Výsledky vyhledávání - Judith Verhoeven

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  1. 1
    Integrity of the inferior longitudinal fasciculus and impaired object recognition in children: a diffusion tensor imaging study

    Integrity of the inferior longitudinal fasciculus and impaired object recognition in children: a diffusion tensor imaging study Autor Els Ortibus, Judith Verhoeven, Stefan Sunaert, Ingele Casteels, Paul De Cock, Lieven Lagae

    Vydáno 2011
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  2. 2
    Structural and functional underconnectivity as a negative predictor for language in autism

    Structural and functional underconnectivity as a negative predictor for language in autism Autor Marjolein Verly, Judith Verhoeven, Inge Zink, Dante Mantini, Lukas Van Oudenhove, Lieven Lagae, Stefan Sunaert, Nathalie Rommel

    Vydáno 2013
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  3. 3
    Construction of a stereotaxic DTI atlas with full diffusion tensor information for studying white matter maturation from childhood to adolescence using tractography‐based segmentations

    Construction of a stereotaxic DTI atlas with full diffusion tensor information for studying white matter maturation from childhood to adolescence using tractography‐based segmentat... Autor Judith Verhoeven, Caroline Sage, Alexander Leemans, Wim Van Hecke, Dorothée Callaert, Ronald Peeters, Paul De Cock, Lieven Lagae, Stefan Sunaert

    Vydáno 2009
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  4. 4
    Understanding neurodevelopmental trajectories and behavioral profiles in SCN1A-related epilepsy syndromes

    Understanding neurodevelopmental trajectories and behavioral profiles in SCN1A-related epilepsy syndromes Autor Amber Postma, Crista A. Minderhoud, Willem M. Otte, Floor E. Jansen, W. Boudewijn Gunning, Judith Verhoeven, Marian J. Jongmans, Janneke Zinkstok, Eva H. Brilstra

    Vydáno 2024
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  5. 5
    Altered functional connectivity of the language network in ASD: Role of classical language areas and cerebellum

    Altered functional connectivity of the language network in ASD: Role of classical language areas and cerebellum Autor Marjolein Verly, Judith Verhoeven, Inge Zink, Dante Mantini, Ronald Peeters, Sabine Deprez, Louise Emsell, Bart Boets, Ilse Noens, Jean Steyaert, Lieven Lagae, Paul De Cock, Nathalie Rommel, Stefan Sunaert

    Vydáno 2014
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  6. 6
    Chemotherapy‐induced structural changes in cerebral white matter and its correlation with impaired cognitive functioning in breast cancer patients

    Chemotherapy‐induced structural changes in cerebral white matter and its correlation with impaired cognitive functioning in breast cancer patients Autor Sabine Deprez, Frédéric Amant, Refika Yigit, Kathleen Porke, Judith Verhoeven, Jan Van den Stock, Ann Smeets, Marie‐Rose Christiaens, Alexander Leemans, Wim Van Hecke, Joris Vandenberghe, Mathieu Vandenbulcke, Stefan Sunaert

    Vydáno 2010
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  7. 7
    Is There a Common Neuroanatomical Substrate of Language Deficit between Autism Spectrum Disorder and Specific Language Impairment?

    Is There a Common Neuroanatomical Substrate of Language Deficit between Autism Spectrum Disorder and Specific Language Impairment? Autor Judith Verhoeven, Nathalie Rommel, Elena Prodi, Alexander Leemans, Inge Zink, Evelien Vandewalle, Ilse Noens, Johan Wagemans, Jean Steyaert, Bart Boets, Ann Van de Winckel, Paul De Cock, Lieven Lagae, Stefan Sunaert

    Vydáno 2011
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  8. 8
    <i>SCN1A</i>-deficient excitatory neuronal networks display mutation-specific phenotypes

    <i>SCN1A</i>-deficient excitatory neuronal networks display mutation-specific phenotypes Autor Eline van Hugte, Elly Lewerissa, Ka Man Wu, Nicky Scheefhals, Giulia Parodi, Torben W. van Voorst, Sophie Puvogel, Naoki Kogo, Jason M. Keller, Monica Frega, Dirk Schubert, Helenius J. Schelhaas, Judith Verhoeven, Marian Majoie, Hans van Bokhoven, Nael Nadif Kasri

    Vydáno 2023
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  9. 9
    Diagnostic exome sequencing in 100 consecutive patients with both epilepsy and intellectual disability

    Diagnostic exome sequencing in 100 consecutive patients with both epilepsy and intellectual disability Autor Francesca M. Snoeijen‐Schouwenaars, Jans S. van Ool, Judith Verhoeven, Petra van Mierlo, Hilde M. H. Braakman, Eric Smeets, Joost Nicolai, Jeroen Schoots, Mariël W.A. Teunissen, Rob P.W. Rouhl, Francis Tan, Helger G. Yntema, Han G. Brunner, Rolph Pfundt, Alexander P.A. Stegmann, Erik‐Jan Kamsteeg, Helenius J. Schelhaas, Marjolein H. Willemsen

    Vydáno 2018
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  10. 10
    The autism brain imaging data exchange: towards a large-scale evaluation of the intrinsic brain architecture in autism

    The autism brain imaging data exchange: towards a large-scale evaluation of the intrinsic brain architecture in autism Autor Adriana Di Martino, Chao‐Gan Yan, Q Li, E Denio, F. Xavier Castellanos, Kaat Alaerts, Jeffrey S. Anderson, Michal Assaf, Susan Y. Bookheimer, Mirella Dapretto, Ben Deen, Sonja Delmonte, Ilan Dinstein, Birgit Ertl‐Wagner, Damien A. Fair, Louise Gallagher, Daniel P. Kennedy, Christopher L. Keown, Christian Keysers, Janet E. Lainhart, Catherine Lord, Beatríz Luna, Vinod Menon, Nancy J. Minshew, Christopher S. Monk, Sophia Mueller, R. Müller, Mary Beth Nebel, Joel T. Nigg, Kirsten O’Hearn, Kevin A. Pelphrey, Scott Peltier, Jeffrey D. Rudie, Stefan Sunaert, Marc Thioux, J. Michael Tyszka, Lucina Q. Uddin, Judith Verhoeven, Nicole Wenderoth, Jillian Lee Wiggins, Stewart H. Mostofsky, Michael P. Milham

    Vydáno 2013
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  11. 11
    Defining the phenotypic spectrum of <i>SLC6A1</i> mutations

    Defining the phenotypic spectrum of <i>SLC6A1</i> mutations Autor Katrine M. Johannesen, Elena Gardella, Tarja Linnankivi, Carolina Courage, Anne de Saint Martin, Anna‐Elina Lehesjoki, Cyril Mignot, Alexandra Afenjar, Gaëtan Lesca, Marie‐Thérèse Abi‐Warde, Jamel Chelly, Amélie Piton, J. Lawrence Merritt, Lance H. Rodan, Wen‐Hann Tan, Lynne M. Bird, Mark Nespeca, Joseph G. Gleeson, Yongjin Yoo, Murim Choi, Jong‐Hee Chae, Desiree Czapansky-Beilman, Sara Reichert, Manuela Pendziwiat, Judith Verhoeven, Helenius J. Schelhaas, Orrin Devinsky, Jakob Christensen, Nicola Specchio, Marina Trivisano, Yvonne G. Weber, Caroline Nava, Boris Keren, Diane Doummar, Élise Schaefer, Sarah Hopkins, Holly Dubbs, Jessica Shaw, Laura Rosa Pisani, Candace T. Myers, Sha Tang, Shan Tang, Deb K. Pal, J Gordon Millichap, Gemma L. Carvill, Kathrine L. Helbig, Oriano Mecarelli, Pasquale Striano, Ingo Helbig, Guido Rubboli, Heather C. Mefford, Rikke S. Møller

    Vydáno 2018
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  12. 12
    NEXMIF encephalopathy: an X-linked disorder with male and female phenotypic patterns

    NEXMIF encephalopathy: an X-linked disorder with male and female phenotypic patterns Autor Hannah Stamberger, Trine Bjørg Hammer, Elena Gardella, Danique R.M. Vlaskamp, Birgitte Bertelsen, Simone Mandelstam, Iris Lange, Jing Zhang, Candace T. Myers, Christina Fenger, Zaid Afawi, Edith P. Almanza Fuerte, Danielle M. Andrade, Yunus Balcik, Bruria Ben Zeev, Mark F. Bennett, Samuel F. Berkovic, Bertrand Isidor, Arjan Bouman, Eva H. Brilstra, Øyvind L. Busk, Anita Cairns, Roseline Caumes, Nicolas Chatron, Russell C. Dale, Christa de Geus, Patrick Edery, Deepak Gill, Jacob Bie Granild-Jensen, Lauren Gunderson, Boudewijn Gunning, Gali Heimer, Johan Robert Helle, Michael S. Hildebrand, Georgie Hollingsworth, Volodymyr Kharytonov, Eric W. Klee, Bobby P.C. Koeleman, David A. Koolen, Christian Korff, Sébastien Küry, Gaëtan Lesca, Dorit Lev, Richard J. Leventer, Mark T. Mackay, Erica L. Macke, Meriel McEntagart, Shekeeb S. Mohammad, Pauline Monin, Martino Montomoli, Éva Morava, Sébastien Moutton, Alison M. Muir, Elena Parrini, Peter Procopis, Emmanuelle Ranza, Laura Reed, Philipp S. Reif, Felix Rosenow, Massimiliano Rossi, Lynette G. Sadleir, Tara Sadoway, Helenius J. Schelhaas, Amy L. Schneider, Krati Shah, Ruth S. Shalev, Sanjay M. Sisodiya, Thomas Smol, Connie T. R. M. Stumpel, Kyra E. Stuurman, Joseph D. Symonds, Frédéric Tran Mau‐Them, Nienke E. Verbeek, Judith Verhoeven, Geoff Wallace, Keren Yosovich, Yuri A. Zárate, Ayelet Zerem, Sameer M. Zuberi, Renzo Guerrini, Heather C. Mefford, Chirag Patel, Yue-Hua Zhang, Rikke S. Møller, Ingrid E. Scheffer

    Vydáno 2020
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