February 2019

Classification of paroxysmal events and the four-dimensional epilepsy classification system

EEG of asymptomatic first-degree relatives of patients with juvenile myoclonic, childhood absence and rolandic epilepsy: a systematic review and meta-analysis

DEPDC5 mutation and familial focal epilepsy with variable foci: genotype and phenotype of a family

Quinidine therapy and therapeutic drug monitoring in four patients with KCNT1 mutations

Functional brain connectivity in electrical status epilepticus in sleep

A comprehensive clinico-pathological and genetic evaluation of bottom-of-sulcus focal cortical dysplasia in patients with difficult-to-localize focal epilepsy

Neuropsychological correlates of obstructive sleep apnea severity in patients with epilepsy

A novel mutation in KCNQ3-related benign familial neonatal epilepsy: electroclinical features and neurodevelopmental outcome

Tonic status epilepticus in a centenarian woman

Absence status induced by lacosamide adjunctive therapy

Focal visual status epilepticus

Rasmussen syndrome: absence seizures may be induced by oxcarbazepine

A Rasmussen encephalitis, autoimmune encephalitis, and mitochondrial disease mimicker: expanding the DNM1L-associated intractable epilepsy and encephalopathy phenotype

Berardinelli-Seip syndrome and progressive myoclonus epilepsy

Epilepsy surgery in the first months of life: a large type IIb focal cortical dysplasia causing neonatal drug-resistant epilepsy