Is it juvenile myoclonic epilepsy?P Gelisse
Centre Saint Paul, Marseille, France
Epileptic Disord 2:27-32. 2000
..In our opinion, JME can be diagnosed in very uncommon settings, including patients with significant brain damage, as long as all the other criteria for the diagnosis are present...
Dravet syndrome: the long-term outcomePierre Genton
Centre Saint Paul Hôpital Henri Gastaut, Marseille, France
Epilepsia 52:44-9. 2011
..Dependency in adulthood is nearly constant: Only 3 of our 24 adult patients lived independently...
Tiagabine in clinical practiceP Genton
Centre Saint Paul, 13258 Marseille 09, France
Epilepsia 42:42-5. 2001
..Particularly beneficial indications for TGB and/or AED associations including TGB have not been pointed out, but there is a hint that it works best in temporal lobe epilepsies...
Premature death in juvenile myoclonic epilepsyP Genton
Centre Saint Paul H Gastaut, 300 Bd de Sainte Marguerite, 13258 Marseille 09, France
Acta Neurol Scand 104:125-9. 2001
..To report three cases of premature death in juvenile myoclonic epilepsy (JME), a benign form of idiopathic generalized epilepsy (IGE) in which no case of epilepsy-related death has been reported...
[The definition of drug resistance: an epileptologist's perspective]P Genton
Centre Saint Paul, HGG, 300 Boulevard de Sainte Marguerite, 13009 Marseille, France
Rev Neurol (Paris) 160:5S53-9. 2004
....
Progress in pharmaceutical development presentation with improved pharmacokinetics: a new formulation for valproateP Genton
Centre Saint Paul, Marseille, France
Acta Neurol Scand Suppl 182:26-32. 2005
..A stick pack presentation allows individualized dosing and greater convenience...
Valproic acid in epilepsy : pregnancy-related issuesPierre Genton
Centre Saint Paul, Hôpital Gastaut, Marseille, France
Drug Saf 29:1-21. 2006
..Future research on valproic acid and pregnancy should involve risk assessment in large, population-based prospective studies...
Levetiracetam in a broad population of patients with refractory epilepsy: interim results of the international SKATE trialP Genton
Hôpital Henri Gastaut Centre Saint Paul, Marseille, France
Acta Neurol Scand 113:387-94. 2006
..To prospectively assess the safety and efficacy of levetiracetam in patients with uncontrolled focal epilepsy, in a common practice-based setting...
[Unverricht-Lundborg disease (PME1)]P Genton
Centre Saint Paul H Gastaut, Marseille
Rev Neurol (Paris) 162:819-26. 2006
..Clinicians and patients are still waiting for an etiologically oriented treatment, which should, ideally, be admnistered early in the course of the disease, if possible before the onset of invalidating symptoms...
Epilepsy with myoclonic absencesPierre Genton
Centre Saint Paul, Hôpital Henri Gastaut, Marseille, France
CNS Drugs 20:911-6. 2006
..The more benign cases usually present with MA as the only seizure type, while patients who experience other seizures, especially generalised tonic-clonic seizures, in association with MA may have a less favourable outcome...
[Lafora's disease (EPM2)]P Genton
Centre Saint Paul H Gastaut, Marseille
Rev Neurol (Paris) 163:47-53. 2007
..The treatment of LD remains purely symptomatic. Drugs that may aggravate myoclonus must be avoided. Psychological and social management is of utmost importance in LD. Death occurs 4 to 10 years after onset in typical forms...
Absence status epilepsy: delineation of a distinct idiopathic generalized epilepsy syndromePierre Genton
Centre Saint Paul, Hôpital Henri Gastaut, Marseille, France
Epilepsia 49:642-9. 2008
..Absence status epilepticus (AS) is a prolonged, generalized, and nonconvulsive seizure that may occur in various circumstances. We report a series of patients in whom recurrent, unprovoked, typical AS was the main clinical feature...
On the association between valproate and polycystic ovary syndromeP Genton
Centre Saint Paul, Marseille, France
Epilepsia 42:295-304. 2001
..To date, there is no reason to contraindicate the use of VPA in women with epilepsy. However, patients should be informed about the risk of weight gain and its consequences...
[Psychiatric disorders in juvenile myoclonic epilepsy]P Gelisse
Centre Saint Paul, Marseille, France
Rev Neurol (Paris) 157:297-302. 2001
..The presence of PD does not exclude the diagnosis of JME, and PD may represent a further challenge in the comprehensive care of these patients...
Do carbamazepine and phenytoin aggravate juvenile myoclonic epilepsy?P Genton
Centre Saint Paul, Marseille, France
Neurology 55:1106-9. 2000
..However, juvenile myoclonic epilepsy is often misdiagnosed, and some drugs, especially carbamazepine and phenytoin, may have an aggravating effect...
Antimyoclonic effect of levetiracetamP Genton
Centre Saint Paul, 300, boulevard Saint Marguerite, 13009 Marseille, France
Epileptic Disord 2:209-12. 2000
..These preliminary findings suggest that LEV may have interesting antimyoclonic properties that deserve further investigation...
[Benign epilepsy in children and adolescents]P Genton
Centre Saint Paul, Marseille
Presse Med 28:1385-91. 1999
..The appropriate therapeutic attitude is usually abstention from long-term antiepileptic treatment. It is importance for all clinicians to be familiar with "benign" epilepsy...
When antiepileptic drugs aggravate epilepsyP Genton
Centre Saint Paul, 13258, Marseille, France
Brain Dev 22:75-80. 2000
..Patients are usually aware of aggravation before their doctors: we should listen carefully whenever they express a 'dislike' for an AED...
Piracetam and levetiracetam: close structural similarities but different pharmacological and clinical profilesP Genton
Centre Saint Paul, Marseille, France
Epileptic Disord 2:99-105. 2000
..LEV is an antiepileptic drug. Clinical trials have confirmed its efficacy in partial seizures and preliminary findings suggest that it is also effective in generalized seizures and myoclonus...
[Use of topiramate in clinical practice (part 2). Multicentric retrospective evaluation of its safety]P Genton
Centre St Paul, 300 Bd Ste Marguerite, 13258 Marseille cedex 9
Rev Neurol (Paris) 156:1120-5. 2000
..1p.100) or by a combination of these (5p.100). It is useful to use slow titration, in order to allow the greatest possible number of patients to benefit from its efficacy as an add-on drug in the treatment of resistant focal epilepsies...
Are there generalised spike waves and typical absences in benign rolandic epilepsy?P Gelisse
Centre Saint Paul, Marseilles, France
Brain Dev 21:390-6. 1999
..Brief bursts of bilateral abnormalities occur in about 25% of the cases, mostly with sleepiness. Such findings do not substantiate the existence of a continuum between CAE and BECTS...
Incidence of drug-induced aggravation in benign epilepsy with centrotemporal spikesD Corda
Centre Saint Paul, 13258 Marseille 09, France
Epilepsia 42:754-9. 2001
..There is a minor risk of aggravation with CBZ and also probably with PB. Drug-induced aggravation may occur only during certain periods coinciding with spontaneous worsening of BECTS...
Clinical factors of drug resistance in juvenile myoclonic epilepsyP Gelisse
Centre Saint Paul, 300 Bd de Sainte Marguerite, 13009 Marseille, France
J Neurol Neurosurg Psychiatry 70:240-3. 2001
..There is thus a significant subgroup of patients with juvenile myoclonic epilepsy who pose difficult therapeutic problems, and the prevalence of resistant cases may be increased in the experience of a referral epilepsy centre...
Startle response: epileptic or non-epileptic? The case for "flash" SMA reflex seizuresO Cokar
Centre Saint Paul, 13258 Marseille 09, France
Epileptic Disord 3:7-12. 2001
..We concluded that the patient had an unusual form of cryptogenic focal epilepsy originating from the supplementary motor area, presenting as strictly stimulus-triggered "flash" seizures...
Continuous focal spikes during REM sleep in a case of acquired aphasia (Landau-Kleffner syndrome)P Genton
Centre Saint Paul, Marseille, France
Sleep 15:454-60. 1992
..However, this profile was transient and all epileptiform changes disappeared during clinical recovery at 18 months of follow-up...
Severe epilepsy, retardation, and dysmorphic features with a 2q deletion including SCN1A and SCN2AS Pereira
INSERM U491, Marseille, France
Neurology 63:191-2. 2004
[GEFS + syndrome: phenotypic variations from the newborn to the adult in a large French pedigree]F Audic-Gerard
INSERM U491, , Marseille, France
Rev Neurol (Paris) 159:189-95. 2003
..No patient had temporal lobe seizures; they did not have myoclonias nor typical absences. The seizure profile in this family appears to be original, and the existence of yet another type of underlying genetic defect can be suspected...
The Ramsay Hunt syndrome revisited: Mediterranean myoclonus versus mitochondrial encephalomyopathy with ragged-red fibers and Baltic myoclonusP Genton
Centre Saint Paul, Marseille, France
Acta Neurol Scand 81:8-15. 1990
..The authors propose that this form of PME, formerly reported as RHS, be more properly described as Mediterranean myoclonus...
Phenotype variability in a caucasian family with dentatorubral-pallidoluysian atrophyW Casseron
Centre St. Paul, , Marseille, France
Eur Neurol 52:175-6. 2004