, Louis Viollet, Norma B. Romero, B. Estournet, Pascale Guicheney, Valérie Allamand

    Foilsithe / Cruthaithe 2010
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  6. 6
    The clinical, histologic, and genotypic spectrum of <i>SEPN1</i> -related myopathy

    The clinical, histologic, and genotypic spectrum of <i>SEPN1</i> -related myopathy de réir Rocío N. Villar‐Quiles, Maja von der Hagen, Corinne Métay, Victoria González, Sandra Donkervoort, Enrico Bertini, Claudia Castiglioni, Denys Chaigne, Jaume Colomer, María L. Cuadrado, Marianne de Visser, Isabelle Desguerre, B. Eymard, Nathalie Goemans, Angela M. Kaindl, Emmanuelle Lagrue, Jürg Lütschg, Edoardo Malfatti, M. Mayer, Luciano Merlini, David Orlikowski, Ulrike Reuner, Mustafa A. Salih, Beate Schlotter‐Weigel, Mechthild Stoetter, Volker Straub, Haluk Topaloğlu, J. Andoni Urtizberea, Anneke J. van der Kooi, Ekkehard Wilichowski, Norma B. Romero, Michel Fardeau, Carsten G. Bönnemann, B. Estournet, Pascale Richard, Susana Quijano‐Roy, Ulrike Schara, Ana Ferreiro

    Foilsithe / Cruthaithe 2020
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