Feed Preview

Absence Epilepsy

Absence Epilepsy diagram by Der Lange, Wikimedia
Der Lange, Wikimedia

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

Top 20 most recent papers
Neuroscience

Angelman syndrome: from mouse models to therapy

NeuroscienceFebruary 24, 2020
Diana C RotaruYpe Elgersma
3
Epilepsy & Behavior : E&B

Subcortical gray matter changes in pediatric patients with new-onset juvenile myoclonic epilepsy

Epilepsy & Behavior : E&BJanuary 15, 2020
Zeynep ÖztürkZeynep Selen Karalok
1
Iranian Journal of Child Neurology

Utility of Seizure Pattern and Related Clinical Features in the Diagnosis of Neurometabolic Disorders

Iranian Journal of Child NeurologyFebruary 6, 2020
Narjes JafariShahrzad Tabatabaee
Acta Neurologica Scandinavica

Tonic-clonic seizures in idiopathic generalized epilepsies: prevalence, risk factors, and outcome

Acta Neurologica ScandinavicaFebruary 8, 2020
Ali A Asadi-Pooya, Maryam Homayoun
2
Journal of Visualized Experiments : JoVE

Inducing Post-Traumatic Epilepsy in a Mouse Model of Repetitive Diffuse Traumatic Brain Injury

Journal of Visualized Experiments : JoVEFebruary 25, 2020
Oleksii Shandra, Stefanie Robel
IEEE Transactions on Neural Systems and Rehabilitation Engineering : a Publication of the IEEE Engineering in Medicine and Biology Society

Closed-loop control of absence seizures inspired by feedback modulation of basal ganglia to the corticothalamic circuit

IEEE Transactions on Neural Systems and Rehabilitation Engineering : a Publication of the IEEE Engineering in Medicine and Biology SocietyFebruary 5, 2020
Denggui Fan, Qingyun Wang
Pharmacology

Effect of U-92032, T-Type Ca2+ Channel Blocker, on Rats with Genetic Absence Epilepsy

PharmacologyFebruary 27, 2020
Hasan Raci YananliFiliz Yılmaz Onat
Saudi Journal of Medicine & Medical Sciences

A Case Report of Intraparenchymal Neurocysticercosis in a Postpartum Female in Saudi Arabia

Saudi Journal of Medicine & Medical SciencesJanuary 14, 2020
Foziah Jabbar AlshamraniAlaa Nabil Turkistani
Epilepsia

SCN1A-related phenotypes: Epilepsy and beyond

EpilepsiaJanuary 7, 2020
Ingrid E Scheffer, Rima Nabbout
7
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA

No longer a historical ailment: two cases of childhood scurvy with recommendations for bone health providers

Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USAJanuary 7, 2020
E D AltenD R Weber
4
1
Zhonghua er ke za zhi. Chinese journal of pediatrics

Genotype and phenotype of children with KCNA2 gene related developmental and epileptic encephalopathy

Zhonghua er ke za zhi. Chinese journal of pediatricsJanuary 7, 2020
P GongZ X Yang

See more papers from this feed

Related Feeds

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.

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.

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.

© 2020 Meta ULC. All rights reserved
/feed-previews/absence-epilepsy/017a00d5-8df8-46e7-ae55-ad934e560119