A Slide Atlas of Epilepsy

Incidence and cumulative incidence, prevalence and mortality rates; infantile spasms and developmental delay; Lennox-Gastaut syndrome; infrequent partial seizures; generalized tonic-clonic seizure; juvenile myoclonic epilepsy; juvenile-onset typical absence epilepsy; causes of seizures and epilepsy by age; perinatal intraventricular haemorrhage; congenital toxoplasma infection; hemimegalencephaly; type I lissencephaly; schizencephaly; Aicardi syndrome; age of onset of rare neurodegenerative conditions; "ragged red" fibres; lysosomal enzyme deficiency; testosterone (T); subacute spongiform encephalopathy; Alzheimer's disease; tuberous sclerosis; Sturge-Weber syndrome; cerebral abscess; herpes simplex encephalitis; neurocysticercosis; subacute sclerosing panencephalitis; Rasmussen's "encephalitis"; idiopathic generalized epilepsy (IGE); sibling risk for epilepsy; Mendelian epilepsy gene map; risk of epilepsy associated with various cerebral insults; extradural haemotoma; acute subdural haematoma; etiology of newly diagnosed epilepsy; glioblastoma multiforme; low-grade astrocytoma; meningioma; cerebral secondaries; risks of seizure after stroke; cerebral infarction; intracerebral haemotoma; percentage of patients achieving remission; actuarial percentage of patients remaning seizure-free with continued treatment compared with slow withdrawal.