Myoclonic epilepsy in infancy: An electroclinical study and long‐term follow‐up of 38 patients

Roberto Caraballo, Santiago Flesler, María Constanza Pasteris, María Francisca Lopez Avaria, Sebastián Fortini, Carolina Vilte

Epilepsia · 2013 · 36 citations · 25 references

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Abstract

MEI is a well-defined epileptic syndrome of unknown etiology, but likely of a genetic cause. It is self-limited and pharmacosensitive mainly to valproic acid.

References

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