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Aladdin & Gross, “Refractory status epilepticus during pregnancy secondary to cavernous angioma”

Aouam et al., “Carbamazepine-induced DRESS and HHV6 primary infection: The importance of skin tests”

Asadi-Pooya et al., “Nutritional supplements, foods, and epilepsy: Is there a relationship?

Auer et al., “History of simple febrile seizures is associated with hippocampal abnormalities in adults”

Bidmon et al., “Glutamine synthetase becomes nitrated and its activity is reduced during repetitive seizure activity in the pentylenetetrazole model of epilepsy”

Chu et al., “Erythropoietin reduces epileptogenic processes following status epilepticus”

Derry et al., “Severe autosomal dominant nocturnal frontal lobe epilepsy associated with psychiatric disorders and intellectual disability”

Deshpande et al., “Carisbamate prevents the development and expression of spontaneous recurrent epileptiform discharges and is neuroprotective in cultured hippocampal neurons”

Gastens et al., “Predictors of pharmacoresistant epilepsy: Pharmacoresistant rats differ from pharmacoresponsive rats in behavioral and cognitive abnormalities associated with experimentally induced epilepsy”

Gong et al., “Insights into the sequence of structural consequences of convulsive status epilepticus: A longitudinal MRI study”

Grabenstatter & Dudek, “A new potential AED, carisbamate, substantially reduces spontaneous motor seizures in rats with kainate-induced epilepsy”

Jacobs et al., “Interictal high-frequency oscillations (80–500 Hz) are an indicator of seizure onset areas independent of spikes in the human epileptic brain”

Kurz et al., “A cellular mechanism for dendritic spine loss in the pilocarpine model of status epilepticus”

Lado & Moshé, “How do seizures stop?”

Mazarati et al., “Antiepileptogenic and antiictogenic effects of retigabine under conditions of rapid kindling: An ontogenic study”

Misra et al., “Impaired Nav1.2 function and reduced cell surface expression in benign familial neonatal-infantile seizures”

Mosyagin et al., “Association of ABCB1 genetic variants 3435C>T and 2677G>T to ABCB1 mRNA and protein expression in brain tissue from refractory epilepsy patients”

Reynolds & Wilson, “Psychoses of epilepsy in Babylon: The oldest account of the disorder”

Rheims et al., “Analysis of clinical patterns and underlying epileptogenic zones of hypermotor seizures”

Roulet-Perez et al., “Glut-1 deficiency syndrome masquerading as idiopathic generalized epilepsy”

Sahota et al., “Seizure type, antiepileptic drugs, and reproductive endocrine dysfunction in Indian women with epilepsy: A cross-sectional study”

Spencer et al., “Interictal spikes on intracranial recording: Behavior, physiology, and implications”

Tsiropoulos et al., “Exposure to antiepileptic drugs and the risk of hip fracture: A case-control study”

Tuan et al., “The prevalence of epilepsy in a rural district of Vietnam: A population-based study from the EPIBAVI project”

Vinogradova, “Audiogenic kindling in Wistar and WAG/Rij rats: Kindling-prone and kindling-resistant subpopulations”

Wang et al., “Microchromosomal deletions involving SCN1A and adjacent genes in severe myoclonic epilepsy in infancy”

Weber et al., “A BFIS-like syndrome with late onset and febrile seizures: Suggestive linkage to chromosome 16p11.2–16q12.1”

Winkler et al., “The head nodding syndrome: Classification and possible causes”

Zangaladze et al., “Characteristics and clinical significance of subclinical seizures”