Results 261 to 270 of about 2,272,583 (371)

Adult phenotypes of genetic developmental and epileptic encephalopathies. [PDF]

open access: yesBrain Commun
Vakrinou A   +5 more
europepmc   +1 more source

Clinical and anatomical characteristics of basal temporal seizures: A systematic review

open access: yesEpileptic Disorders, EarlyView.
Abstract This review aimed to characterize the clinical semiology and anatomical correlates of seizures originating in the basal temporal region, an underrecognized epilepsy subtype, and to identify features that distinguish it from other forms of temporal lobe epilepsies (TLE).
Fabrice Bartolomei   +2 more
wiley   +1 more source

Exploring biomarkers of neurodegeneration in epilepsy: Critical insights

open access: yesEpileptic Disorders, EarlyView.
Abstract The advent of biofluid biomarkers for neurodegenerative disorders has precipitated a surge in recent evidence regarding their role in epilepsy. In this literature review, we examine the diagnostic, prognostic, and therapeutic potential of several biomarkers, including amyloid‐beta (Aβ) protein, total (t‐tau), phosphorylated tau (p‐tau) protein,
Rida Farhan   +7 more
wiley   +1 more source

Pulmonary vascular malformations in genetic epileptic encephalopathy: A rare, fatal case report. [PDF]

open access: yesRespir Med Case Rep
Garancini N   +7 more
europepmc   +1 more source

Adult‐onset epilepsy with startle‐induced seizure after febrile infection‐related epilepsy syndrome: A case report

open access: yesEpileptic Disorders, EarlyView.
Abstract Startle‐induced seizure is a rare type of reflex seizure triggered by unexpected sensory stimuli that often occurs in children with early acquired cerebral lesions or brain malformations. We report a unique case of adult‐onset epilepsy with startle‐induced seizures.
Kazutoshi Konomatsu   +12 more
wiley   +1 more source

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