نتائج البحث - Ceulemans, Berten
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Long-term accelerometry-triggered video monitoring and detection of tonic–clonic and clonic seizures in a home environment: Pilot study حسب Van de Vel, Anouk, Milosevic, Milica, Bonroy, Bert, Cuppens, Kris, Lagae, Lieven, Vanrumste, Bart, Van Huffel, Sabine, Ceulemans, Berten
منشور في 2016نص -
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Recurrent NEDD4L Variant in Periventricular Nodular Heterotopia, Polymicrogyria and Syndactyly حسب Stouffs, Katrien, Verloo, Patrick, Brock, Stefanie, Régal, Luc, Beysen, Diane, Ceulemans, Berten, Jansen, Anna C., Meuwissen, Marije E.C.
منشور في 2020نص -
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Effect of Pycnogenol® on attention-deficit hyperactivity disorder (ADHD): study protocol for a randomised controlled trial حسب Verlaet, Annelies A. J., Ceulemans, Berten, Verhelst, Helene, Van West, Dirk, De Bruyne, Tess, Pieters, Luc, Savelkoul, Huub F. J., Hermans, Nina
منشور في 2017نص -
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Pharmacological Characterization of an Antisense Knockdown Zebrafish Model of Dravet Syndrome: Inhibition of Epileptic Seizures by the Serotonin Agonist Fenfluramine حسب Zhang, Yifan, Kecskés, Angéla, Copmans, Daniëlle, Langlois, Mélanie, Crawford, Alexander D., Ceulemans, Berten, Lagae, Lieven, de Witte, Peter A. M., Esguerra, Camila V.
منشور في 2015نص -
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Biallelic ADPRHL2 mutations in complex neuropathy affect ADP ribosylation and DNA damage response حسب Beijer, Danique, Agnew, Thomas, Rack, Johannes Gregor Matthias, Prokhorova, Evgeniia, Deconinck, Tine, Ceulemans, Berten, Peric, Stojan, Milic Rasic, Vedrana, De Jonghe, Peter, Ahel, Ivan, Baets, Jonathan
منشور في 2021نص -
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SCN1B‐linked early infantile developmental and epileptic encephalopathy حسب Aeby, Alec, Sculier, Claudine, Bouza, Alexandra A., Askar, Brandon, Lederer, Damien, Schoonjans, Anne‐Sofie, Vander Ghinst, Marc, Ceulemans, Berten, Offord, James, Lopez‐Santiago, Luis F., Isom, Lori L.
منشور في 2019نص -
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A randomized double-blind, placebo-controlled trial of ganaxolone in children and adolescents with fragile X syndrome حسب Ligsay, Andrew, Van Dijck, Anke, Nguyen, Danh V., Lozano, Reymundo, Chen, Yanjun, Bickel, Erika S., Hessl, David, Schneider, Andrea, Angkustsiri, Kathleen, Tassone, Flora, Ceulemans, Berten, Kooy, R. Frank, Hagerman, Randi J.
منشور في 2017نص -
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Novel Infantile-Onset Leukoencephalopathy With High Lactate Level and Slow Improvement حسب Steenweg, Marjan E., Vanderver, Adeline, Ceulemans, Berten, Prabhakar, Prab, Régal, Luc, Fattal-Valevski, Aviva, Richer, Lawrence, Simonetti, Barbara Goeggel, Barkhof, Frederik, Rodenburg, Richard J. T., Pouwels, Petra J. W., van der Knaap, Marjo S.
منشور في 2012نص -
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First de novo KCND3 mutation causes severe Kv4.3 channel dysfunction leading to early onset cerebellar ataxia, intellectual disability, oral apraxia and epilepsy حسب Smets, Katrien, Duarri, Anna, Deconinck, Tine, Ceulemans, Berten, van de Warrenburg, Bart P., Züchner, Stephan, Gonzalez, Michael Anthony, Schüle, Rebecca, Synofzik, Matthis, Van der Aa, Nathalie, De Jonghe, Peter, Verbeek, Dineke S., Baets, Jonathan
منشور في 2015نص -
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Two male adults with pathogenic AUTS2 variants, including a two-base pair deletion, further delineate the AUTS2 syndrome حسب Beunders, Gea, de Munnik, Sonja A, Van der Aa, Nathalie, Ceulemans, Berten, Voorhoeve, Els, Groffen, Alexander J, Nillesen, Willy M, Meijers-Heijboer, Elizabeth J, Frank Kooy, R, Yntema, Helger G, Sistermans, Erik A
منشور في 2015نص -
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Efficacy and Safety of Fenfluramine for the Treatment of Seizures Associated With Lennox-Gastaut Syndrome: A Randomized Clinical Trial حسب Knupp, Kelly G., Scheffer, Ingrid E., Ceulemans, Berten, Sullivan, Joseph E., Nickels, Katherine C., Lagae, Lieven, Guerrini, Renzo, Zuberi, Sameer M., Nabbout, Rima, Riney, Kate, Shore, Svetlana, Agarwal, Anupam, Lock, Michael, Farfel, Gail M., Galer, Bradley S., Gammaitoni, Arnold R., Davis, Ronald, Gil-Nagel, Antonio
منشور في 2022نص -
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Development and Validation of a Prediction Model for Early Diagnosis of SCN1A-Related Epilepsies حسب Brunklaus, Andreas, Pérez-Palma, Eduardo, Ghanty, Ismael, Xinge, Ji, Brilstra, Eva, Ceulemans, Berten, Chemaly, Nicole, de Lange, Iris, Depienne, Christel, Guerrini, Renzo, Mei, Davide, Møller, Rikke S., Nabbout, Rima, Regan, Brigid M., Schneider, Amy L., Scheffer, Ingrid E., Schoonjans, An-Sofie, Symonds, Joseph D., Weckhuysen, Sarah, Kattan, Michael W., Zuberi, Sameer M., Lal, Dennis
منشور في 2022نص -
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Treatment Responsiveness in KCNT1-Related Epilepsy حسب Fitzgerald, Mark P., Fiannacca, Martina, Smith, Douglas M., Gertler, Tracy S., Gunning, Boudewijn, Syrbe, Steffen, Verbeek, Nienke, Stamberger, Hannah, Weckhuysen, Sarah, Ceulemans, Berten, Schoonjans, An-Sofie, Rossi, Massimiliano, Demarquay, Geneviève, Lesca, Gaetan, Olofsson, Kern, Koolen, D. A., Hornemann, Frauke, Baulac, Stephanie, Rubboli, Guido, Minks, Kelly Q., Lee, Bohoon, Helbig, Ingo, Dlugos, Dennis, Møller, Rikke S., Bearden, David
منشور في 2019نص -
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Aberrant Inclusion of a Poison Exon Causes Dravet Syndrome and Related SCN1A-Associated Genetic Epilepsies حسب Carvill, Gemma L., Engel, Krysta L., Ramamurthy, Aishwarya, Cochran, J. Nicholas, Roovers, Jolien, Stamberger, Hannah, Lim, Nicholas, Schneider, Amy L., Hollingsworth, Georgie, Holder, Dylan H., Regan, Brigid M., Lawlor, James, Lagae, Lieven, Ceulemans, Berten, Bebin, E. Martina, Nguyen, John, Barsh, Gregory S., Weckhuysen, Sarah, Meisler, Miriam, Berkovic, Samuel F., De Jonghe, Peter, Scheffer, Ingrid E., Myers, Richard M., Cooper, Gregory M., Mefford, Heather C.
منشور في 2018نص -
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Genetic spectrum of hereditary neuropathies with onset in the first year of life حسب Baets, Jonathan, Deconinck, Tine, De Vriendt, Els, Zimoń, Magdalena, Yperzeele, Laetitia, Van Hoorenbeeck, Kim, Peeters, Kristien, Spiegel, Ronen, Parman, Yesim, Ceulemans, Berten, Van Bogaert, Patrick, Pou-Serradell, Adolf, Bernert, Günther, Dinopoulos, Argirios, Auer-Grumbach, Michaela, Sallinen, Satu-Leena, Fabrizi, Gian Maria, Pauly, Fernand, Van den Bergh, Peter, Bilir, Birdal, Battaloglu, Esra, Madrid, Ricardo E., Kabzińska, Dagmara, Kochanski, Andrzej, Topaloglu, Haluk, Miller, Geoffrey, Jordanova, Albena, Timmerman, Vincent, De Jonghe, Peter
منشور في 2011نص