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Epilepsy

Epilepsy diagram by Designua, Shutterstock
Designua, Shutterstock

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

Top 20 most recent papers
Nature Medicine

Visualization of AMPA receptors in living human brain with positron emission tomography

Nature MedicineJanuary 22, 2020
Tomoyuki MiyazakiTakuya Takahashi
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology

A survey on clinical pathways of patients with epilepsy and cerebrovascular diseases or brain tumors

Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical NeurophysiologyJanuary 20, 2020
Gaetano ZaccaraDanilo Toni
1
Trends in Neurosciences

Ion Channel Functions in Early Brain Development

Trends in NeurosciencesJanuary 22, 2020
Richard S Smith, Christopher A Walsh
Clinical Genetics

Variants in NGLY1 lead to intellectual disability, myoclonus epilepsy, sensorimotor axonal polyneuropathy and mitochondrial dysfunction

Clinical GeneticsJanuary 21, 2020
Daan M PannemanRichard J Rodenburg
JAMA Neurology

Assessment of the Predictive Value of Outpatient Smartphone Videos for Diagnosis of Epileptic Seizures

JAMA NeurologyJanuary 22, 2020
William O TatumOSmartViE Investigators
Neuropharmacology

Modifying genetic epilepsies - Results from studies on tuberous sclerosis complex

NeuropharmacologyJanuary 22, 2020
Sergiusz JozwiakMartina Bebin
Radiology

Contralateral Preoperative Resting-State Functional MRI Network Integration Is Associated with Surgical Outcome in Temporal Lobe Epilepsy

RadiologyJanuary 22, 2020
Matthew N DeSalvoSteven M Stufflebeam
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society

Re: Time to move beyond genetics towards biomedical data-driven translational genomic research in severe paediatric epilepsies

European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology SocietyJanuary 21, 2020
Michael R Johnson
Epilepsy & Behavior : E&B

Efficacy and safety of adjunctive perampanel in adolescent patients with epilepsy: Post hoc analysis of six randomized studies

Epilepsy & Behavior : E&BJanuary 20, 2020
J Eric Piña-GarzaManoj Malhotra
2
Journal of Neural Transmission

Treatment of tics associated with Tourette syndrome

Journal of Neural TransmissionJanuary 20, 2020
Joseph Jankovic
2
Epilepsia

Genetic diagnoses in epilepsy: The impact of dynamic exome analysis in a pediatric cohort

EpilepsiaJanuary 21, 2020
Anne RochtusAnnapurna Poduri
11
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia

ATP1A3-related epilepsy: Report of seven cases and literature-based analysis of treatment response

Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of AustralasiaJanuary 22, 2020
Marius GasserCelina von Stülpnagel
Epilepsy & Behavior : E&B

Physically active children with epilepsy have good objective sleep duration and efficiency despite subjective reports of fatigue and sleep problems

Epilepsy & Behavior : E&BJanuary 21, 2020
Jeffrey DoDaniela Pohl
Seizure : the Journal of the British Epilepsy Association

Intubation for Psychogenic Non-Epileptic Attacks: Frequency, Risk Factors, and Impact on Outcome

Seizure : the Journal of the British Epilepsy AssociationJanuary 21, 2020
Tanuwong ViarasilpaStephan A Mayer
NeuroImage

Four-dimensional map of direct effective connectivity from posterior visual areas

NeuroImageJanuary 21, 2020
Ayaka SugiuraEishi Asano
Drug and Alcohol Dependence

Is time elapsed between cannabis use and sleep start time associated with sleep continuity? An experience sampling method

Drug and Alcohol DependenceJanuary 20, 2020
Sharon R SznitmanTalya Greene
8
1
Epilepsy & Behavior : E&B

The other side of the leaf: Seizures associated with synthetic cannabinoid use

Epilepsy & Behavior : E&BJanuary 21, 2020
Kuhilan GounderNicholas Lawn
3
Epilepsia

Neuropeptide depletion in the amygdala in sudden unexpected death in epilepsy: A postmortem study

EpilepsiaJanuary 21, 2020
Alyma SomaniMaria Thom
Neuroscience and Biobehavioral Reviews

The anticonvulsant effects of cannabidiol in experimental models of epileptic seizures: from behavior and mechanisms to clinical insights

Neuroscience and Biobehavioral ReviewsJanuary 20, 2020
Willian Lazarini-LopesNorberto Garcia-Cairasco
8
Epilepsy Research

Prenatal betamethasone exposure increases corticotropin-releasing hormone expression along with increased hippocampal slice excitability in the developing hippocampus

Epilepsy ResearchJanuary 20, 2020
Melissa J BensonLibor Velíšek
4

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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.

Benign Rolandic Epilepsy

Benign Rolandic epilepsy is a partial idiopathic epilepsy of childhood presenting with a nocturnal seizure and with a typical EEG showing centrotemporal spike and multifocal or generalized sharp slow waves. Here is the latest research.

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

Lafora disease is an inherited neurodegenerative disorder characterized by the presence of abnormal glycogen inclusions, called Lafora bodies, in neurons and other tissues. Here is the latest research on this fatal, autosomal recessive disorder.

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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