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Articles: Seizure |
Prior Articles
Emotional recognition in depressed epilepsy patients
Epilepsy and Behavior, 07/29/09
Can hypnosis differentiate epileptic from nonepileptic events in the video/EEG monitoring unit? Data from a pilot study
Epilepsy and Behavior, 07/29/09 A description of current practice in epilepsy monitoring units
Epilepsy and Behavior, 07/29/09 Dynamic statistical parametric mapping for analyzing ictal magnetoencephalographic spikes in patients with intractable frontal lobe epilepsy
Epilepsy Research, 07/29/09 High frequency oscillations and seizure frequency in patients with focal epilepsy
Epilepsy Research, 07/29/09 The impact of seizure-related items and comorbid medical conditions on the MMPI-2 profiles of patients with epilepsy and psychogenic nonepileptic seizures
Epilepsy and Behavior, 07/29/09 The electrophysiological "delayed effect" of focal interictal epileptiform discharges. A low resolution electromagnetic tomography (LORETA) study
Epilepsy Research, 07/29/09 Digenic mutations in severe myoclonic epilepsy of infancy
Epilepsy Research, 07/29/09 Extensive apoptosis in a case of intractable infantile status epilepticus
Epilepsy Research, 07/29/09 Efficacy and safety of levetiracetam in the treatment of Panayiotopoulos syndrome
Epilepsy Research, 07/28/09 Cardiovascular autonomic functions in well-controlled and intractable partial epilepsies
Epilepsy Research, 07/28/09 Adenosine augmentation therapies (AATs) for epilepsy: Prospect of cell and gene therapies
Epilepsy Research, 07/28/09 Giant Intradural Mucocele in a Patient with Adult Onset Seizures
Case Reports in Neurology, 07/28/09 FLIP&FLAP—A training programme for children and adolescents with epilepsy, and their parents
Seizure - European Journal of Epilepsy, 07/24/09 MEF2C haploinsufficiency caused either by microdeletion of the 5q14.3 region or mutation is responsible for severe mental retardation with stereotypic movements, epilepsy and/or cerebral malformations
Journal of Medical Genetics, 07/24/09 Physico-chemical property changes of amino acid residue accompanied with missense mutations in SCN1A affect the epilepsy phenotype severity
Journal of Medical Genetics, 07/24/09 De novo SCN1A mutations in Dravet syndrome and related epileptic encephalopathies are largely of paternal origin
Journal of Medical Genetics, 07/24/09 The metabolic syndrome in overweight epileptic patients treated with valproic acid
Epilepsia, 07/23/09 Optogenetic control of epileptiform activity
Proceedings of the National Academy of Sciences of the United States of America, 07/23/09 Vagus nerve stimulation induces changes in respiratory sinus arrhythmia of epileptic children during sleep
Epilepsia, 07/23/09
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Indexed Journals: Current Opinion in Neurology, Stroke, Seizure, Cephalgia, Brain Injury
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250 Available Pages
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