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Myoclonic Encephalopathy

Known as: Encephalopathies, Myoclonic, Encephalopathy, Myoclonic, Myoclonic Encephalopathies 
National Institutes of Health

Papers overview

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Review
2005
Review
2005
Despite the fact that there are many descriptions of the pathophysiology of myoclonic seizures, and some clear descriptions of… 
Review
2001
Review
2001
INTRODUCTION The severe epileptic syndromes of infancy are dependent on age, symptomatic or cryptogenic aetiology and are drug… 
Review
1998
Review
1998
CASE REPORT A 39-year-old man ingested 35 g carisoprodol. He developed agitation, tachycardia, myoclonus, and coma. The blood… 
Review
1995
Review
1995
ENM is an etiologically heterogeneous disorder clinically evident as brief (less than 500 msec) lapses of tonic muscular… 
Highly Cited
1993
Highly Cited
1993
Five patients with partial epilepsy of diverse etiology insidiously developed action-activated jerks. The disorder was limited to… 
Review
1990
Review
1990
acute myoclonic encephalopathies,' 2 whose main cause is aluminium overload. This overload results from the use of phosphate… 
1982
1982
Two cases of Lance-Adams syndrome with anatomopathologic study are reported. There were evidences of diffuse neuronal…