INTRODUCTION: Despite the fact that more than 20 antiepileptic drugs (AEDs) are currently available, about one-third of patients still present drug resistance. Further efforts are required to develop novel and more efficacious therapeutic strategies, especially for refractory epileptic syndromes showing few and anecdotic therapeutic options. AREAS COVERED: Stiripentol (STP) is a second generation AED that shows GABAergic activity, with immature brain selectivity, and an indirect metabolic action on co-administered AEDs. Two pivotal studies demonstrated STP efficacy in patients with Dravet syndrome with refractory partial seizures, and marketing authorization in Europe, Canada and Japan was granted thereafter. Post-marketing surveys reporte...
New antiepileptic drugs are regularly approved for treatment and offer large therapeutic opportuniti...
The mainstay of therapy for epilepsy is anti-seizure drugs (ASDs, also referred to as anticonvulsant...
Lennox–Gastaut syndrome is a childhood epileptic encephalopathy characterised by polymorphic seizure...
BACKGROUND: Severe myoclonic epilepsy in infants (SMEI), also known as Dravet syndrome, is a rare, r...
BACKGROUND: This is an updated version of the original Cochrane review published in 2014 (Issue 1). ...
AIM: To assess long-term safety and efficacy of stiripentol as an antiepileptic medication for peopl...
International audiencePURPOSE: Stiripentol (STP) is currently an efficient drug for add-on therapy i...
Summary: Purpose: Stiripentol (STP) is currently an efficient drug for add-on therapy in infantile e...
Catherine Chiron1–31INSERM U1129, Paris, France; 2Paris Descartes University, Paris, France; 3...
International audienceDravet syndrome is a highly pharmaco-resistant form of epilepsy. Valproate and...
BACKGROUND: Stiripentol is an antiseizure medication with multiple potential mechanisms of action, i...
Introduction: Epilepsy is a neurological disorder that significantly impacts the quality of life of ...
Introduction: Despite optimal medical treatment, up to 30% of patients with epilepsy continue to exp...
For several decades, both in vitro and in vivo models of seizures and epilepsy have been employed to...
Introduction. One of the most common neurological disorders is epilepsy, characterised by recurrent ...
New antiepileptic drugs are regularly approved for treatment and offer large therapeutic opportuniti...
The mainstay of therapy for epilepsy is anti-seizure drugs (ASDs, also referred to as anticonvulsant...
Lennox–Gastaut syndrome is a childhood epileptic encephalopathy characterised by polymorphic seizure...
BACKGROUND: Severe myoclonic epilepsy in infants (SMEI), also known as Dravet syndrome, is a rare, r...
BACKGROUND: This is an updated version of the original Cochrane review published in 2014 (Issue 1). ...
AIM: To assess long-term safety and efficacy of stiripentol as an antiepileptic medication for peopl...
International audiencePURPOSE: Stiripentol (STP) is currently an efficient drug for add-on therapy i...
Summary: Purpose: Stiripentol (STP) is currently an efficient drug for add-on therapy in infantile e...
Catherine Chiron1–31INSERM U1129, Paris, France; 2Paris Descartes University, Paris, France; 3...
International audienceDravet syndrome is a highly pharmaco-resistant form of epilepsy. Valproate and...
BACKGROUND: Stiripentol is an antiseizure medication with multiple potential mechanisms of action, i...
Introduction: Epilepsy is a neurological disorder that significantly impacts the quality of life of ...
Introduction: Despite optimal medical treatment, up to 30% of patients with epilepsy continue to exp...
For several decades, both in vitro and in vivo models of seizures and epilepsy have been employed to...
Introduction. One of the most common neurological disorders is epilepsy, characterised by recurrent ...
New antiepileptic drugs are regularly approved for treatment and offer large therapeutic opportuniti...
The mainstay of therapy for epilepsy is anti-seizure drugs (ASDs, also referred to as anticonvulsant...
Lennox–Gastaut syndrome is a childhood epileptic encephalopathy characterised by polymorphic seizure...