Abstract Listings

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OXCARBAZEPINE ADDED TO OTHER SODIUM CHANNEL BLOCKERS OR ANTIEPILEPTIC DRUGS IMPROVES SEIZURE CONTROL IN CHILDREN WITH REFRACTORY SEIZURES

Feb 5, 2021, 20:39 PM
Local resting connectivity is decreased in regions of metabolic dysfunction

Feb 5, 2021, 20:39 PM
Role of persistent sodium dependent intrinsic bursting neurons in human neocortical rhythmicity

Feb 5, 2021, 20:39 PM
The utility of behavioral intervention for improving antiepileptic drug adherence among pediatric epilepsy patients

Feb 5, 2021, 20:39 PM
What about Us? Siblings of Children with Epilepsy

Feb 5, 2021, 20:39 PM
COLLATERAL SULCUS VOLUME CHANGES IN TEMPORAL LOBE EPILEPSY

Feb 5, 2021, 20:39 PM
LANDAU-KLEFFNER SYNDROME AND MALIGNANT ROLANDIC EPILEPSY: ARE THEY THE SAME OR DIFFERENT?

Feb 5, 2021, 20:39 PM
The Phenotypic Spectrum of NEXMIF Encephalopathy

Feb 5, 2021, 20:39 PM
Benzodiazepine Prescription Profiles for New Adult Patients Referred Into the Wake Forest Comprehensive Epilepsy Center Clinic

Feb 5, 2021, 20:39 PM
Indeterminate EMU Admissions: Does Repeating the Admission Help?

Feb 5, 2021, 20:39 PM
Use of EpiNavTM software for quantitative assessment of vascular images for safe SEEG implantation planning

Feb 5, 2021, 20:39 PM
THE COMBINED DEXAMETHASONE/CRH TEST AS A BIOLOGICAL MARKER FOR THE DISCRIMINATION OF PATIENTS WITH EPILEPSY AND PSYCHOGENIC SEIZURE DISORDERS

Feb 5, 2021, 20:39 PM
An Application of Cognitive Behaviour Therapy to Non-Epileptic Seizures

Feb 5, 2021, 20:39 PM
LOSS OF SEIZURE CONTROL PRECEDES VNS BATTERY END OF SERVICE

Feb 5, 2021, 20:39 PM
The Efficacy of the Ketogenic Diet in Correlation with Beta-hydroxybuterate Level

Feb 5, 2021, 20:39 PM
TREATMENT OF COMPLEX PARTIAL EPILEPSY WITH PREGABALIN: COGNITIVE SIDE EFFECTS?

Feb 5, 2021, 20:39 PM
SEIZURE SUSCEPTIBILITY OF NEUROPEPTIDE-Y (NPY) KNOCK-OUT MICE IN ELECTRICAL KINDLING AND CHEMICALLY-INDUCED SEIZURE MODELS

Feb 5, 2021, 20:39 PM
Elvis and Epilepsy; a case of musicogenic epilepsy treated with music.

Feb 5, 2021, 20:39 PM
Further evidence of Genetic heterogeneity in families with Generalized Epilepsy with febrile seizure plus.

Feb 5, 2021, 20:39 PM
Novel SCN1A phenotype with hotspot mutation: Early Profound Developmental Epileptic Encephalopathy with Movement Disorder

Feb 5, 2021, 20:39 PM

Abstracts

OXCARBAZEPINE ADDED TO OTHER SODIUM CHANNEL BLOCKERS OR ANTIEPILEPTIC DRUGS IMPROVES SEIZURE CONTROL IN CHILDREN WITH REFRACTORY SEIZURES

Local resting connectivity is decreased in regions of metabolic dysfunction

Role of persistent sodium dependent intrinsic bursting neurons in human neocortical rhythmicity

The utility of behavioral intervention for improving antiepileptic drug adherence among pediatric epilepsy patients

What about Us? Siblings of Children with Epilepsy

COLLATERAL SULCUS VOLUME CHANGES IN TEMPORAL LOBE EPILEPSY

LANDAU-KLEFFNER SYNDROME AND MALIGNANT ROLANDIC EPILEPSY: ARE THEY THE SAME OR DIFFERENT?

The Phenotypic Spectrum of NEXMIF Encephalopathy

Benzodiazepine Prescription Profiles for New Adult Patients Referred Into the Wake Forest Comprehensive Epilepsy Center Clinic

Indeterminate EMU Admissions: Does Repeating the Admission Help?

Use of EpiNavTM software for quantitative assessment of vascular images for safe SEEG implantation planning

THE COMBINED DEXAMETHASONE/CRH TEST AS A BIOLOGICAL MARKER FOR THE DISCRIMINATION OF PATIENTS WITH EPILEPSY AND PSYCHOGENIC SEIZURE DISORDERS

An Application of Cognitive Behaviour Therapy to Non-Epileptic Seizures

LOSS OF SEIZURE CONTROL PRECEDES VNS BATTERY END OF SERVICE

The Efficacy of the Ketogenic Diet in Correlation with Beta-hydroxybuterate Level

TREATMENT OF COMPLEX PARTIAL EPILEPSY WITH PREGABALIN: COGNITIVE SIDE EFFECTS?

SEIZURE SUSCEPTIBILITY OF NEUROPEPTIDE-Y (NPY) KNOCK-OUT MICE IN ELECTRICAL KINDLING AND CHEMICALLY-INDUCED SEIZURE MODELS

Elvis and Epilepsy; a case of musicogenic epilepsy treated with music.

Further evidence of Genetic heterogeneity in families with Generalized Epilepsy with febrile seizure plus.

Novel SCN1A phenotype with hotspot mutation: Early Profound Developmental Epileptic Encephalopathy with Movement Disorder

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