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The maestro don Gonzalo Rodriguez-Lafora
Seizures in multiple sclerosis
Injuries in people with self-reported epilepsy: A population-based study
The diagnostic value of oral lacerations and incontinence during convulsive seizures
Focal motor seizures induced by alerting stimuli in critically ill patients
Incidence of seizures in the acute phase of stroke: A population-based study
Autonomic consequences of kainic acidinduced limbic cortical seizures in rats: Peripheral autonomic nerve activity, acute cardiovascular changes, and death
Prenatal freeze lesioning produces epileptogenic focal cortical dysplasia
Interictal regional polyspikes in noninvasive EEG suggest cortical dysplasia as etiology of focal epilepsies
Cortical auditory dysfunction in benign rolandic epilepsy
The three stages of epilepsy in patients with CDKL5 mutations
Homozygous W748S mutation in the POLG1 gene in patients with juvenile-onset Alpers syndrome and status epilepticus
Mesial temporal lobe epilepsy: Clinical and neuropathologic findings of familial and sporadic forms
Possible role of the innate immunity in temporal lobe epilepsy
Seizures following picornavirus infection
Plasma concentrations of lamotrigine and its 2-N-glucuronide metabolite during pregnancy in women with epilepsy
Circalunar and ultralunar periodicities in women with partial seizures
An autosomal dominant genetically heterogeneous variant of rolandic epilepsy and speech disorder
Balanced translocation in a patient with severe myoclonic epilepsy of infancy disrupts the sodium channel gene SCN1A
Wind turbines, flicker, and photosensitive epilepsy: Characterizing the flashing that may precipitate seizures and optimizing guidelines to prevent them
Headache in patients with epilepsy: A prospective incidence study
Three new forms of familial epilepsy syndromes in the proposed diagnostic scheme of the ILAE (2001): A clinical experience in Southwest China
Seven novel SCN1A mutations in Chinese patients with severe myoclonic epilepsy of infancy
Do SCN1A mutations protect from hippocampal sclerosis
A functional polymorphism in the SCN1A gene is not associated with carbamazepine dosages in Austrian patients with epilepsy
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