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Attention profiles in childhood absence epilepsy compared with attention-deficit/hyperactivity disorder.
Fast oscillation dynamics during hypsarrhythmia as a localization biomarker.
A New Rat Model of Epileptic Spasms Based on Methylazoxymethanol-Induced Malformations of Cortical Development.
Chronic Eosinophilic Meningoencephalitis by Prototheca Wickerhamii in an Immunocompetent Boy.
Clinical Characteristics of Transplant-associated Encephalopathy in Children.
Large-scale structural alteration of brain in epileptic children with SCN1A mutation.
Short-Term Outcome of Intravenous Methylprednisolone Pulse Therapy in Patients With Infantile Spasms.
An interictal EEG can predict the outcome of vagus nerve stimulation therapy for children with intractable epilepsy.
Children Experiencing First-Time or Prolonged Febrile Seizure Are Prone to Stress Hyperglycemia.
Epilepsy and Other Neuropsychiatric Manifestations in Children and Adolescents with 22q11.2 Deletion Syndrome.
Genotype-Phenotype Correlation of SMN1 and NAIP Deletions in Korean Patients with Spinal Muscular Atrophy.
Intravenous levetiracetam versus phenobarbital in children with status epilepticus or acute repetitive seizures.
Obsessive-Compulsive Disorder Related to Mycoplasma-Associated Autoimmune Encephalopathy with Basal Ganglia Involvement.
Two cases of familial cerebral cavernous malformation caused by mutations in the CCM1 gene..
A Rare Case of Childhood Stiff Person Syndrome Associated With Pleuropulmonary Blastoma.
Cognitive function in childhood epilepsy: importance of attention deficit hyperactivity disorder.
Importance of RNF213 polymorphism on clinical features and long-term outcome in moyamoya disease.
Structural abnormalities in benign childhood epilepsy with centrotemporal spikes (BCECTS).
β-Hydroxybutyrate attenuates NMDA-induced spasms in rats with evidence of neuronal stabilization on MR spectroscopy.
A potential effect of ganaxolone in an animal model of infantile spasms.
Attention-deficit/hyperactivity disorder and attention impairment in children with benign childhood epilepsy with centrotemporal spikes.
Epilepsy phenotype associated with a chromosome 2q24.3 deletion involving SCN1A: Migrating partial seizures of infancy or atypical Dravet syndrome?
Long-term outcomes of hemispheric disconnection in pediatric patients with intractable epilepsy.
Risk factors for neurological complications and their correlation with survival following pediatric liver transplantation.
Central nervous system involvement is a critical prognostic factor for hemophagocytic lymphohistiocytosis
β-Hydroxybutyrate increases the pilocarpine-induced seizure threshold in young mice.
Neuropsychological status of children with newly diagnosed idiopathic childhood epilepsy.
Risk Factors and Clinical Outcomes of Childhood Ischemic Stroke in a Single Korean Tertiary Care Center.
Surgical treatment for localization-related infantile spasms: Excellent long-term outcomes.
Electroencephalographic generalized features in idiopathic childhood focal epilepsies.