Epilepsy

Epilepsy is a chronic neurological disorder characterized by unprovoked and recurrent seizures. Discover the latest research on factors and mechanisms that underlie epilepsy here.

July 9, 2020

Mutations in the exocyst component EXOC2 cause severe defects in human brain development

The Journal of Experimental Medicine
Nicole J Van BergenJohn Christodoulou
July 10, 2020
Case Report

Valproic acid and zonisamide induced hyperammonemic encephalopathy

Clinical Neurology and Neurosurgery
Hristelina S IlievaJohn E Croom
July 9, 2020
Review
Open Access

Neuronal Cav3 channelopathies: recent progress and perspectives

Pflügers Archiv : European journal of physiology
Philippe LoryArnaud Monteil
July 9, 2020
Review
Open Access

Pharmacological Manipulation of K v 7 Channels as a New Therapeutic Tool for Multiple Brain Disorders

Frontiers in Physiology
Fabio A VigilMark S Shapiro
July 10, 2020
Review
Open Access

STXBP1 Encephalopathies: Clinical Spectrum, Disease Mechanisms and Therapeutic Strategies

Journal of Neurochemistry
Debra AbramovJacqueline Burré
July 10, 2020

Cost effectiveness of surgery for drug resistant temporal lobe epilepsy in the US

Neurology
Shehryar R SheikhLara Jehi
July 9, 2020

PANNEXIN 1 CHANNELS AS A THERAPEUTIC TARGET: STRUCTURE, INHIBITION, AND OUTLOOK

ACS Chemical Neuroscience
Kathleen E NavisDarren J Derksen
July 10, 2020
Case Report

Cognitive and behavioral outcome of stereotactic laser amydalohippocampotomy in a pediatric setting

Epilepsy & Behavior Reports
Kim E OnoDaniel L Drane
July 10, 2020
Comment / Editorial

Epilepsy surgery: Expensive, but worth the "price" of admission!

Neurology
John W MillerGreg D Cascino
July 10, 2020

Defining the phenotype of FHF1 developmental and epileptic encephalopathy

Epilepsia
Marina TrivisanoNicola Specchio
July 10, 2020
Review
Open Access

Bridging the healthcare gap: Building the case for epilepsy virtual clinics in the current healthcare environment

Epilepsy & Behavior : E&B
Bruce LavinMartin J Brodie
July 10, 2020

Biomarker stratigraphy in the Athel Trough of the South Oman Salt Basin at the Ediacaran-Cambrian Boundary

Geobiology
Anaïs RousselRoger E Summons
July 10, 2020

Ictal SPECT in Psychogenic Nonepileptic and Epileptic Seizures

Psychosomatics
Jose Gallucci-NetoRenato Luiz Marchetti
July 10, 2020

Expectations and knowledge of cannabidiol therapy for childhood epilepsy - A German caregiver survey

Epilepsy & Behavior : E&B
Kerstin Alexandra KlotzJulia Jacobs
July 9, 2020

EEG Findings in Coronavirus Disease

Journal of Clinical Neurophysiology : Official Publication of the American Electroencephalographic Society
Madison S PilatoJoanna S Fong-Isariyawongse
July 10, 2020

Clinical factors associated with mood affective disorders among adults with cerebral palsy

Neurology. Clinical Practice
Daniel G WhitneyMark D Peterson

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Absence Epilepsy

Absence epilepsy is a common seizure disorder in children which can produce chronic psychosocial sequelae. Discover the latest research on absence epilepsies here.

Angelman Syndrome

Angelman syndrome is a neurogenetic imprinting disorder caused by loss of the maternally inherited UBE3A gene and is characterized by generalized epilepsy, limited expressive speech, sleep dysfunction, and movement disorders. Here is the latest research.

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Dravet Syndrome

Dravet syndrome, previously known as severe myoclonic epilepsy of infancy (SMEI), is a rare, catastrophic, lifelong form of epilepsy with frequent and/or prolonged seizures that are often triggered by hot temperatures or fever. Discover the latest research on Dravet syndrome here.

Drug Resistant Epilepsy

Drug-resistant epilepsy, also known as refractory or pharmacoresistant epilepsy, is defined as failure of adequate trials of two appropriate and tolerated antiepileptic drugs (as monotherapies or in combination) to achieve sustained seizure freedom. Discover the latest research on drug-resistant epilepsy here.

Early Myoclonic Encephalopathy

Early myoclonic encephalopathy is an epileptic syndrome typically diagnosed by three months of age. It is characterized by frequent seizures and severe early encephalopathy and has a severely reduced life expectancy. Causes can include metabolic abnormalities or genetic mutations. Find the latest research on early myoclonic encephalopathy here.

Frontal Lobe Epilepsy

Frontal lobe epilepsy is characterized by brief, recurring seizures, often during sleep. Depending on the areas of the brain that are affected, these seizures may be asymptomatic or present with motor or verbal symptoms. Find the latest research on frontal lobe epilepsy here.

Juvenile Myoclonic Epilepsy

Juvenile myoclonic epilepsy, previously known as idiopathic generalized epilepsy, is a form of generalized epilepsy whose cause is presumed to be genetic in origin. The first seizure typically occurs between the ages of 5-12, and symptoms may improve after the fourth decade of life. Seizure may be of different subtypes, including absence, myoclonic, and tonic-clonic. Find the latest research on juvenile myoclinic epilepsy here.

Lafora Disease

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Landau-Kleffner Syndrome

Landau Kleffner syndrome (LKS), also called infantile acquired aphasia, acquired epileptic aphasia, or aphasia with convulsive disorder, is a rare childhood neurological syndrome characterized by the sudden or gradual development of aphasia (the inability to understand or express language) and an abnormal electroencephalogram. Discover the latest research on LKS here.

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