Article
Familial Unverricht-Lundborg disease: a clinical, neurophysiologic, and genetic study.
Epilepsia - 1 Jun 1997
Parmeggiani A, Lehesjoki A E, Carelli V, Posar A, Santi A, Santucci M, Gobbi G, Pini A, Rossi P G
Abstract excerpt
PURPOSE: Progressive myoclonus epilepsies (PMEs) are a clinically and etiologically heterogeneous group of disorders. The authors report clinical, neurophysiological, and genetic findings of a family from Southern Italy with three members affected with PME. METHODS: All data about familial and personal antecedents, clinical history, neurologic examination, laboratory tests, neurophysiological findings, brain...
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