Carregant...

Posterior paroxysmal discharge: an aid to early diagnosis in Lafora disease.

Lafora body disease is a rare neurometabolic disorder of autosomal recessive inheritance. Symptoms begin in the second decade with progressive myoclonic epilepsy and survival is unusual beyond the age of 30. We report an electroencephalographic study in four cases of histologically proven Lafora bod...

Descripció completa

Guardat en:
Dades bibliogràfiques
Autors principals: Ponsford, S, Pye, I F, Elliot, E J
Format: Artigo
Idioma:Inglês
Publicat: 1993
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC1294141/
https://ncbi.nlm.nih.gov/pubmed/8230063
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!