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Epilepsia, ISSN 0013-9580, 07/2016, Volume 57, Issue 7, pp. e129 - e134
Journal Article
Epilepsia, ISSN 0013-9580, 10/2018, Volume 59, Issue 10, pp. 1881 - 1888
Summary Objective Lennox‐Gastaut syndrome (LGS) is a drug‐resistant, childhood onset electroclinical epilepsy syndrome with multiple seizure types and... 
phase 2 | childhood epilepsy | seizure frequency | fenfluramine | Lennox‐Gastaut syndrome | ZX008 | Lennox-Gastaut syndrome | DIAGNOSIS | CANNABIDIOL | DRAVET SYNDROME | STIRIPENTOL | CLINICAL NEUROLOGY | TRIAL | IN-VITRO | INHIBITION | SEIZURES | METABOLISM | SEROTONIN | Medical research | Epilepsy | Medicine, Experimental | Fenfluramine | Dosage and administration | Seizures (Medicine) | Drug resistance | Oral medication
Journal Article
by Coppola, Antonietta and Cellini, Elena and Stamberger, Hannah and Saarentaus, Elmo and Cetica, Valentina and Lal, Dennis and Djémié, Tania and Bartnik‐Glaska, Magdalena and Ceulemans, Berten and Helen Cross, J and Deconinck, Tine and Masi, Salvatore De and Dorn, Thomas and Guerrini, Renzo and Hoffman‐Zacharska, Dorotha and Kooy, Frank and Lagae, Lieven and Lench, Nicholas and Lemke, Johannes R and Lucenteforte, Ersilia and Madia, Francesca and Mefford, Heather C and Morrogh, Deborah and Nuernberg, Peter and Palotie, Aarno and Schoonjans, An‐Sofie and Striano, Pasquale and Szczepanik, Elzbieta and Tostevin, Anna and Vermeesch, Joris R and Van Esch, Hilde and Van Paesschen, Wim and Waters, Jonathan J and Weckhuysen, Sarah and Zara, Federico and De Jonghe, Peter and Sisodiya, Sanjay M and Marini, Carla and Lehesjioki, Anna‐Elina and Craiu, Dana and Talvik, Tiina and Caglayan, Hande and Serratosa, Jose and Sterbova, Katalin and Møller, Rikke S and Hjalgrim, Helle and Lerche, Holger and Weber, Yvonne and Helbig, Ingo and Spiczak, Sarah and Barba, Carmen and Bogaerts, Anneleen and Boni, Antonella and Galizia, Elisabeth Caruana and Chiari, Sara and Gacomo, Gianpiero and Ferrari, Annarita and Guarducci, Silvia and Giglio, Sabrina and Holmgren, Philip and Leu, Costin and Melani, Federico and Novara, Francesca and Pantaleo, Marilena and Peeters, Elke and Pisano, Tiziana and Rosati, Anna and Sander, Josemir and Schoeler, Natasha and Stankiewicz, Pawel and Striano, Salvatore and Suls, Arvid and Traverso, Monica and Vandeweyer, Geert and Dijck, Anke and Zuffardi, Orsetta and EpiCNV Consortium and EuroEPINOMICS-RES Consortium and EuroEPINOMICS‐RES Consortium
Epilepsia, ISSN 0013-9580, 04/2019, Volume 60, Issue 4, pp. 689 - 706
Journal Article
Journal Article
by Baldassari, Sara and Picard, Fabienne and Verbeek, Nienke E and van Kempen, Marjan and Brilstra, Eva H and Lesca, Gaetan and Conti, Valerio and Guerrini, Renzo and Bisulli, Francesca and Licchetta, Laura and Pippucci, Tommaso and Tinuper, Paolo and Hirsch, Edouard and de Saint Martin, Anne and Chelly, Jamel and Rudolf, Gabrielle and Chipaux, Mathilde and Ferrand-Sorbets, Sarah and Dorfmüller, Georg and Sisodiya, Sanjay and Balestrini, Simona and Schoeler, Natasha and Hernandez-Hernandez, Laura and Krithika, S and Oegema, Renske and Hagebeuk, Eveline and Gunning, Boudewijn and Deckers, Charles and Berghuis, Bianca and Wegner, Ilse and Niks, Erik and Jansen, Floor E and Braun, Kees and de Jong, Daniëlle and Rubboli, Guido and Talvik, Inga and Sander, Valentin and Uldall, Peter and Jacquemont, Marie Line and Nava, Caroline and Leguern, Eric and Julia, Sophie and Gambardella, Antonio and d’Orsi, Giuseppe and Crichiutti, Giovanni and Faivre, Laurence and Darmency, Veronique and Benova, Barbora and Krsek, Pavel and Biraben, Arnaud and Lebre, Anne Sophie and Jennesson, Mélanie and Sattar, Shifteh and Marchal, Cécile and Nordli, Douglas R and Lindstrom, Kristin and Striano, Pasquale and Lomax, Lysa Boissé and Kiss, Courtney and Bartolomei, Fabrice and Lepine, Anne Fabienne and Schoonjans, An Sofie and Stouffs, Katrien and Jansen, Anna and Panagiotakaki, Eleni and Ricard-Mousnier, Brigitte and Thevenon, Julien and de Bellescize, Julitta and Catenoix, Hélène and Dorn, Thomas and Zenker, Martin and Müller-Schlüter, Karen and Brandt, Christian and Krey, Ilona and Polster, Tilman and Wolff, Markus and Balci, Meral and Rostasy, Kevin and Achaz, Guillaume and Zacher, Pia and Becher, Thomas and Cloppenborg, Thomas and Yuskaitis, Christopher J and Weckhuysen, Sarah and Poduri, Annapurna and Lemke, Johannes R and Møller, Rikke S and Baulac, Stéphanie
Genetics in medicine, ISSN 1098-3600, 02/2019, Volume 21, Issue 2, pp. 398 - 408
Journal Article
11/2015, Volume 8, Issue 6, 11
In this paper, we review the experience with fenfluramine in epileptic and other paroxysmal disorders. Since the best available data are from the treatment of... 
serotonin | childhood epilepsy | drug resistance | fenfluramine | Dravet | SCN1A | BRAIN-SEROTONIN | VALVULAR HEART-DISEASE | FEBRILE SEIZURES | ELECTROENCEPHALOGRAPHIC FEATURES | ANTIDEPRESSANT DRUGS | CLINICAL NEUROLOGY | SCN1A MUTATIONS | 5-HT RECEPTORS | SEROTONIN DEPLETION | SEVERE MYOCLONIC EPILEPSY | ANTIEPILEPTIC DRUG | Reviews
Book Review
European Journal of Paediatric Neurology, ISSN 1090-3798, 01/2019, Volume 23, Issue 1, pp. 61 - 69
Sleep problems are often reported in patients with a Dravet Syndrome (DS). In this study we explored the sleep behavior in DS and compared the prevalence of... 
Sleep disorder | Dravet Syndrome | Epilepsy | Sleep behavior | SQ-SP questionnaire | BEHAVIOR | DISORDERS | CLINICAL NEUROLOGY | CHILDREN | INDIVIDUALS | IMPACT | COMORBIDITIES | MOUSE MODEL | PEDIATRICS | QUESTIONNAIRE | LIFE | Prevalence | Sleep Wake Disorders - epidemiology | Humans | Female | Male | Surveys and Questionnaires | Child | Sleep Wake Disorders - etiology | Sleepiness | Epilepsies, Myoclonic - complications
Journal Article
Journal of Medical Genetics, ISSN 0022-2593, 09/2017, Volume 54, Issue 9, pp. 613 - 623
Journal Article
Journal Article
European Journal of Paediatric Neurology, ISSN 1090-3798, 2016, Volume 20, Issue 3, pp. 474 - 479
Journal Article
Clinical Pharmacology & Therapeutics, ISSN 0009-9236, 11/2019, Volume 106, Issue 5, pp. 929 - 932
Journal Article
Journal of Neurology, Neurosurgery & Psychiatry, ISSN 0022-3050, 04/2014, Volume 85, Issue 4, pp. 462 - 465
Journal Article
Developmental Medicine & Child Neurology, ISSN 0012-1622, 08/2019, Volume 61, Issue 8, pp. 950 - 956
Aim The aim of this study is to describe the course of motor development in children with Dravet syndrome. Method Forty‐three participants (21 males, 22... 
PHENOTYPE | PEDIATRICS | SEVERE MYOCLONIC EPILEPSY | COGNITIVE-DEVELOPMENT | EPIDEMIOLOGY | CLINICAL NEUROLOGY | FEATURES
Journal Article