Progressive myoclonus epilepsy with Lafora inclusion bodies. II. Studies of ultrastructure.

@article{Odor1967ProgressiveME,
  title={Progressive myoclonus epilepsy with Lafora inclusion bodies. II. Studies of ultrastructure.},
  author={D. L. Odor and R. Janeway and L. Pearce and J. Ravens},
  journal={Archives of neurology},
  year={1967},
  volume={16 6},
  pages={
          583-94
        }
}
Lafora's AFORA'S disease is a rare form of myoclonus epilepsy. 1 It is characterized by myoclonus, generalized convulsions, and progressive mental deterioration which begin during adolescence. Death within four to ten years has been the inevitable outcome in all reported cases. This report describes the ultrastructure of the inclusion bodies found in cerebral cortical biopsy specimens from two patients with Lafora's disease. The ultrastructure of liver and gastrocnemius muscle are also briefly… Expand
PROGRESSIVE MYOCLONIC EPILEPSY WITH LAFORA'S BODIES
Lafora's disease: towards a clinical, pathologic, and molecular synthesis.
Presenile dementia with "Lafora-like" intraneuronal inclusions.
Lafora's disease
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