Successful use of fenfluramine as an add-on treatment for Dravet syndrome von Ceulemans, Berten, Boel, Marc, Leyssens, Katrien, Van Rossem, Carolin, Neels, Pieter, Jorens, Philippe G., Lagae, Lieven

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Therapeutic drug monitoring of fenfluramine in clinical practice: Pharmacokinetic variability and impact of concomitant antiseizure medications von Schoonjans, An‐Sofie, Roosens, Laurence, Dewals, Wendy, Paelinck, Bernard P., Ceulemans, Berten

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Developmental unilateral facial palsy in a newborn: six cases and literature review von Decraene, Laura, Boudewyns, An, Venstermans, Caroline, Ceulemans, Berten

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KCNQ2 encephalopathy: Emerging phenotype of a neonatal epileptic encephalopathy von Weckhuysen, Sarah, Mandelstam, Simone, Suls, Arvid, Audenaert, Dominique, Deconinck, Tine, Claes, Lieve R.F., Deprez, Liesbet, Smets, Katrien, Hristova, Dimitrina, Yordanova, Iglika, Jordanova, Albena, Ceulemans, Berten, Jansen, An, Hasaerts, Danièle, Roelens, Filip, Lagae, Lieven, Yendle, Simone, Stanley, Thorsten, Heron, Sarah E., Mulley, John C., Berkovic, Samuel F., Scheffer, Ingrid E., Peter de Jonghe

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Aberrant Inclusion of a Poison Exon Causes Dravet Syndrome and Related SCN1A-Associated Genetic Epilepsies von 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, Striano, Pasquale, Zara, Federico, Helbig, Ingo, Møller, Rikke S., von Spiczak, Sarah, Muhle, Hiltrud, Caglayan, Hande, Sterbova, Katalin, Craiu, Dana, Hoffman, Dorota, Lehesjoki, Anna-Elina, Selmer, Kaja, Depienne, Christel, Lemke, Johannes, Marini, Carla, Guerrini, Renzo, Neubauer, Bernd, Talvik, Tiina, Leguern, Eric, de Jonghe, Peter, Weckhuysen, Sarah, 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.

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Treatment of Focal-Onset Seizures in Children: Should This Be More Etiology-Driven? von Aeby, Alec, Ceulemans, Berten, Lagae, Lieven

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Low-dose fenfluramine in the treatment of neurologic disorders: experience in Dravet syndrome von Schoonjans, An-Sofie, Lagae, Lieven, Ceulemans, Berten

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Fenfluramine in the treatment of Dravet syndrome: Results of a third randomized, placebo-controlled clinical trial von Sullivan, Joseph, Lagae, Lieven, Cross, J Helen, Devinsky, Orrin, Guerrini, Renzo, Knupp, Kelly G, Laux, Linda, Nikanorova, Marina, Polster, Tilman, Talwar, Dinesh, Ceulemans, Berten, Nabbout, Rima, Farfel, Gail M, Galer, Bradley S, Gammaitoni, Arnold R, Lock, Michael, Agarwal, Anupam, Scheffer, Ingrid E

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Pharmacological characterization of an antisense knockdown zebrafish model of Dravet syndrome: inhibition of epileptic seizures by the serotonin agonist fenfluramine von Zhang, Yifan, Kecskés, Angéla, Copmans, Daniëlle, Langlois, Mélanie, Crawford, Alexander D, Ceulemans, Berten, Lagae, Lieven, de Witte, Peter A M, Esguerra, Camila V

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Lessons learned from 40 novel PIGA patients and a review of the literature von Bayat, Allan, Knaus, Alexej, Pendziwiat, Manuela, Afenjar, Alexandra, Barakat, Tahsin Stefan, Bosch, Friedrich, Callewaert, Bert, Calvas, Patrick, Ceulemans, Berten, Chassaing, Nicolas, Depienne, Christel, Endziniene, Milda, Ferreira, Carlos R., Moura de Souza, Carolina Fischinger, Freihuber, Cécile, Ganesan, Shiva, Gataullina, Svetlana, Guerrini, Renzo, Guerrot, Anne‐Marie, Hansen, Lars, Jezela‐Stanek, Aleksandra, Karsenty, Caroline, Kievit, Anneke, Kooy, Frank R., Korff, Christian M., Kragh Hansen, Johanne, Larsen, Martin, Layet, Valérie, Lesca, Gaetan, McBride, Kim L., Meuwissen, Marije, Mignot, Cyril, Montomoli, Martino, Moore, Hannah, Naudion, Sophie, Nava, Caroline, Nougues, Marie‐Christine, Parrini, Elena, Pastore, Matthew, Schelhaas, Jurgen H., Skinner, Steven, Szczałuba, Krzysztoł, Thomas, Ashley, Thomassen, Mads, Tranebjærg, Lisbeth, Slegtenhorst, Marjon, Wolfe, Lynne A., Lal, Dennis, Gardella, Elena, Bomme Ousager, Lilian, Brünger, Tobias, Helbig, Ingo, Krawitz, Peter, Møller, Rikke S.

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Variants in the SK2 channel gene (KCNN2) lead to dominant neurodevelopmental movement disorders von Mochel, Fanny, Rastetter, Agnes, Ceulemans, Berten, Platzer, Konrad, Yang, Sandra, Shinde, Deepali N., Helbig, Katherine L., Lopergolo, Diego, Mari, Francesca, Renieri, Alessandra, Benetti, Elisa, Canitano, Roberto, Waisfisz, Quinten, Plomp, Astrid S., Huisman, Sylvia A., Wilson, Golder N., Cathey, Sara S., Louie, Raymond J., Del Gaudio, Daniela, Waggoner, Darrel, Kacker, Shawn, Nugent, Kimberly M., Roeder, Elizabeth R., Bruel, Ange-Line, Thevenon, Julien, Ehmke, Nadja, Horn, Denise, Holtgrewe, Manuel, Kaiser, Frank J., Kamphausen, Susanne B., Abou Jamra, Rami, Weckhuysen, Sarah, Dalle, Carine, Depienne, Christel

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Early-onset absence epilepsy caused by mutations in the glucose transporter GLUT1 von Suls, Arvid, Mullen, Saul A., Weber, Yvonne G., Verhaert, Kristien, Ceulemans, Berten, Guerrini, Renzo, Wuttke, Thomas V., Salvo-Vargas, Alberto, Deprez, Liesbet, Claes, Lieve R. F., Jordanova, Albena, Berkovic, Samuel F., Lerche, Holger, De Jonghe, Peter, Scheffer, Ingrid E.

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De Novo Mutations in the Sodium-Channel Gene SCN1A Cause Severe Myoclonic Epilepsy of Infancy von Claes, Lieve, Del-Favero, Jurgen, Ceulemans, Berten, Lagae, Lieven, Van Broeckhoven, Christine, De Jonghe, Peter

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Clinical correlations of mutations in the SCN1A gene: from febrile seizures to severe myoclonic epilepsy in infancy von Ceulemans, Berten P.G.M, Claes, Lieve R.F, Lagae, Lieven G

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A randomized double-blind, placebo-controlled trial of ganaxolone in children and adolescents with fragile X syndrome von 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

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Childhood chronic inflammatory demyelinating polyneuroradiculopathy – Three cases and a review of the literature von Riekhoff, Antoinetta G.M, Jadoul, Chris, Mercelis, Rudy, Cras, Patrick, Ceulemans, Berten P.G.M

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Recurrent NEDD4L Variant in Periventricular Nodular Heterotopia, Polymicrogyria and Syndactyly von Stouffs, Katrien, Verloo, Patrick, Brock, Stefanie, Regal, Luc, Beysen, Diane, Ceulemans, Barten, Jansen, Anna C., Meuwissen, Marije E. C.

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Pseudomonas aeruginosa in children with cerebral palsy: a prospective study von Romaen, Katrien, Van Ussel, Isabelle, Van Rossem, Carolin, Kenis, Sandra, Ceulemans, Berten, Van Hoorenbeeck, Kim, Verhulst, Stijn

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Clinical Investigation of French Maritime Pine Bark Extract on Attention-Deficit Hyperactivity Disorder as compared to Methylphenidate and Placebo: Part 1: Efficacy in a Randomised... von Weyns, Anne-Sophie, Verlaet, Annelies A.J., Breynaert, Annelies, Naessens, Tania, Fransen, Erik, Verhelst, Helene, Van West, Dirk, Van Ingelghem, Ingrid, Jonckheere, An I., Beysen, Diane, Kenis, Sandra, Moens, Els, van Roest, Aalt P.J., Savelkoul, Huub F.J., De Bruyne, Tess, Pieters, Luc, Ceulemans, Berten, Hermans, Nina

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Overall management of patients with Dravet syndrome von CEULEMANS, BERTEN

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