Catherine Chiron1–31INSERM U1129, Paris, France; 2Paris Descartes University, Paris, France; 3CEA, Gif-sur-Yvette, FranceAbstract: Stiripentol (marketed by Biocodex as Diacomit®) is an anticonvulsant drug, structurally unrelated to any other compound, which has recently been approved as adjunctive therapy with clobazam and valproate for Dravet syndrome in Europe, Canada, and Japan. This rare form of early childhood epilepsy is associated with subsequent cognitive impairment, significant risk of death, and high pharmacoresistance. Based on an efficacy signal of stiripentol added to clobazam and valproate in an observational, prospectively conducted, exploratory study including 10% of children with Dravet syndrome, a randomized plac...
OBJECTIVES: There are very few data available in the literature on the use of stiripentol in adults ...
Objective: Dravet syndrome is a developmental and epileptic encephalopathy characterized by severe a...
Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/100157/1/epi12303.pd
International audienceDravet syndrome is a highly pharmaco-resistant form of epilepsy. Valproate and...
AIM: To assess long-term safety and efficacy of stiripentol as an antiepileptic medication for peopl...
AbstractDravet syndrome is a rare form of epilepsy largely refractory to current antiepileptic medic...
Developmental and epileptic encephalopathies (DEEs) are rare neurodevelopmental disorders characteri...
Introduction: Dravet syndrome (DS), a prototypic developmental and genetic epileptic encephalopathy ...
INTRODUCTION: Despite the fact that more than 20 antiepileptic drugs (AEDs) are currently available,...
Objective Dravet syndrome is a developmental and epileptic encephalopathy characterized by severe an...
BackgroundDravet syndrome (DS) is a severe developmental and epileptic encephalopathy characterized ...
BACKGROUND: Stiripentol is an antiseizure medication with multiple potential mechanisms of action, i...
Introduction: Dravet syndrome (DS) is an early-onset genetic developmental epileptic encephalopathy ...
Importance: Fenfluramine treatment may reduce monthly convulsive seizure frequency in patients with ...
BACKGROUND: Severe myoclonic epilepsy in infants (SMEI), also known as Dravet syndrome, is a rare, r...
OBJECTIVES: There are very few data available in the literature on the use of stiripentol in adults ...
Objective: Dravet syndrome is a developmental and epileptic encephalopathy characterized by severe a...
Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/100157/1/epi12303.pd
International audienceDravet syndrome is a highly pharmaco-resistant form of epilepsy. Valproate and...
AIM: To assess long-term safety and efficacy of stiripentol as an antiepileptic medication for peopl...
AbstractDravet syndrome is a rare form of epilepsy largely refractory to current antiepileptic medic...
Developmental and epileptic encephalopathies (DEEs) are rare neurodevelopmental disorders characteri...
Introduction: Dravet syndrome (DS), a prototypic developmental and genetic epileptic encephalopathy ...
INTRODUCTION: Despite the fact that more than 20 antiepileptic drugs (AEDs) are currently available,...
Objective Dravet syndrome is a developmental and epileptic encephalopathy characterized by severe an...
BackgroundDravet syndrome (DS) is a severe developmental and epileptic encephalopathy characterized ...
BACKGROUND: Stiripentol is an antiseizure medication with multiple potential mechanisms of action, i...
Introduction: Dravet syndrome (DS) is an early-onset genetic developmental epileptic encephalopathy ...
Importance: Fenfluramine treatment may reduce monthly convulsive seizure frequency in patients with ...
BACKGROUND: Severe myoclonic epilepsy in infants (SMEI), also known as Dravet syndrome, is a rare, r...
OBJECTIVES: There are very few data available in the literature on the use of stiripentol in adults ...
Objective: Dravet syndrome is a developmental and epileptic encephalopathy characterized by severe a...
Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/100157/1/epi12303.pd