Alexis Arzimanoglou

Research interests

Publications

• The gain of function SCN1A disorder spectrum: novel epilepsy phenotypes and therapeutic implications

  Brain · 2022 · https://doi.org/10.1093/brain/awac210

• Seizure outcome and use of antiepileptic drugs after epilepsy surgery according to histopathological diagnosis: a retrospective multicentre cohort study

  The Lancet Neurology · 2020 · https://doi.org/10.1016/s1474-4422(20)30220-9

• European trends in epilepsy surgery

  Neurology · 2018 · https://doi.org/10.1212/wnl.0000000000005776

• GRIN2A -related disorders: genotype and functional consequence predict phenotype

  Brain · 2018 · https://doi.org/10.1093/brain/awy304

• Expert Opinion on the Management of Lennox–Gastaut Syndrome: Treatment Algorithms and Practical Considerations

  Frontiers in Neurology · 2017 · 10.3389/fneur.2017.00505

• Histopathological Findings in Brain Tissue Obtained during Epilepsy Surgery

  New England Journal of Medicine · 2017 · https://doi.org/10.1056/nejmoa1703784

• Vagus nerve stimulation for drug‐resistant epilepsy: A European long‐term study up to 24 months in 347 children

  Epilepsia · 2014 · https://doi.org/10.1111/epi.12762

• ILAE Official Report: A practical clinical definition of epilepsy

  Epilepsia · 2014 · https://doi.org/10.1111/epi.12550

• Distinct neurological disorders with ATP1A3 mutations

  The Lancet Neurology · 2014 · https://doi.org/10.1016/s1474-4422(14)70011-0

• GRIN2A mutations in acquired epileptic aphasia and related childhood focal epilepsies and encephalopathies with speech and language dysfunction

  Nature Genetics · 2013 · https://doi.org/10.1038/ng.2726

• De novo mutations in ATP1A3 cause alternating hemiplegia of childhood

  Nature Genetics · 2012 · https://doi.org/10.1038/ng.2358

• Epileptic encephalopathies of the Landau‐Kleffner and continuous spike and waves during slow‐wave sleep types: Genomic dissection makes the link with autism

  Epilepsia · 2012 · 10.1111/j.1528-1167.2012.03559.x

• De novo mutations in ATP1A3 cause alternating hemiplegia of childhood

  Nature Genetics · 2012 · https://doi.org/10.1038/ng.2358

• Definition of drug resistant epilepsy: Consensus proposal by the ad hoc Task Force of the ILAE Commission on Therapeutic Strategies

  Epilepsia · 2009 · https://doi.org/10.1111/j.1528-1167.2009.02397.x

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

  Journal of Medical Genetics · 2008 · https://doi.org/10.1136/jmg.2008.062323

• Key clinical features to identify girls with CDKL5 mutations

  Brain · 2008 · https://doi.org/10.1093/brain/awn197

• Lennox-Gastaut syndrome: a consensus approach on diagnosis, assessment, management, and trial methodology

  The Lancet Neurology · 2008 · https://doi.org/10.1016/s1474-4422(08)70292-8

• Treatment of pediatric epilepsy: European expert opinion, 2007

  Epileptic Disorders · 2007 · https://doi.org/10.1684/epd.2007.0144

• Nocturnal Hypermotor Seizures, Suggesting Frontal Lobe Epilepsy, Can Originate in the Insula

  Epilepsia · 2006 · https://doi.org/10.1111/j.1528-1167.2006.00510.x

• Hypothalamic Hamartoma and Seizures: A Treatable Epileptic Encephalopathy

  Epilepsia · 2003 · 10.1046/j.1528-1157.2003.59102.x

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

  Neurology · 1998 · https://doi.org/10.1212/wnl.51.5.1256

Current projects

No projects listed.