Hasil Pencarian - Nicolas Deconinck

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  1. 1
    Cognition and communication in patients with spinal muscular atrophy: A systematic review

    Cognition and communication in patients with spinal muscular atrophy: A systematic review oleh Sanae Akodad, Delphine De Smedt, Simon Baijot, Hilde Stevens, Nicolas Deconinck

    Diterbitkan 2024-07-01
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  2. 2
    EEG Dynamics of a Go/Nogo Task in Children with ADHD

    EEG Dynamics of a Go/Nogo Task in Children with ADHD oleh Simon Baijot, Carlos Cevallos, David Zarka, Axelle Leroy, Hichem Slama, Cecile Colin, Nicolas Deconinck, Bernard Dan, Guy Cheron

    Diterbitkan 2017-12-01
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  3. 3
    Children with Autism Understand Indirect Speech Acts: Evidence from a Semi-Structured Act-Out Task.

    Children with Autism Understand Indirect Speech Acts: Evidence from a Semi-Structured Act-Out Task. oleh Mikhail Kissine, Julie Cano-Chervel, Sophie Carlier, Philippe De Brabanter, Lesley Ducenne, Marie-Charlotte Pairon, Nicolas Deconinck, Véronique Delvenne, Jacqueline Leybaert

    Diterbitkan 2015-01-01
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  4. 4
    Atypical resting-state functional brain connectivity in children with developmental coordination disorder

    Atypical resting-state functional brain connectivity in children with developmental coordination disorder oleh Dorine Van Dyck, Nicolas Deconinck, Alec Aeby, Simon Baijot, Nicolas Coquelet, Nicola Trotta, Antonin Rovai, Serge Goldman, Charline Urbain, Vincent Wens, Xavier De Tiège

    Diterbitkan 2022-01-01
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  5. 5
    Resting-state functional brain connectivity is related to subsequent procedural learning skills in school-aged children

    Resting-state functional brain connectivity is related to subsequent procedural learning skills in school-aged children oleh Dorine Van Dyck, Nicolas Deconinck, Alec Aeby, Simon Baijot, Nicolas Coquelet, Nicola Trotta, Antonin Rovai, Serge Goldman, Charline Urbain, Vincent Wens, Xavier De Tiège

    Diterbitkan 2021-10-01
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  6. 6
    Cognitive, perceptual, and motor profiles of school-aged children with developmental coordination disorder

    Cognitive, perceptual, and motor profiles of school-aged children with developmental coordination disorder oleh Dorine Van Dyck, Dorine Van Dyck, Simon Baijot, Simon Baijot, Alec Aeby, Alec Aeby, Alec Aeby, Xavier De Tiège, Xavier De Tiège, Nicolas Deconinck

    Diterbitkan 2022-08-01
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  7. 7
    Preserved coupling between the reader's voice and the listener's cortical activity in autism spectrum disorders.

    Preserved coupling between the reader's voice and the listener's cortical activity in autism spectrum disorders. oleh Catherine Clumeck, Sarah Suarez Garcia, Mathieu Bourguignon, Vincent Wens, Marc Op de Beeck, Brice Marty, Nicolas Deconinck, Marie-Vincianne Soncarrieu, Serge Goldman, Veikko Jousmäki, Patrick Van Bogaert, Xavier De Tiège

    Diterbitkan 2014-01-01
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  8. 8
    Disorder-specific brain volumetric abnormalities in Attention-Deficit/Hyperactivity Disorder relative to Autism Spectrum Disorder.

    Disorder-specific brain volumetric abnormalities in Attention-Deficit/Hyperactivity Disorder relative to Autism Spectrum Disorder. oleh Ariadna Albajara Sáenz, Peter Van Schuerbeek, Simon Baijot, Mathilde Septier, Nicolas Deconinck, Pierre Defresne, Véronique Delvenne, Gianfranco Passeri, Hubert Raeymaekers, Hichem Slama, Laurent Victoor, Eric Willaye, Philippe Peigneux, Thomas Villemonteix, Isabelle Massat

    Diterbitkan 2020-01-01
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  9. 9
    Motor Abnormalities in Attention-Deficit/Hyperactivity Disorder and Autism Spectrum Disorder Are Associated With Regional Grey Matter Volumes

    Motor Abnormalities in Attention-Deficit/Hyperactivity Disorder and Autism Spectrum Disorder Are Associated With Regional Grey Matter Volumes oleh Ariadna Albajara Sáenz, Thomas Villemonteix, Thomas Villemonteix, Peter Van Schuerbeek, Simon Baijot, Simon Baijot, Mathilde Septier, Mathilde Septier, Pierre Defresne, Véronique Delvenne, Gianfranco Passeri, Hubert Raeymaekers, Laurent Victoor, Eric Willaye, Philippe Peigneux, Nicolas Deconinck, Isabelle Massat, Isabelle Massat, Isabelle Massat, Isabelle Massat

    Diterbitkan 2021-05-01
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  10. 10
    Congenital hydrocephalus: new Mendelian mutations and evidence for oligogenic inheritance

    Congenital hydrocephalus: new Mendelian mutations and evidence for oligogenic inheritance oleh Valerie Jacquemin, Nassim Versbraegen, Sarah Duerinckx, Annick Massart, Julie Soblet, Camille Perazzolo, Nicolas Deconinck, Elise Brischoux-Boucher, Anne De Leener, Nicole Revencu, Sandra Janssens, Stèphanie Moorgat, Bettina Blaumeiser, Kristiina Avela, Renaud Touraine, Imad Abou Jaoude, Kathelijn Keymolen, Pascale Saugier-Veber, Tom Lenaerts, Marc Abramowicz, Isabelle Pirson

    Diterbitkan 2023-03-01
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  11. 11
    Upper limb evaluation and one-year follow up of non-ambulant patients with spinal muscular atrophy: an observational multicenter trial.

    Upper limb evaluation and one-year follow up of non-ambulant patients with spinal muscular atrophy: an observational multicenter trial. oleh Andreea Mihaela Seferian, Amélie Moraux, Aurélie Canal, Valérie Decostre, Oumar Diebate, Anne Gaëlle Le Moing, Teresa Gidaro, Nicolas Deconinck, Frauke Van Parys, Wendy Vereecke, Sylvia Wittevrongel, Mélanie Annoussamy, Michèle Mayer, Kim Maincent, Jean-Marie Cuisset, Vincent Tiffreau, Severine Denis, Virginie Jousten, Susana Quijano-Roy, Thomas Voit, Jean-Yves Hogrel, Laurent Servais

    Diterbitkan 2015-01-01
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  12. 12
    Three years pilot of spinal muscular atrophy newborn screening turned into official program in Southern Belgium

    Three years pilot of spinal muscular atrophy newborn screening turned into official program in Southern Belgium oleh François Boemer, Jean-Hubert Caberg, Pablo Beckers, Vinciane Dideberg, Samantha di Fiore, Vincent Bours, Sandrine Marie, Joseph Dewulf, Lionel Marcelis, Nicolas Deconinck, Aurore Daron, Laura Blasco-Perez, Eduardo Tizzano, Mickaël Hiligsmann, Jacques Lombet, Tatiana Pereira, Lucia Lopez-Granados, Sarvnaz Shalchian-Tehran, Véronique van Assche, Arabelle Willems, Sofie Huybrechts, Bénédicte Mast, Rudolf van Olden, Tamara Dangouloff, Laurent Servais

    Diterbitkan 2021-10-01
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  13. 13
    Upper limb strength and function changes during a one-year follow-up in non-ambulant patients with Duchenne Muscular Dystrophy: an observational multicenter trial.

    Upper limb strength and function changes during a one-year follow-up in non-ambulant patients with Duchenne Muscular Dystrophy: an observational multicenter trial. oleh Andreea Mihaela Seferian, Amélie Moraux, Mélanie Annoussamy, Aurélie Canal, Valérie Decostre, Oumar Diebate, Anne-Gaëlle Le Moing, Teresa Gidaro, Nicolas Deconinck, Frauke Van Parys, Wendy Vereecke, Sylvia Wittevrongel, Michèle Mayer, Kim Maincent, Isabelle Desguerre, Christine Thémar-Noël, Jean-Marie Cuisset, Vincent Tiffreau, Severine Denis, Virginie Jousten, Susana Quijano-Roy, Thomas Voit, Jean-Yves Hogrel, Laurent Servais

    Diterbitkan 2015-01-01
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  14. 14
    Novel promoters and coding first exons in DLG2 linked to developmental disorders and intellectual disability

    Novel promoters and coding first exons in DLG2 linked to developmental disorders and intellectual disability oleh Claudio Reggiani, Sandra Coppens, Tayeb Sekhara, Ivan Dimov, Bruno Pichon, Nicolas Lufin, Marie-Claude Addor, Elga Fabia Belligni, Maria Cristina Digilio, Flavio Faletra, Giovanni Battista Ferrero, Marion Gerard, Bertrand Isidor, Shelagh Joss, Florence Niel-Bütschi, Maria Dolores Perrone, Florence Petit, Alessandra Renieri, Serge Romana, Alexandra Topa, Joris Robert Vermeesch, Tom Lenaerts, Georges Casimir, Marc Abramowicz, Gianluca Bontempi, Catheline Vilain, Nicolas Deconinck, Guillaume Smits

    Diterbitkan 2017-07-01
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  15. 15
    Detection of variants in dystroglycanopathy-associated genes through the application of targeted whole-exome sequencing analysis to a large cohort of patients with unexplained limb-girdle muscle weakness

    Detection of variants in dystroglycanopathy-associated genes through the application of targeted whole-exome sequencing analysis to a large cohort of patients with unexplained limb... oleh Katherine Johnson, Marta Bertoli, Lauren Phillips, Ana Töpf, Peter Van den Bergh, John Vissing, Nanna Witting, Shahriar Nafissi, Shirin Jamal-Omidi, Anna Łusakowska, Anna Kostera-Pruszczyk, Anna Potulska-Chromik, Nicolas Deconinck, Carina Wallgren-Pettersson, Sonja Strang-Karlsson, Jaume Colomer, Kristl G. Claeys, Willem De Ridder, Jonathan Baets, Maja von der Hagen, Roberto Fernández-Torrón, Miren Zulaica Ijurco, Juan Bautista Espinal Valencia, Andreas Hahn, Hacer Durmus, Tracey Willis, Liwen Xu, Elise Valkanas, Thomas E. Mullen, Monkol Lek, Daniel G. MacArthur, Volker Straub

    Diterbitkan 2018-07-01
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  16. 16
    Phenotypes and genotypes in non‐consanguineous and consanguineous primary microcephaly: High incidence of epilepsy

    Phenotypes and genotypes in non‐consanguineous and consanguineous primary microcephaly: High incidence of epilepsy oleh Sarah Duerinckx, Julie Désir, Camille Perazzolo, Cindy Badoer, Valérie Jacquemin, Julie Soblet, Isabelle Maystadt, Yusuf Tunca, Bettina Blaumeiser, Berten Ceulemans, Winnie Courtens, François‐Guillaume Debray, Anne Destree, Koenraad Devriendt, Anna Jansen, Kathelijn Keymolen, Damien Lederer, Bart Loeys, Marije Meuwissen, Stéphanie Moortgat, Geert Mortier, Marie‐Cécile Nassogne, Tayeb Sekhara, Rudy Van Coster, Jenny Van Den Ende, Nathalie Van der Aa, Hilde Van Esch, Olivier Vanakker, Helene Verhelst, Catheline Vilain, Sarah Weckhuysen, Sandrine Passemard, Alain Verloes, Alec Aeby, Nicolas Deconinck, Patrick Van Bogaert, Isabelle Pirson, Marc Abramowicz

    Diterbitkan 2021-09-01
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