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Qiong Wu et al.
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Sophie Peigne et al.
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Shane H. Licheni et al.
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Tyler E. Gaston et al.
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Trial of Cannabidiol for Drug-Resistant Seizures in the Dravet Syndrome
Rongrui Tang et al.
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Trial of Cannabidiol for Drug-Resistant Seizures in the Dravet Syndrome
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Elaine C. Wirrell et al.
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Kelly G. Knupp et al.
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Gaetano Zaccara et al.
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Brian P. Grone et al.
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An-Sofie Schoonjans et al.
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Nienke Verbeek et al.
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Clemizole and modulators of serotonin signalling suppress seizures in Dravet syndrome
Aliesha Griffin et al.
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Elaine C. Wirrell
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Brian J. Dlouhy et al.
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Georgios Kosmidis et al.
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Berten Ceulemans et al.
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Disorders of early language development in Dravet syndrome
Daniela Chieffo et al.
EPILEPSY & BEHAVIOR (2016)
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Domenica Battaglia et al.
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Paola De Liso et al.
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Mortality in Dravet syndrome
Monica S. Cooper et al.
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Role for serotonin2A (5-HT2A) and 2C (5-HT2C) receptors in experimental absence seizures
Marcello Venzi et al.
NEUROPHARMACOLOGY (2016)
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Nadeem Siddiqui et al.
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Pitfalls in genetic testing: the story of missed SCN1A mutations
Tania Djemie et al.
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Seizure precipitants in Dravet syndrome: What events and activities are specifically provocative compared with other epilepsies?
Nienke E. Verbeek et al.
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Efficacy and tolerability of the ketogenic diet in Dravet syndrome - Comparison with various standard antiepileptic drug regimen
Anastasia Dressler et al.
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Incidence of Dravet Syndrome in a US Population
Yvonne W. Wu et al.
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Vincent Jullien et al.
CLINICAL PHARMACOKINETICS (2015)
Lamotrigine can be beneficial in patients with Dravet syndrome
Linda Dalic et al.
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Role(s) of the 5-HT2C Receptor in the Development of Maximal Dentate Activation in the Hippocampus of Anesthetized Rats
Gergely Orban et al.
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Andreas Brunklaus et al.
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Alfonso Fasano et al.
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Elaine C. Wirrell et al.
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Rima Nabbout et al.
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Scott C. Baraban et al.
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Progressive Gait Deterioration in Adolescents With Dravet Syndrome
Jill M. Rodda et al.
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Prognostic, clinical and demographic features in SCN1A mutation-positive Dravet syndrome
A. Brunklaus et al.
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Jennifer J. Rilstone et al.
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Successful use of fenfluramine as an add-on treatment for Dravet syndrome
Berten Ceulemans et al.
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Electroencephalographic Features in Dravet Syndrome: Five-Year Follow-Up Study in 22 Patients
Nicola Specchio et al.
JOURNAL OF CHILD NEUROLOGY (2012)
Comorbidities and predictors of health-related quality of life in Dravet syndrome
Andreas Brunklaus et al.
EPILEPSIA (2011)
Ketogenic diet also benefits Dravet syndrome patients receiving stiripentol: A prospective pilot study
Rima Nabbout et al.
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A prospective open-labeled trial with levetiracetam in pediatric epilepsy syndromes: Continuous spikes and waves during sleep is definitely a target
S. Chhun et al.
SEIZURE-EUROPEAN JOURNAL OF EPILEPSY (2011)
Optogenetic Localization and Genetic Perturbation of Saccade-Generating Neurons in Zebrafish
Peter J. Schoonheim et al.
JOURNAL OF NEUROSCIENCE (2010)
Addition of verapamil in the treatment of severe myoclonic epilepsy in infancy
Paola Iannetti et al.
EPILEPSY RESEARCH (2009)
Valvular regurgitation and surgery associated with fenfluramine use: an analysis of 5743 individuals
Charles F. Dahl et al.
BMC MEDICINE (2008)
An open-label trial of levetiracetam in severe myoclonic epilepsy of infancy
P. Striano et al.
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Ellen M. Welch et al.
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Serotonergic 5-HT2C receptors as a potential therapeutic target for the design antiepileptic drugs
M Isaac
CURRENT TOPICS IN MEDICINAL CHEMISTRY (2005)
Clinical correlations of mutations in the SCN1A gene:: From febrile seizures to severe myoclonic epilepsy in infancy
BPGM Ceulemans et al.
PEDIATRIC NEUROLOGY (2004)
Topiramate as add-on drug in severe myoclonic epilepsy in infancy: an Italian multicenter open trial
G Coppola et al.
EPILEPSY RESEARCH (2002)
De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy
L Claes et al.
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Topiramate in the treatment of severe myoclonic epilepsy in infancy
M Nieto-Barrera et al.
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C Chiron et al.
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