Longitudinal Assessment of Chemotherapy-Induced Structural Changes in Cerebral White Matter and Its Correlation With Impaired Cognitive Functioning
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Published in Journal of clinical oncology (20.01.2012)
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Cardiac arrhythmias in Dravet syndrome: an observational multicenter study
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Diagnostic exome sequencing in 100 consecutive patients with both epilepsy and intellectual disability
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Verhoeven, Judith S., De Cock, Paul, Lagae, Lieven, Sunaert, Stefan
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Postma, Amber, Minderhoud, Crista A., Otte, Wim M., Jansen, Floor E., Gunning, W.B., Verhoeven, Judith S., Jongmans, Marian J., Zinkstok, Janneke R., Brilstra, Eva H.
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Failure of ketogenic diet therapy in GLUT1 deficiency syndrome
Bekker, Yvonne A.C., Lambrechts, Danielle A., Verhoeven, Judith S., van Boxtel, Jessy, Troost, Caroline, Kamsteeg, Erik-Jan, Willemsen, Michèl A., Braakman, Hilde M.H.
Published in European journal of paediatric neurology (01.05.2019)
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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 segmentations
Verhoeven, Judith S., Sage, Caroline A., Leemans, Alexander, Van Hecke, Wim, Callaert, Dorothée, Peeters, Ronald, De Cock, Paul, Lagae, Lieven, Sunaert, Stefan
Published in Human brain mapping (01.03.2010)
Published in Human brain mapping (01.03.2010)
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Is there a common neuroanatomical substrate of language deficit between autism spectrum disorder and specific language impairment?
Verhoeven, Judith S, Rommel, Nathalie, Prodi, Elena, Leemans, Alexander, Zink, Inge, Vandewalle, Ellen, Noens, Ilse, Wagemans, Johan, Steyaert, Jean, Boets, Bart, Van de Winckel, Ann, De Cock, Paul, Lagae, Lieven, Sunaert, Stefan
Published in Cerebral cortex (New York, N.Y. 1991) (01.10.2012)
Published in Cerebral cortex (New York, N.Y. 1991) (01.10.2012)
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Quality of life in SCN1A-related seizure disorders across the lifespan
Minderhoud, Crista A, Postma, Amber, Jansen, Floor E, Zinkstok, Janneke R, Verhoeven, Judith S, Berghuis, Bianca, Otte, Wim M, Jongmans, Marian J, Braun, Kees P J, Brilstra, Eva H
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Phenytoin as a last-resort treatment in SCN8A encephalopathy
Braakman, Hilde M, Verhoeven, Judith S, Erasmus, Corrie E, Haaxma, Charlotte A, Willemsen, Marjolein H, Schelhaas, H Jurgen
Published in Epilepsia open (01.09.2017)
Published in Epilepsia open (01.09.2017)
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Phenytoin as a last‐resort treatment in SCN 8A encephalopathy
Braakman, Hilde M., Verhoeven, Judith S., Erasmus, Corrie E., Haaxma, Charlotte A., Willemsen, Marjolein H., Schelhaas, H. Jurgen
Published in Epilepsia open (01.09.2017)
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The autism brain imaging data exchange: towards a large-scale evaluation of the intrinsic brain architecture in autism
Di Martino, A, Yan, C-G, Li, Q, Denio, E, Castellanos, F X, Alaerts, K, Anderson, J S, Assaf, M, Bookheimer, S Y, Dapretto, M, Deen, B, Delmonte, S, Dinstein, I, Ertl-Wagner, B, Fair, D A, Gallagher, L, Kennedy, D P, Keown, C L, Keysers, C, Lainhart, J E, Lord, C, Luna, B, Menon, V, Minshew, N J, Monk, C S, Mueller, S, Müller, R-A, Nebel, M B, Nigg, J T, O'Hearn, K, Pelphrey, K A, Peltier, S J, Rudie, J D, Sunaert, S, Thioux, M, Tyszka, J M, Uddin, L Q, Verhoeven, J S, Wenderoth, N, Wiggins, J L, Mostofsky, S H, Milham, M P
Published in Molecular psychiatry (01.06.2014)
Published in Molecular psychiatry (01.06.2014)
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Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implications
Johannesen, Katrine M, Liu, Yuanyuan, Koko, Mahmoud, Gjerulfsen, Cathrine E, Sonnenberg, Lukas, Schubert, Julian, Fenger, Christina D, Eltokhi, Ahmed, Rannap, Maert, Koch, Nils A, Lauxmann, Stephan, Krüger, Johanna, Kegele, Josua, Canafoglia, Laura, Franceschetti, Silvana, Mayer, Thomas, Rebstock, Johannes, Zacher, Pia, Ruf, Susanne, Alber, Michael, Sterbova, Katalin, Lassuthová, Petra, Vlckova, Marketa, Lemke, Johannes R, Platzer, Konrad, Krey, Ilona, Heine, Constanze, Wieczorek, Dagmar, Kroell-Seger, Judith, Lund, Caroline, Klein, Karl Martin, Au, P Y Billie, Rho, Jong M, Ho, Alice W, Masnada, Silvia, Veggiotti, Pierangelo, Giordano, Lucio, Accorsi, Patrizia, Hoei-Hansen, Christina E, Striano, Pasquale, Zara, Federico, Verhelst, Helene, Verhoeven, Judith S, Braakman, Hilde M H, van der Zwaag, Bert, Harder, Aster V E, Brilstra, Eva, Pendziwiat, Manuela, Lebon, Sebastian, Vaccarezza, Maria, Le, Ngoc Minh, Christensen, Jakob, Grønborg, Sabine, Scherer, Stephen W, Howe, Jennifer, Fazeli, Walid, Howell, Katherine B, Leventer, Richard, Stutterd, Chloe, Walsh, Sonja, Gerard, Marion, Gerard, Bénédicte, Matricardi, Sara, Bonardi, Claudia M, Sartori, Stefano, Berger, Andrea, Hoffman-Zacharska, Dorota, Mastrangelo, Massimo, Darra, Francesca, Vøllo, Arve, Motazacker, M Mahdi, Lakeman, Phillis, Nizon, Mathilde, Betzler, Cornelia, Altuzarra, Cecilia, Caume, Roseline, Roubertie, Agathe, Gélisse, Philippe, Marini, Carla, Guerrini, Renzo, Bilan, Frederic, Tibussek, Daniel, Koch-Hogrebe, Margarete, Perry, M Scott, Ichikawa, Shoji, Dadali, Elena, Sharkov, Artem, Mishina, Irina, Abramov, Mikhail, Kanivets, Ilya, Korostelev, Sergey, Kutsev, Sergey, Wain, Karen E, Eisenhauer, Nancy, Wagner, Monisa, Savatt, Juliann M, Müller-Schlüter, Karen, Bassan, Haim, Borovikov, Artem, Nassogne, Marie Cecile
Published in Brain (London, England : 1878) (14.09.2022)
Published in Brain (London, England : 1878) (14.09.2022)
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Published in Epilepsia (Copenhagen) (01.02.2018)
Published in Epilepsia (Copenhagen) (01.02.2018)
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De novo variants in KCNA3 cause developmental and epileptic encephalopathy
Soldovieri, Maria Virginia, Ambrosino, Paolo, Mosca, Ilaria, Servettini, Ilenio, Pietrunti, Francesca, Belperio, Giorgio, Syrbe, Steffen, Taglialatela, Maurizio, Lemke, Johannes R
Published in Annals of neurology (01.02.2024)
Published in Annals of neurology (01.02.2024)
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NEXMIF encephalopathy: an X-linked disorder with male and female phenotypic patterns
Stamberger, Hannah, Hammer, Trine B., Gardella, Elena, Vlaskamp, Danique R. M., Bertelsen, Birgitte, Mandelstam, Simone, de Lange, Iris, Zhang, Jing, Myers, Candace T., Fenger, Christina, Afawi, Zaid, Almanza Fuerte, Edith P., Andrade, Danielle M., Balcik, Yunus, Ben Zeev, Bruria, Bennett, Mark F., Berkovic, Samuel F., Isidor, Bertrand, Bouman, Arjan, Brilstra, Eva, Busk, Øyvind L., Cairns, Anita, Caumes, Roseline, Chatron, Nicolas, Dale, Russell C., de Geus, Christa, Edery, Patrick, Gill, Deepak, Granild-Jensen, Jacob Bie, Gunderson, Lauren, Gunning, Boudewijn, Heimer, Gali, Helle, Johan R., Hildebrand, Michael S., Hollingsworth, Georgie, Kharytonov, Volodymyr, Klee, Eric W., Koeleman, Bobby P. C., Koolen, David A., Korff, Christian, Küry, Sébastien, Lesca, Gaetan, Lev, Dorit, Leventer, Richard J., Mackay, Mark T., Macke, Erica L., McEntagart, Meriel, Mohammad, Shekeeb S., Monin, Pauline, Montomoli, Martino, Morava, Eva, Moutton, Sebastien, Muir, Alison M., Parrini, Elena, Procopis, Peter, Ranza, Emmanuelle, Reed, Laura, Reif, Philipp S., Rosenow, Felix, Rossi, Massimiliano, Sadleir, Lynette G., Sadoway, Tara, Schelhaas, Helenius J., Schneider, Amy L., Shah, Krati, Shalev, Ruth, Sisodiya, Sanjay M., Smol, Thomas, Stumpel, Connie T. R. M., Stuurman, Kyra, Symonds, Joseph D., Mau-Them, Frederic Tran, Verbeek, Nienke, Verhoeven, Judith S., Wallace, Geoffrey, Yosovich, Keren, Zarate, Yuri A., Zerem, Ayelet, Zuberi, Sameer M., Guerrini, Renzo, Mefford, Heather C., Patel, Chirag, Zhang, Yue-Hua, Møller, Rikke S., Scheffer, Ingrid E.
Published in Genetics in medicine (01.02.2021)
Published in Genetics in medicine (01.02.2021)
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SLC13A5 is the second gene associated with Kohlschütter–Tönz syndrome
Schossig, Anna, Bloch-Zupan, Agnès, Lussi, Adrian, Wolf, Nicole I, Raskin, Salmo, Cohen, Monika, Giuliano, Fabienne, Jurgens, Julie, Krabichler, Birgit, Koolen, David A, de Macena Sobreira, Nara Lygia, Maurer, Elisabeth, Muller-Bolla, Michèle, Penzien, Johann, Zschocke, Johannes, Kapferer-Seebacher, Ines
Published in Journal of medical genetics (01.01.2017)
Published in Journal of medical genetics (01.01.2017)
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