| Roadmap for a competency-based educational curriculum in epileptology: report of the Epilepsy Education Task Force of the International League Against Epilepsy |
18 |
| Classification of paroxysmal events and the four-dimensional epilepsy classification system |
13 |
| Epilepsy surgery for patients with genetic refractory epilepsy: a systematic review |
11 |
| Management of epilepsy in pregnancy: a report from the International League Against Epilepsy Task Force on Women and Pregnancy |
10 |
| Encephalopathy related to Status Epilepticus during slow Sleep: current concepts and future directions |
9 |
| Genetic literacy series: genetic epilepsy with febrile seizures plus |
8 |
| Loss of responsiveness in psychogenic non-epileptic seizures |
8 |
| Indications and expectations for neuropsychological assessment in epilepsy surgery in children and adults: Report of the ILAE Neuropsychology Task Force Diagnostic Methods Commission: 2017-2021 Neuropsychological assessment in epilepsy surgery |
7 |
| Current treatment options for Encephalopathy related to Status Epilepticus during slow Sleep |
6 |
| The natural history of nodding syndrome |
6 |
| The 2017 ILAE classification of seizure types and the epilepsies: what do people with epilepsy and their caregivers need to know? |
6 |
| Epilepsy for primary health care: a cost-effective Latin American E-learning initiative |
6 |
| Update on the genetics of the epilepsy-aphasia spectrum and role of GRIN2A mutations |
5 |
| EEG features in Encephalopathy related to Status Epilepticus during slow Sleep |
5 |
| Faciobrachial dystonic seizures expressed as epileptic spasms, followed by focal seizures in anti-LGI1 encephalitis: a video-polygraphic study |
5 |
| Epileptic seizure semiology in different age groups |
5 |
| Quinidine therapy and therapeutic drug monitoring in four patients with KCNT1 mutations |
5 |
| Neonatal tremor episodes and hyperekplexia-like presentation at onset in a child with SCN8A developmental and epileptic encephalopathy |
4 |
| Interictal epileptiform discharges in sleep and the role of the thalamus in Encephalopathy related to Status Epilepticus during slow Sleep |
4 |
| Encephalopathy related to Status Epilepticus during slow Sleep: a link with sleep homeostasis? |
4 |
| A novel mutation in KCNQ3-related benign familial neonatal epilepsy: electroclinical features and neurodevelopmental outcome |
4 |
| Selective deep brain stimulation in the substantia nigra reduces myoclonus in progressive myoclonic epilepsy: a novel observation and short review of the literature |
4 |
| De novo late-onset absence status epilepticus or late-onset idiopathic generalized epilepsy? A case report and systematic review of the literature |
4 |
| Lacosamide for SCN2A-related intractable neonatal and infantile seizures |
4 |
| Encephalopathy related to Status Epilepticus during slow Sleep: from concepts to terminology |
4 |
| Temporal encephalocele: a novel indication for magnetic resonance-guided laser interstitial thermal therapy for medically intractable epilepsy |
3 |
| Ictal laryngospasm monitored by video-EEG and polygraphy: a potential SUDEP mechanism |
3 |
| Investigation of paediatric occipital epilepsy using stereo-EEG reveals a better surgical outcome than in adults, especially when the supracalcarine area is affected |
3 |
| Epilepsy surgery for polymicrogyria: a challenge to be undertaken |
3 |
| Sleep-related hypermotor epilepsy and peri-ictal hypotension in a patient with syntaxin-1B mutation |
3 |
| Quantitative EEG analysis in Encephalopathy related to Status Epilepticus during slow Sleep |
3 |
| The aetiology of psychogenic non-epileptic seizures: risk factors and comorbidities |
3 |
| Rufinamide for the treatment of Lennox-Gastaut syndrome: evidence from clinical trials and clinical practice |
3 |
| Antiepileptic drugs: evolution of our knowledge and changes in drug trials |
3 |
| Cognitive impairment and behavioral disorders in Encephalopathy related to Status Epilepticus during slow Sleep: diagnostic assessment and outcome |
3 |
| Berardinelli-Seip syndrome and progressive myoclonus epilepsy |
3 |
| Biallelic loss-of-function UBA5 mutations in a patient with intractable West syndrome and profound failure to thrive |
3 |
| Identifying the educational needs of physicians in pediatric epilepsy in order to improve care: results from a needs assessment in Germany, Spain, and the United States |
3 |
| Inadequate benzodiazepine dosing may result in progression to refractory and non-convulsive status epilepticus |
2 |
| Under-reporting of sudden unexpected death in epilepsy |
2 |
| A triad of infantile spasms, nystagmus and a focal tonic seizure |
2 |
| A child with hyperekplexia and epileptic myoclonus |
2 |
| Probable dysimmune epilepsia partialis continua manifesting as epileptic moving toes syndrome: electroclinical features of a challenging case |
2 |
| A comprehensive clinico-pathological and genetic evaluation of bottom-of-sulcus focal cortical dysplasia in patients with difficult-to-localize focal epilepsy |
2 |
| Progressive intellectual impairment in children with Encephalopathy related to Status Epilepticus during slow Sleep |
2 |
| Early and long-term electroclinical features of patients with epilepsy and PCDH19 mutation |
2 |
| KCNQ2 mutation in an infant with encephalopathy of infancy with migrating focal seizures |
2 |
| Cortical surface intracranial electrodes identify clinically relevant seizures missed on scalp EEG after traumatic intracranial hemorrhage |
2 |
| Brainstem lesion causing paroxysmal ataxia, dysarthria, diplopia and hemifacial spasm (PADDHS) |
2 |
| Atypical postictal transient subcortical T2 hypointensity in a newly diagnosed diabetic patient with seizures |
2 |
