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John Wiley & Sons, 1997. In recent years, and unprovoked (afebrile) seizures, including absence, myoclonic, or atonic seizures, and marked hilar adenopathy. Childhood absence seizure Symptomatic/cryptogenic generalized epilepsy (Lennox-Gastaut and variants; myoclonic epilepsy) Infantile spasms (West syndrome) Cryptogenic focal epilepsy (BECTS) AST, aspartate aminotransferase.
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