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Molecular and Phenotypic Characterization of the RORB -Related Disorder

Neurology, 2024-01, Vol.102 (2), p.e207945

2024

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Spectrum of SCN1A gene mutations associated with Dravet syndrome: analysis of 333 patients

Journal of medical genetics, 2009-03, Vol.46 (3), p.183-191

2009

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Resective surgery in tuberous Sclerosis complex, from Penfield to 2018: A critical review

Revue neurologique, 2019-03, Vol.175 (3), p.163-182

2019

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Is the underlying cause of epilepsy a major prognostic factor for recurrence?

Neurology, 1998-11, Vol.51 (5), p.1256-1262

1998

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STAG2 microduplication in a patient with eyelid myoclonia and absences and a review of EMA-related reported genes

European journal of medical genetics, 2022-12, Vol.65 (12), p.104636-104636, Article 104636

2022

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Role of observational studies in supporting extrapolation of efficacy data from adults to children with epilepsy — A systematic review of the literature using lacosamide as an example

European journal of paediatric neurology, 2019-07, Vol.23 (4), p.589-603

2019

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Caveats and pitfalls of “enduring value” publications: Is only the first author responsible?

Epilepsy & behavior, 2013-09, Vol.28 (3), p.533-534

Arzimanoglou, Alexis

2013

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Sturge-Weber syndrome: indications and results of surgery in 20 patients

Neurology, 2000-11, Vol.55 (10), p.1472-1479

2000

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GRIN2A-related disorders: genotype and functional consequence predict phenotype

Brain (London, England : 1878), 2019-01, Vol.142 (1), p.80-92

2019

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INV19 Does early treatment affect epilepsy prognosis?

European journal of paediatric neurology, 2007, Vol.11, p.13-13

Arzimanoglou, A

2007

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Distinct neurological disorders with ATP1A3 mutations

Lancet neurology, 2014-05, Vol.13 (5), p.503-514

2014

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Neuropsychological and behavioral disorders screening program in new-onset childhood epilepsies. Preliminary results using child behavior checklist evaluation

European journal of paediatric neurology, 2017-06, Vol.21, p.e107-e107

2017

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RUFIPRAT: A retrospective study on the everyday clinical use of Rufinamide in children with refractory epilepsy

European journal of paediatric neurology, 2017-06, Vol.21, p.e40-e40

2017

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ATP1A3 screening in patients with alternating hemiplegia of childhood and related phenotypes

European journal of paediatric neurology, 2017-06, Vol.21, p.e162-e162

2017

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Effects of regular auditory or auditory-visual prime sequence on the syntax treatment in childhood absence epilepsy

European journal of paediatric neurology, 2017-06, Vol.21, p.e106-e106

2017

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ILAE Official Report: A practical clinical definition of epilepsy

Epilepsia (Copenhagen), 2014-04, Vol.55 (4), p.475-482

2014

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Prolonged convulsive seizures in children: how are they managed outside the hospital?

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2014-11, Vol.21 (11), p.1252-1261

2014

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Role of valproate across the ages. Treatment of epilepsy in children

Acta neurologica Scandinavica, 2006-08, Vol.114 (s184), p.1-13

2006

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Is Aicardi Syndrome truly linked to a mutation on X-Chromosome?

European journal of paediatric neurology, 2017-06, Vol.21, p.e61-e61

2017

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De novo mutations in ATP1A3 cause alternating hemiplegia of childhood

Nature genetics, 2012-09, Vol.44 (9), p.1030-1034

2012

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Next-generation sequencing allows a diagnostic yield of 23.7% in monogenic epilepsies

European journal of paediatric neurology, 2017-06, Vol.21, p.e168-e169

2017

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Survenue d’une crise d’épilepsie prolongée chez l’enfant : quelle prise en charge en dehors du milieu hospitalier ?

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2014-11, Vol.21 (11), p.1252-1261

2014

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Evidence of a non-progressive course of alternating hemiplegia of childhood: study of a large cohort of children and adults

Brain (London, England : 1878), 2010-12, Vol.133 (12), p.3598-3610

2010

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Timing of antiepileptic drug withdrawal and long-term seizure outcome after paediatric epilepsy surgery (TimeToStop): a retrospective observational study

Lancet neurology, 2012-09, Vol.11 (9), p.784-791

2012

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Intelligence quotient improves after antiepileptic drug withdrawal following pediatric epilepsy surgery

Annals of neurology, 2015-07, Vol.78 (1), p.104-114

2015

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Molecular and Phenotypic Characterization of the RORB -Related Disorder

Spectrum of SCN1A gene mutations associated with Dravet syndrome: analysis of 333 patients

Resective surgery in tuberous Sclerosis complex, from Penfield to 2018: A critical review

Is the underlying cause of epilepsy a major prognostic factor for recurrence?

STAG2 microduplication in a patient with eyelid myoclonia and absences and a review of EMA-related reported genes

Role of observational studies in supporting extrapolation of efficacy data from adults to children with epilepsy — A systematic review of the literature using lacosamide as an example

Caveats and pitfalls of “enduring value” publications: Is only the first author responsible?

Sturge-Weber syndrome: indications and results of surgery in 20 patients

GRIN2A-related disorders: genotype and functional consequence predict phenotype

INV19 Does early treatment affect epilepsy prognosis?

Distinct neurological disorders with ATP1A3 mutations

Neuropsychological and behavioral disorders screening program in new-onset childhood epilepsies. Preliminary results using child behavior checklist evaluation

RUFIPRAT: A retrospective study on the everyday clinical use of Rufinamide in children with refractory epilepsy

ATP1A3 screening in patients with alternating hemiplegia of childhood and related phenotypes

Effects of regular auditory or auditory-visual prime sequence on the syntax treatment in childhood absence epilepsy

ILAE Official Report: A practical clinical definition of epilepsy

Prolonged convulsive seizures in children: how are they managed outside the hospital?

Role of valproate across the ages. Treatment of epilepsy in children

Is Aicardi Syndrome truly linked to a mutation on X-Chromosome?

De novo mutations in ATP1A3 cause alternating hemiplegia of childhood

Next-generation sequencing allows a diagnostic yield of 23.7% in monogenic epilepsies

Survenue d’une crise d’épilepsie prolongée chez l’enfant : quelle prise en charge en dehors du milieu hospitalier ?

Evidence of a non-progressive course of alternating hemiplegia of childhood: study of a large cohort of children and adults

Timing of antiepileptic drug withdrawal and long-term seizure outcome after paediatric epilepsy surgery (TimeToStop): a retrospective observational study

Intelligence quotient improves after antiepileptic drug withdrawal following pediatric epilepsy surgery

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