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Myoclonic Epilepsy, Juvenile

Known as: Myoclonic Epilepsy, Juvenile, 1, Impulsive Petit Mal, Janz, Myoclonic Epilepsies, Adolescent 
A disorder characterized by the onset of myoclonus in adolescence, a marked increase in the incidence of absence seizures (see EPILEPSY, ABSENCE… 
National Institutes of Health

Papers overview

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Highly Cited
2016
Highly Cited
2016
In contrast to plant-animal interactions, the conceptual framework regarding the impact of secondary metabolites in mediating… 
Highly Cited
2004
Highly Cited
2004
Juvenile myoclonic epilepsy (JME) is the most frequent cause of hereditary grand mal seizures. We previously mapped and narrowed… 
Highly Cited
2004
Highly Cited
2004
Damage to the orbitofrontal cortex (OFC) in humans has been associated with disinhibited or socially inappropriate behaviour and… 
Highly Cited
2002
Highly Cited
2002
Although many genes that predispose for epilepsy in humans have been determined, those that underlie the classical syndromes of… 
Highly Cited
1997
Highly Cited
1997
Neuronal apoptosis was observed in the rat dentate gyrus in two experimental models of human limbic epilepsy. Five hours after… 
Review
1996
Review
1996
DIAGNOSTIC ACCURACY AND CASE FINDING Accurate diagnostic and case ascertainment methods are a prerequisite for epidemiological… 
Highly Cited
1994
Highly Cited
1994
The neuromodulator serotonin (5-hydroxytryptamine, 5-HT) has been associated with mood disorders such as depression, anxiety, and… 
Review
1985
Review
1985
ABSTRACT – Juvenile myoclonic epilepsy (JME) is a special syndrome within the primary generalized epilepsies which is… 
Highly Cited
1984
Highly Cited
1984
We studied 43 patients, aged 15 to 69 years, whose convulsive seizures were uncontrolled because the syndrome of juvenile… 
Highly Cited
1980
Highly Cited
1980
Bulimia is a poor prognostic sign in anorexia nervosa. This raised the question of whether bulimia represented an "end stage" of…