EPILEPSIA MIOCLONICA JUVENIL DE JANZ PDF

Familial Juvenile Myoclonic Epilepsy. En: Advances of Neurology Proposal for revised classification of epilepsies and epileptic syndromes. Epilepsia ;

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Epilepsia ;44 2 EEG features in idiopathic generalized epilepsy. Clues to diagnosis. Epilepsia ;47 3 Focal semiologic and electroencephalographic features in patients with juvenile myoclonic epilepsy. Epilepsia ;46 10 Clinical and EEG asymmetries in juvenile myoclonic epilepsy. Epilepsia ;35 2 Meencke HJ.

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Epilepsia ;44 8 : Structural brain lesions do not influence the prognosis of juvenile myoclonic epilepsy. Acta Neurol Scand ; Gelisse, P. Genton, P. Thomas, M Rey, JC. Samuelian, C. Clinical factors of drug resistance in juvenile myoclonic epilepsy. Is the underlying cause of epilepsy a major prognostic factor for recurrence?

EEG discharges on awakening: A marker of idiopathic generalized epilepsy. The relationship between treatment with valproate, lamotrigine, and topiramate and the prognosis of the idiopathic generalised epilepsies.

Absence and myoclonic status epileptucus precipitated by antiepileptic drugs in idiopathic generalized epilpesy.

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Juvenile myoclonic epilepsy

These events typically occur either early in the morning or upon sleep deprivation. Additional clinical presentations include seizures with either a motor tonic-clonic seizure or nonmotor absence seizure generalized onset. The characteristic signs of JME are brief episodes of involuntary muscle twitching. These are brief episodes of involuntary muscle contractions occurring early in the morning or shortly before falling asleep. They are more common in the arms than in the legs and may result in dropping objects. Myoclonic jerks may as well appear in clusters.

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