Search Results - Yves Chaix

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  1. 1
    What Do We Really Know About Motor Learning in Children with Developmental Coordination Disorder?

    What Do We Really Know About Motor Learning in Children with Developmental Coordination Disorder? by Maëlle Biotteau, Yves Chaix, Jean‐Michel Albaret

    Published 2016
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  2. 2
    Can the Cognitive Phenotype in Neurofibromatosis Type 1 (NF1) Be Explained by Neuroimaging? A Review

    Can the Cognitive Phenotype in Neurofibromatosis Type 1 (NF1) Be Explained by Neuroimaging? A Review by Éloïse Baudou, Federico Nemmi, Maëlle Biotteau, Stéphanie Maziero, Patrice Péran, Yves Chaix

    Published 2020
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  3. 3
    Neural Signature of DCD: A Critical Review of MRI Neuroimaging Studies

    Neural Signature of DCD: A Critical Review of MRI Neuroimaging Studies by Maëlle Biotteau, Yves Chaix, Mélody Blais, Jessica Tallet, Patrice Péran, Jean‐Michel Albaret

    Published 2016
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  4. 4
    <p>Developmental coordination disorder and dysgraphia: signs and symptoms, diagnosis, and rehabilitation</p>

    <p>Developmental coordination disorder and dysgraphia: signs and symptoms, diagnosis, and rehabilitation</p> by Maëlle Biotteau, Jérémy Danna, Éloïse Baudou, Frédéric Puyjarinet, Jean‐Luc Velay, Jean‐Michel Albaret, Yves Chaix

    Published 2019
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  5. 5
    Systematic MRI in NF1 children under six years of age for the diagnosis of optic pathway gliomas. Study and outcome of a French cohort

    Systematic MRI in NF1 children under six years of age for the diagnosis of optic pathway gliomas. Study and outcome of a French cohort by Gaëlle Blanchard, Marie-Pierre Lafforgue, Laurence Lion‐François, Isabelle Kemlin, Diana Rodriguez, Pierre Castelnau, Maryline Carneiro, Pierre Meyer, François Rivier, S. Barbarot, Yves Chaix

    Published 2015
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  6. 6
    Human TRAF3 Adaptor Molecule Deficiency Leads to Impaired Toll-like Receptor 3 Response and Susceptibility to Herpes Simplex Encephalitis

    Human TRAF3 Adaptor Molecule Deficiency Leads to Impaired Toll-like Receptor 3 Response and Susceptibility to Herpes Simplex Encephalitis by Rebeca Pérez de Diego, Vanessa Sancho‐Shimizu, Lazaro Lorenzo, Anne Puel, Sabine Plancoulaine, Capucine Pïcard, Melina Herman, Annabelle Cardon, Anne Durandy, Jacinta Bustamante, Sivakumar Vallabhapurapu, Jerónimo Bravo, Klaus Warnatz, Yves Chaix, Françoise Cascarrigny, Pierre Lebon, Flore Rozenberg, Michael Karin, Marc Tardieu, Saleh Al‐Muhsen, Emmanuelle Jouanguy, Shen‐Ying Zhang, Laurent Abel, Jean‐Laurent Casanova

    Published 2010
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  7. 7
    Phenotypic variability in ARCA2 and identification of a core ataxic phenotype with slow progression

    Phenotypic variability in ARCA2 and identification of a core ataxic phenotype with slow progression by Cyril Mignot, Emmanuelle Apartis, Alexandra Dürr, Charles Marques Lourenço, Perrine Charles, David Devos, Caroline Moreau, Pascale de Lonlay, Nathalie Drouot, Lydie Bürglen, Nadine Kempf, Elsa Nourisson, Sandra Chantot‐Bastaraud, Anne-Sophie Lèbre, Marlène Rio, Yves Chaix, Éric Bieth, Emmanuel Roze, I Bonnet, Sandrine Canaple, Coralie Rastel, Alexis Brice, Agnès Rötig, Isabelle Desguerre, Christine Tranchant, Michel Kœnig, Mathieu Anheim

    Published 2013
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  8. 8
    Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort

    Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort by Jessica Becker, Darina Czamara, Tom S. Scerri, Franck Ramus, Valéria Csépe, Joel B. Talcott, John Stein, Andrew P. Morris, Kerstin U. Ludwig, Per Hoffmann, Ferenc Honbolygó, Dénes Tóth, Fabien Fauchereau, Caroline Bogliotti, Stéphanie Iannuzzi, Yves Chaix, Sylviane Valdois, C. Billard, Florence George, Isabelle Soares‐Boucaud, Christophe‐Loïc Gérard, Sanne van der Mark, Enrico Schulz, Anniek Vaessen, Urs Maurer, Kaisa Lohvansuu, Heikki Lyytinen, Marco Zucchelli, Daniel Brandeis, Leo Blomert, Paavo H. T. Leppänen, Jennifer Bruder, Anthony P. Monaco, Bertram Müller‐Myhsok, Juha Kere, Karin Landerl, Markus M. Nöthen, Gerd Schulte‐Körne, Silvia Paracchini, Myriam Peyrard‐Janvid, Johannes Schumacher

    Published 2013
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  9. 9
    Predictors of developmental dyslexia in European orthographies with varying complexity

    Predictors of developmental dyslexia in European orthographies with varying complexity by Karin Landerl, Franck Ramus, Kristina Moll, Heikki Lyytinen, Paavo H. T. Leppänen, Kaisa Lohvansuu, Michael O’Donovan, Julie Williams, Jürgen Bartling, Jennifer Bruder, Sarah Kunze, Nina Neuhoff, Dénes Tóth, Ferenc Honbolygó, Valéria Csépe, Caroline Bogliotti, Stéphanie Iannuzzi, Yves Chaix, Jean‐François Démonet, Emilie Longeras, Sylviane Valdois, Camille Chabernaud, F. Delteil-Pinton, C. Billard, Florence George, Johannes C. Ziegler, Isabelle Comte-Gervais, Isabelle Soares‐Boucaud, Christophe‐Loïc Gérard, Leo Blomert, Anniek Vaessen, Patty Gerretsen, Michel Ekkebus, Daniel Brandeis, Urs Maurer, Enrico Schulz, Sanne van der Mark, Bertram Müller‐Myhsok, Gerd Schulte‐Körne

    Published 2012
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  10. 10
    Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia

    Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia by Alessandro Gialluisi, Till F. M. Andlauer, Nazanin Mirza‐Schreiber, Kristina Moll, Jessica Becker, Per Hoffmann, Kerstin U. Ludwig, Darina Czamara, Beaté St Pourcain, Ferenc Honbolygó, Dénes Tóth, Valéria Csépe, Guillaume Huguet, Yves Chaix, Stéphanie Iannuzzi, Jean‐François Démonet, Andrew P. Morris, Jacqueline Hulslander, Erik G. Willcutt, John C. DeFries, Richard K. Olson, Shelley D. Smith, Bruce F. Pennington, Anniek Vaessen, Urs Maurer, Heikki Lyytinen, Myriam Peyrard‐Janvid, Paavo H. T. Leppänen, Daniel Brandeis, Milene Bonte, John Stein, Joel B. Talcott, Fabien Fauchereau, Arndt Wilcke, Holger Kirsten, Bent Müller, Clyde Francks, Thomas Bourgeron, Anthony P. Monaco, Franck Ramus, Karin Landerl, Juha Kere, Thomas Scerri, Silvia Paracchini, Simon E. Fisher, Johannes Schumacher, Markus M. Nöthen, Bertram Müller‐Myhsok, Gerd Schulte‐Körne

    Published 2020
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