Epilepsy in Juvenile Neuronal Ceroid Lipofuscinosis
The clinical characteristics of epilepsy and optimal antiepileptic drug therapy were surveyed in 60 patients (mean age 16 years, range 5-33) with juvenile neuronal ceroid lipofuscinosis (JNCL), followed at the University of Helsinki, Finland.
Saved in:
Main Author: | J Gordon Millichap (Author) |
---|---|
Format: | Book |
Published: |
Pediatric Neurology Briefs Publishers,
2000-10-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Subdural Effusion and Infantile Neuronal Ceroid Lipofuscinosis
by: J Gordon Millichap
Published: (2010) -
EEG in Late Infantile Neuronal Ceroid Lipofuscinosis
by: J Gordon Millichap
Published: (2001) -
Spino-Cerebellar Degeneration and Ceroid Lipofuscinosis
by: J Gordon Millichap
Published: (1988) -
Neuronal ceroid lipofuscinosis and Bardet-Biedl syndrome in patient with retinitis pigmentosa
by: José D. Santotoribio, et al.
Published: (2021) -
Immunomodulation with minocycline rescues retinal degeneration in juvenile neuronal ceroid lipofuscinosis mice highly susceptible to light damage
by: Katharina Dannhausen, et al.
Published: (2018)