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Epilepsies, Myoclonic

Known as: Disorders, Myoclonic Seizure, Seizures, myoclonic, epilepsy myoclonic 
A clinically diverse group of epilepsy syndromes characterized either by myoclonic seizures or by myoclonus in association with other seizure types… Expand
National Institutes of Health

Papers overview

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Review
2005
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… Expand
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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… Expand
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Highly Cited
2001
Highly Cited
2001
Severe myoclonic epilepsy of infancy (SMEI) is a rare disorder that occurs in isolated patients. The disease is characterized by… Expand
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Highly Cited
2000
Highly Cited
2000
BACKGROUND Stiripentol is an inhibitor of cytochrome P450 that showed antiepileptic efficacy in severe myoclonic epilepsy in… Expand
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Highly Cited
1999
Highly Cited
1999
MRI scans of patients with idiopathic generalized epilepsy (IGE) are normal on visual assessment. Using an interactive anatomical… Expand
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Highly Cited
1998
Highly Cited
1998
PURPOSE In severe myoclonic epilepsy of infancy (SME), multiple drug-resistant focal and generalized seizure types occur… Expand
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Highly Cited
1994
Highly Cited
1994
Hereditary dentatorubral–pallidoluysian atrophy (DRPLA) is an autosomal dominant neurologic disorder characterized by variable… Expand
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Highly Cited
1990
Highly Cited
1990
MITOCHONDRIAL encephalomyopathies are usually divided into three distinct clinical subgroups: (1) mitochondrial myopathy… Expand
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Highly Cited
1984
Highly Cited
1984
We report on two patients who have a mitochondrial myopathy, encephalopathy, lactic acidosis, and recurrent cerebral insults that… Expand
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