Results 61 to 70 of about 2,366 (197)
Genetic epilepsies with myoclonic seizures: Mechanisms and syndromes
Epilepsia Open, EarlyView.Abstract Genetic epilepsy with myoclonic seizures encompasses a heterogeneous spectrum of conditions, ranging from benign and self‐limiting forms to severe, progressive disorders. While their causes are diverse, a significant proportion stems from genetic abnormalities.
Antonietta Coppola +3 more
wiley +1 more source
STATUS EPILEPTICUS IN A PATIENT WITH RASMUSSEN’S ENCEPHALITIS
Alʹmanah Kliničeskoj Mediciny, 2016 We describe clinical case of Rasmussen's encephalitis in a 24-year-old woman that occurred during her hospital stay. Its clinical manifestations included a clonic movement disorder and partial epilepsy.
A. S. Kotov A.S. +6 more
doaj +1 more source
Rituximab in Rasmussen’s encephalitis: A single center experience and review of the literature
Epilepsy & Behavior Reports, 2022 Rasmussen's encephalitis (RE) is a rare chronic inflammatory disease of the brain resulting in unilateral hemispheric atrophy with drug-resistant focal epilepsy associated with a variable degree of progressive hemiparesis and cognitive decline.
Sujit A. Jagtap +5 more
doaj +1 more source
Ovarioleukodystrophy due to EIF2B5 mutations [PDF]
, 2016 Ovarioleukodystrophy – the co-occurrence of leukodystrophy and premature ovarian failure – is a rare presentation which is now recognised to be part of the clinical spectrum of vanishing white matter disease.
Faulkner, Howard +4 more
core +2 more sources
The epileptologist's perspective of focal cortical dysplasia type 3: From concept to management
Epilepsia, Volume 67, Issue 3, Page 1017-1031, March 2026.Abstract The recent International League Against Epilepsy (ILAE) official and updated classification of focal cortical dysplasia (FCD) includes a third type—FCD type 3—characterized by architectural abnormalities (cortical dyslamination) associated with another “principal” lesion: hippocampal sclerosis (HS), developmental tumors, vascular malformations,
André Palmini +10 more
wiley +1 more source
False localization of ictal activity by scalp EEG in candidates for hemispherectomy [PDF]
, 1993 Two patients with intractable seizures and large structural lesions were candidates for hemispherectomy for seizure control. Repeated ictal EEGs recorded from scalp falsely localized seizure onset to the contralateral hemisphere. Intracarotid amobarbital
Baram, TZ, Mitchell, WG, Snead, OC
core +1 more source
Diagnosis and treatment of occipital brain lesions in children
Developmental Medicine &Child Neurology, Volume 67, Issue 11, Page 1409-1420, November 2025.Occipital brain lesions in children represent a diagnostic challenge due to the large spectrum of etiologies and overlapping clinical features. This review analyses common and less common causes of occipital brain lesions in children, including malformative, vascular, genetic/metabolic, infectious, inflammatory, and neoplastic conditions.
Luca Bartolini +4 more
wiley +1 more source
, 1977 Seizures are a symptom and not a disease. A seizure is the result of an abnormal electrical discharge of a collection or group of living but damaged or abnormal neurons.
Suter, Cary
core +1 more source
Epileptic Disorders, Volume 27, Issue 5, Page 745-802, October 2025.Abstract Although inborn errors of metabolism (IEM) are a rare cause of epilepsy, seizures are a common presentation in these disorders. Seizures in IEM are frequently refractory to conventional anti‐seizure medication and might warrant initiation of specific treatments based on vitamins or dietary modifications or provision of alternative substrates ...
D. Kapoor +7 more
wiley +1 more source
New-Onset Refractory Status Epilepticus with Claustrum Damage: Definition of the Clinical and Neuroimaging Features [PDF]
, 2017 New-onset refractory status epilepticus (NORSE) is a rare but challenging condition occurring in a previously healthy patient, often with no identifiable cause.
Alexopoulos, Haris +11 more
core +1 more source