Rezultati pretrage - Judith Verhoeven
- Prikaz rezultata 1 – 12 od 12
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Construction of a stereotaxic DTI atlas with full diffusion tensor information for studying white matter maturation from childhood to adolescence using tractography‐based segmentat... od Judith Verhoeven, Caroline Sage, Alexander Leemans, Wim Van Hecke, Dorothée Callaert, Ronald Peeters, Paul De Cock, Lieven Lagae, Stefan Sunaert
Izdano 2009Artigo -
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Understanding neurodevelopmental trajectories and behavioral profiles in SCN1A-related epilepsy syndromes od Amber Postma, Crista A. Minderhoud, Willem M. Otte, Floor E. Jansen, W. Boudewijn Gunning, Judith Verhoeven, Marian J. Jongmans, Janneke Zinkstok, Eva H. Brilstra
Izdano 2024Artigo -
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Altered functional connectivity of the language network in ASD: Role of classical language areas and cerebellum od 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
Izdano 2014Artigo -
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Chemotherapy‐induced structural changes in cerebral white matter and its correlation with impaired cognitive functioning in breast cancer patients od 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
Izdano 2010Artigo -
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Is There a Common Neuroanatomical Substrate of Language Deficit between Autism Spectrum Disorder and Specific Language Impairment? od 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
Izdano 2011Artigo -
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<i>SCN1A</i>-deficient excitatory neuronal networks display mutation-specific phenotypes od 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
Izdano 2023Artigo -
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Diagnostic exome sequencing in 100 consecutive patients with both epilepsy and intellectual disability od 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
Izdano 2018Artigo -
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The autism brain imaging data exchange: towards a large-scale evaluation of the intrinsic brain architecture in autism od 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
Izdano 2013Artigo -
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Defining the phenotypic spectrum of <i>SLC6A1</i> mutations od 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
Izdano 2018Artigo -
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NEXMIF encephalopathy: an X-linked disorder with male and female phenotypic patterns od 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
Izdano 2020Artigo
Alati za pretragu:
Povezani predmeti
Medicine
Neuroscience
Psychology
Audiology
Biology
Diffusion MRI
Gene
Genetics
Magnetic resonance imaging
Radiology
Autism
Autism spectrum disorder
Fractional anisotropy
Phenotype
Cognitive psychology
Developmental psychology
Epilepsy
Internal medicine
Mutation
Psychiatry
Resting state fMRI
White matter
Computer science
Dravet syndrome
Epilepsy syndromes
Functional connectivity
Functional magnetic resonance imaging
Intellectual disability
Language development
Pediatrics