Progressive Myoclonus Epilepsy (Lafora Type)
The diagnosis of Lafora's syndrome, progressive myoclonus epilepsy and intracytoplasmic periodic acid-Schiff-positive inclusions (Lafora bodies), was made by skin biopsy in a 16-year-old girl at the Depts of Pathology and Dermatology, University of Texas Medical Branch, Galveston, TX.
Saved in:
Main Author: | J Gordon Millichap (Author) |
---|---|
Format: | Book |
Published: |
Pediatric Neurology Briefs Publishers,
1988-01-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Laforin targets malin to glycogen in Lafora progressive myoclonus epilepsy
by: Sharmistha Mitra, et al.
Published: (2023) -
Myoclonus Epilepsies
by: J Gordon Millichap
Published: (1990) -
Genetics of Unverricht-Lundborg Myoclonus Epilepsy
by: J Gordon Millichap
Published: (1993) -
Pathogenesis of Opsoclonus Myoclonus
by: J Gordon Millichap
Published: (2003) -
Opsoclonus-Myoclonus Outcome
by: J Gordon Millichap
Published: (1995)