All Stories

  1. Deciphering the Natural History of SCN8A -Related Disorders
  2. Variants in ATP6V0C are associated with Dravet‐like developmental and epileptic encephalopathy
  3. The epilepsy–autism phenotype associated with developmental and epileptic encephalopathies: New mechanism‐based therapeutic options
  4. Global modified Delphi consensus on diagnosis, phenotypes, and treatment of SCN8A‐related epilepsy and/or neurodevelopmental disorders
  5. Gain-of-function and loss-of-function GABRB3 variants lead to distinct clinical phenotypes in patients with developmental and epileptic encephalopathies
  6. KCNT1-related epilepsies and epileptic encephalopathies: phenotypic and mutational spectrum
  7. Recent advances in treatment of epilepsy-related sodium channelopathies
  8. The spectrum of intermediate SCN8A‐related epilepsy
  9. Neurologic phenotypes associated with COL4A1 / 2 mutations
  10. Correction: IQSEC2-related encephalopathy in males and females: a comparative study including 37 novel patients
  11. The phenotype of SCN8A developmental and epileptic encephalopathy
  12. IQSEC2-related encephalopathy in males and females: a comparative study including 37 novel patients
  13. Early mortality in SCN8A -related epilepsies
  14. Standardisierter Computer-basiert-organisierter Report des EEG (SCORE) – Eine strukturierende Form der EEG-Befundung
  15. The epilepsy phenotypic spectrum associated with a recurrent CUX2 variant
  16. Diagnostic yield of standard-wake and sleep EEG recordings
  17. Defining the phenotypic spectrum of SLC6A1 mutations
  18. Added clinical value of the inferior temporal EEG electrode chain
  19. Standardized computer-based organized reporting of EEG: SCORE – Second version
  20. Remission of encephalopathy with status epilepticus (ESES) during sleep renormalizes regulation of slow wave sleep
  21. Clinical spectrum and genotype–phenotype associations of KCNA2-related encephalopathies
  22. Do patients need to stay in bed all day in the Epilepsy Monitoring Unit? Safety data from a non-restrictive setting
  23. Alternating hemiplegia of childhood and a pathogenic variant of ATP1A3: a case report and pathophysiological considerations
  24. Myoclonus epilepsy and ataxia due toKCNC1mutation: Analysis of 20 cases and K+channel properties
  25. Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders
  26. Salzburg criteria: can we extend validation to critical care? – Authors' reply
  27. Phenotypic spectrum of GABRA1
  28. Diagnostic accuracy of the Salzburg EEG criteria for non-convulsive status epilepticus: a retrospective study
  29. Reply
  30. Benign infantile seizures and paroxysmal dyskinesia caused by anSCN8Amutation
  31. Diagnostic yield of five minutes compared to three minutes hyperventilation during electroencephalography
  32. Salzburg Consensus Criteria for Non-Convulsive Status Epilepticus – approach to clinical application
  33. Mutations inKCNT1cause a spectrum of focal epilepsies
  34. The phenotypic spectrum of SCN8A encephalopathy
  35. Encephalopathy with status epilepticus during sleep (ESES) induced by oxcarbazepine in idiopathic focal epilepsy in childhood
  36. How long shall we record electroencephalography?
  37. Endoscopic laryngeal patterns in vagus nerve stimulation therapy for drug-resistant epilepsy
  38. Focal epilepsies in adult patients attending two epilepsy centers: Classification of drug-resistance, assessment of risk factors, and usefulness of “new” antiepileptic drugs
  39. Patients with epilepsy and patients with psychogenic non-epileptic seizures: Video-EEG, clinical and neuropsychological evaluation
  40. Epilepsy in adult patients with Down syndrome: a clinical‐video EEG study
  41. Neuroethological approach to frontolimbic epileptic seizures and parasomnias: The same central pattern generators for the same behaviours
  42. Idiopathic generalized epilepsy (IGE) syndromes in development: IGE with absences of early childhood, IGE with phantom absences, and perioral myoclonia with absences
  43. Seizure‐related automatic locomotion triggered by intracerebral electrical stimulation
  44. Possible post‐traumatic paroxysmal kinesigenic dyskinesia
  45. Age‐Related Gender Differences in Reporting Ictal Fear: Analysis of Case Histories and Review of the Literature
  46. Ictal Grasping: Prevalence and Characteristics in Seizures with Different Semiology
  47. Autosomal Dominant Early‐onset Cortical Myoclonus, Photic‐induced Myoclonus, and Epilepsy in a Large Pedigree
  48. Lesionectomy in epileptogenic gangliogliomas: Seizure outcome and surgical results
  49. Central pattern generators for a common semiology in fronto-limbic seizures and in parasomnias. A neuroethologic approach
  50. Telephone‐induced Seizures: A New Type of Reflex Epilepsy
  51. Facial Expression of Emotion in Human Frontal and Temporal Lobe Epileptic Seizures
  52. Epileptic intermittent snoring
  53. A video-polygraphic analysis of the cataplectic attack
  54. Encephalopathy with electrical status epilepticus during slow sleep or ESES syndrome including the acquired aphasia
  55. Photic Reflex Myoclonus: A Neurophysiological Study in Progressive Myoclonus Epilepsies
  56. Electroclinical features of idiopathic generalised epilepsy with persisting absences in adult life.
  57. Transcranial magnetic stimulation in partial epilepsy: drug-induced changes of motor excitability
  58. A wavelet based analysis of energy redistribution in scalp EEG during epileptic seizures