Results 21 to 30 of about 1,856,030 (259)
Bezmiâlem Science, 2020 Mutations in genes encoding the formation of ion channels may cause epileptic syndromes. These epileptic syndromes are generally divided into generalized and partial epilepsies.
Halil Aziz VELİOĞLU +1 more
doaj +1 more source
The Egyptian Journal of Neurology, Psychiatry and Neurosurgery, 2020 Background Epilepsy is a chronic neurological disease. A suitable biomarker for epilepsy diagnosis remains lacking. MicroRNAs (miRNAs) were pronounced as promising biomarkers for epileptogenesis. Objectives To analyze the expression levels of miR 194-5p,
Mervat Moustafa +5 more
doaj +1 more source
Neurologijos seminarai, 2019 ntroduction. The sensitivity of EEG is increased by performing standard provocative tests. The effects of additional cognitive tasks on bioelectrical brain activity aren’t widely studied.
G. Seniut +2 more
doaj +1 more source
Epilepsy is an important feature of KBG syndrome associated with poorer developmental outcome
Epilepsia Open, 2023 Objective The aim of this study was to describe the epilepsy phenotype in a large international cohort of patients with KBG syndrome and to study a possible genotype–phenotype correlation.
Nathan Buijsse +19 more
doaj +1 more source
Problems of diagnosing focal cortical dysplasia
Эпилепсия и пароксизмальные состояния, 2021 Focal cortical dysplasia (FCD) is one of the most common causes in developing pharmacoresistant epilepsy. We present the clinical case of the patient with generalized seizures.
K. D. Yakovleva +2 more
doaj +1 more source
Benign partial epilepsy with secondarily generalized seizures in infancy
Definitions, 2020 Benign partial epilepsy with secondarily generalized seizures in infancy. ORPHA:166302 Benign partial epilepsy with secondarily generalized seizures in infancy is a rare infantile epilepsy syndrome characterized by seizures presenting with motion arrest ...
semanticscholar +1 more source
Balkan Medical Journal, 2023 Background: Idiopathic generalized epilepsy is the most common group of epilepsy disorders in children and adolescents. Various types of genetic abnormality were identified among the hereditary factors that explain epilepsy.
Engin Atlı +6 more
doaj +1 more source
A variant of idiopathic epilepsy: Clinical note
Неврология, нейропсихиатрия, психосоматика, 2015 The paper describes a clinical case of idiopathic generalized epilepsy with a variable phenotype, a similar type of epileptiform activity in the second stage of sleep, and a similar genotype in siblings.
V. A. Karlov +3 more
doaj +1 more source
Migreine and periictal headache in patients with epilepsy [PDF]
Саратовский научно-медицинский журнал, 2016 Migraine and epilepsy are diseases characterized by paroxysmal occurring clinical manifestations that have different mechanisms of pathogenesis. In the interictal period in 59% of patients with epilepsy there are different types of primary headache: 18%,
Muzalevskaia D.S. +2 more
doaj
Research on the Direction of Ion Channel Related to Epileptic Seizures [PDF]
E3S Web of Conferences, 2020 Epilepsy is a group of chronic brain diseases characterized by transient central nervous system dysfunction caused by repeated abnormal synchronization of neuronal discharges in the brain, with sudden onset and repeated seizures. Epilepsy has been listed
Yin Jianing
doaj +1 more source