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Neurophysiology of juvenile myoclonic epilepsy

Epilepsy & Behavior, 2013
Juvenile myclonic epilepsy (JME) can be firmly diagnosed by a careful interview of the patient focusing on the seizures and by the EEG with the help, if necessary, of long-term video-EEG monitoring using sleep and/or sleep deprivation. Background activity is normal. The interictal EEG shows diffuse or generalized spike-wave (SW) and polyspike-wave (PSW)
Rubboli, Guido   +4 more
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The history of juvenile myoclonic epilepsy

Epilepsy & Behavior, 2013
Juvenile myoclonic epilepsy (JME) has been the subject of intensive research over the past 25years. It was discovered stepwise in Switzerland and France in the 19th century, adequately described in Germany and Uruguay in the 1950s, and rediscovered in North America in the early 1980s.
Pierre, Genton, Philippe, Gelisse
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Severe myoclonic epilepsy of infancy

Pediatric Neurology, 1987
Severe myoclonic epilepsy of infancy (SMEI) is a recently identified seizure disorder with a uniformly poor prognosis. No successful therapy has been found for this disorder. Based on the treatment of 7 patients who qualified for the diagnosis in this report, SMEI has a better prognosis than recognized currently.
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Review: Juvenile myoclonic epilepsy

Child: Care, Health and Development, 1994
SummaryJuvenile myoclonic epilepsy does not seem to be recognized as often as it should be, accounting as it does for about one in 10 of those with epilepsy. In addition to the myoclonus, absence seizures and tonic‐clonic fits can occur. The interictal EEG shows polyspike and wave discharges, and during the myoclonus, medium to high amplitude 16 Hz ...
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Myoclonic Epilepsies of Childhood

Neuropediatrics, 1971
J, Aicardi, J J, Chevrie
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Prognosis of juvenile myoclonic epilepsy is related to endophenotypes

Seizure: the Journal of the British Epilepsy Association, 2011
Laura Guilhoto, Katia Lin
exaly  

MYOCLONIC EPILEPSY

The Journal of Nervous and Mental Disease, 1940
R. R. Grinker, H. Serota, S. I. Stein
openaire   +1 more source

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