Results 31 to 40 of about 38,167 (281)

Genome wide high density SNP-based linkage analysis of childhood absence epilepsy identifies a susceptibility locus on chromosome 3p23-p14

open access: yes, 2009
Childhood absence epilepsy (CAE) is an idiopathic generalised epilepsy (IGE) characterised by typical absence seizures manifested by transitory loss of awareness with 2.5–4 Hz spike-wave complexes on ictal EEG.
Sander, Thomas   +51 more
core   +1 more source

Clinical and neuropsychological assessment of attention and ADHD comorbidity in a sample of children and adolescents with idiopathic epilepsy

open access: yesArquivos de Neuro-Psiquiatria, 2015
Children with epilepsy present significant problems concerning attention and comorbidity with attention deficit hyperactivity disorder (ADHD). Objective To determine the prevalence of attention complaints, ADHD diagnosis and attention profile in a sample
Celia Regina Carvalho Machado da Costa   +3 more
doaj   +1 more source

Suicidal behavior and antiepileptic drugs in epilepsy: analysis of the emerging evidence

open access: yes, 2011
Marco Mula1, Dale C Hesdorffer21Department of Clinical and Experimental Medicine, Amedeo Avogadro University and Division of Neurology, University Hospital Maggiore della Carità, Novara, Italy; 2Gertrude H Sergievsky Center and Department of ...
Mula M   +3 more
core   +2 more sources

TREATMENT OF IDIOPATHIC EPILEPSY [PDF]

open access: yesThe Journal of Nervous and Mental Disease, 1905
n ...
openaire   +1 more source

Global, regional, and national burden of epilepsy, 1990–2021: a systematic analysis for the Global Burden of Disease Study in 2021

open access: yesCost Effectiveness and Resource Allocation
Background Idiopathic epilepsy is a serious neurological disorder that can lead to premature death and severe disability. We aimed to assess the global burden of idiopathic epilepsy, to provide a comprehensive understanding of the current dynamics and ...
Tianqi Sun, Tianfu Yu, Pengcheng Liu
doaj   +1 more source

Migreine and periictal headache in patients with epilepsy [PDF]

open access: yesСаратовский 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  

(NEW) Electrocardiographic Changes In Children With Idiopathic Epilepsy And Epilepsy Secondary To Structural Brain Lesions [PDF]

open access: yesMinia Journal of Medical Research
Background:  Several changes in autonomic functions were associated with epileptic seizures, which may contribute immediately or soon after the ictal event to cardiovascular, pulmonary, gastrointestinal, and urinary manifestations.
Marwa Ali   +3 more
doaj   +1 more source

Urinary Neurotransmitter Patterns Are Altered in Canine Epilepsy

open access: yesFrontiers in Veterinary Science, 2022
Epilepsy is the most common chronic neurological disease in humans and dogs. Epilepsy is thought to be caused by an imbalance of excitatory and inhibitory neurotransmission.
Teresa Schmidt   +9 more
doaj   +1 more source

White Matter Microstructural Abnormalities in Neonatal Onset Genetic Epilepsy

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Recent evidence indicates that epilepsy is associated with abnormal white matter. If seizures alter white matter, then the impact upon network function, epileptogenesis, and cognition could be pronounced in neonates undergoing rapid developmental myelination. Neonates with epilepsy due to nonstructural genetic causes provide a unique
Amanda G. Sandoval Karamian   +8 more
wiley   +1 more source

EEG–fMRI of idiopathic and secondarily generalized epilepsies

open access: yes, 2006
We used simultaneous EEG and functional MRI (EEG–fMRI) to study generalized spike wave activity (GSW) in idiopathic and secondary generalized epilepsy (SGE).
Lemieux, L.   +15 more
core   +1 more source

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