Progressive myoclonus epilepsies: specific causes and diagnosis

N Engl J Med. 1986 Jul 31;315(5):296-305. doi: 10.1056/NEJM198607313150506.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Adolescent
  • Adult
  • Biopsy
  • Brain / pathology
  • Central Nervous System Diseases / complications
  • Child
  • Child, Preschool
  • Epilepsies, Myoclonic / diagnosis*
  • Epilepsies, Myoclonic / drug therapy
  • Epilepsies, Myoclonic / etiology
  • Galactosidases / deficiency
  • Humans
  • Metabolism, Inborn Errors / complications
  • Middle Aged
  • Mitochondria / ultrastructure
  • Myoclonic Cerebellar Dyssynergia / complications
  • Myoclonic Cerebellar Dyssynergia / diagnosis
  • Neuraminidase / deficiency
  • Neuronal Ceroid-Lipofuscinoses / complications
  • Neuronal Ceroid-Lipofuscinoses / diagnosis

Substances

  • Galactosidases
  • Neuraminidase