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De novo mutations in ATP1A3 cause alternating hemiplegia of childhoodFaulty cardiac repolarization reserve in alternating hemiplegia of childhood broadens the phenotypeHypothalamic hamartoma and epilepsy in children: illustrative cases of possible evolutions.Vagus nerve stimulation for drug-resistant epilepsy: a European long-term study up to 24 months in 347 children.Distinct neurological disorders with ATP1A3 mutationsTreatment of pediatric epilepsy: European expert opinion, 2007.Definition of drug resistant epilepsy: consensus proposal by the ad hoc Task Force of the ILAE Commission on Therapeutic Strategies.Outcome and prognosis of status epilepticus in children.Therapeutic approach to epileptic encephalopathies.Extrapolating evidence of antiepileptic drug efficacy in adults to children ≥2 years of age with focal seizures: The case for disease similarity.Treatment issues for children with epilepsy transitioning to adult care.A subset of genomic alterations detected in rolandic epilepsies contains candidate or known epilepsy genes including GRIN2A and PRRT2.Safety of levetiracetam among infants younger than 12 months--Results from a European multicenter observational study.Cost-effectiveness analysis of epilepsy surgery in a controlled cohort of adult patients with intractable partial epilepsy: A 5-year follow-up study.The administration of rescue medication to children with prolonged acute convulsive seizures in a non-hospital setting: an exploratory survey of healthcare professionals' perspectives.Expert Opinion on the Management of Lennox-Gastaut Syndrome: Treatment Algorithms and Practical Considerations.The outcome of childhood epilepsy: what improvements are needed?A novel three base-pair LGI1 deletion leading to loss of function in a family with autosomal dominant lateral temporal epilepsy and migraine-like episodes.How long for epilepsy remission in the ILAE definition?Behavioral and fMRI responses to fearful faces are altered in benign childhood epilepsy with centrotemporal spikes (BCECTS).Histopathological Findings in Brain Tissue Obtained during Epilepsy Surgery.The role of EEG in the diagnosis and classification of the epilepsy syndromes: a tool for clinical practice by the ILAE Neurophysiology Task Force (Part 1).ADHD in childhood epilepsy: Clinical determinants of severity and of the response to methylphenidate.Functional connectivity of insular efferences.Movement disorders in children: The need to observe, describe in detail and integrate your findings to the global clinical picture.[Medicoeconomic assessment of epilepsy surgery in adults with medically intractable partial epilepsy. Three-year outcomes from a multicenter French cohort].A Review of the New Antiepileptic Drugs for Focal-Onset Seizures in Pediatrics: Role of Extrapolation.MECP2 mutations account for most cases of typical forms of Rett syndrome.Evaluation of long-term safety, tolerability, and behavioral outcomes with adjunctive rufinamide in pediatric patients (≥1 to <4 years old) with Lennox-Gastaut syndrome: Final results from randomized study 303Why the TimeToStop trial failed to recruit: a survey on antiepileptic drug withdrawal after paediatric epilepsy surgeryFrameless robot-assisted stereoelectroencephalography for refractory epilepsy in pediatric patients: accuracy, usefulness, and technical issuesParental mosaicism can cause recurrent transmission ofSCN1A mutations associated with severe myoclonic epilepsy of infancy[Prolonged convulsive seizures in children: how are they managed outside the hospital?]European trends in epilepsy surgeryEpilepsy and cannabidiol: a guide to treatmentEpilepsy surgery near or in eloquent cortex in children-Practice patterns and recommendations for minimizing and reporting deficitsIdentifying the educational needs of physicians in pediatric epilepsy in order to improve care: results from a needs assessment in Germany, Spain, and the United StatesNeonatal tremor episodes and hyperekplexia-like presentation at onset in a child with SCN8A developmental and epileptic encephalopathyElectrical status epilepticus in sleep, a constitutive feature of Christianson syndrome?Predictive factors and prognostic value for status epilepticus in newborns
P50
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P50
description
researcher ORCID ID = 0000-0002-7233-2771
@en
wetenschapper
@nl
name
Alexis Arzimanoglou
@ast
Alexis Arzimanoglou
@en
Alexis Arzimanoglou
@es
Alexis Arzimanoglou
@nl
type
label
Alexis Arzimanoglou
@ast
Alexis Arzimanoglou
@en
Alexis Arzimanoglou
@es
Alexis Arzimanoglou
@nl
prefLabel
Alexis Arzimanoglou
@ast
Alexis Arzimanoglou
@en
Alexis Arzimanoglou
@es
Alexis Arzimanoglou
@nl
P214
P214
P31
P496
0000-0002-7233-2771
P7859
lccn-n2003129184