Book section · January 1, 2025
Theneonatal-onset electroclinical syndromes can be categorized as selflimiteddisorders or Early Infantile Developmental and Epileptic Encephalopathies(EIDEE). Self-limited syndromes include Self-Limited Neonatal Epilepsy (SeLNE)and Self-Limited Familial Ne ...
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Book section · October 11, 2019
Autosomal dominant epilepsy with auditory features (ADEAF), also referred to as autosomal dominant lateral temporal epilepsy (ADLTE), is one type of familial temporal lobe epilepsy. ...
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Book section · January 1, 2009
Many studies have demonstrated the occurrence of neuronal cell death through necrosis, apoptosis, or other forms of programmed cell death (PCD) in a number of models of status epilepticus (SE). Significant age-related, model-dependent, and regional differe ...
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Book section · January 1, 2009
Landau–Kleffner syndrome (LKS) is an acquired epileptic aphasia in which children 3–8years old, who already have developed normal speech, experience language regression with verbal auditory agnosia, abnormal epileptiform activity, and behavioral disturbanc ...
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