Epileptic seizures and electroencephalographic evolution in genetic leukodystrophies

Journal of Clinical Neurophysiology

Volumn 18, Issue 1, 2001, Pages 25-32

  Wang, Pen Jung ^a,b   Hwu, Whu Liang ^a   Shen, Yu Zen ^a  

^a NATIONAL TAIWAN UNIVERSITY HOSPITAL   (Taiwan)

^b TZU CHI UNIVERSITY   (Taiwan)

Author keywords

EEG; Epilepsy; Evolution; Genetic leukodystrophies; Seizures

Indexed keywords

ADOLESCENT; ADRENOLEUKODYSTROPHY; ARTICLE; CHILD; CLINICAL ARTICLE; DISEASE COURSE; DISEASE SEVERITY; ELECTROENCEPHALOGRAPHY; GLOBOID CELL LEUKODYSTROPHY; GRAY MATTER; HUMAN; INTRACTABLE EPILEPSY; LEUKODYSTROPHY; METACHROMATIC LEUKODYSTROPHY; NUCLEAR MAGNETIC RESONANCE IMAGING; PELIZAEUS MERZBACHER DISEASE; SEIZURE; WHITE MATTER;

EID: 0035085733     PISSN: 07360258     EISSN: None     Source Type: Journal    
DOI: 10.1097/00004691-200101000-00006     Document Type: Article

References (22)

1. Recurrent seizures in metachromatic leukodystrophy
2. EEG findings in late infantile metachromatic and globoid cell leukodystrophy
3. The electroencephalogram in diffuse encephalopathies: Electroencephalographic correlates of gray and white matter lesion
4. Connatal Pelizaeus-Merzhacher disease
5. Clinical symptoms, signs and tests in metachromatic leukodystrophy
6. Infantile globoid cell leukodystrophy (Krabbe's disease): A clinical and genetic study of 32 Swedish cases 1953-1967
7. Inhibition of cytochrome c oxidase by psychosine (galactosylsphingosine)
8. Lipids of developing brain of twitcher mouse - An authentic murine model of human Krabbe disease
9. A duplication of PLP gene causing Pelizaeus-Merzbacher disease detected by comparative multiplex PCR
10. Neonatal adrenoleukodystrophy: Clinical, pathologic and biochemical delineation of a syndrome affecting both males and females
11. Some EEG observations in patients with Krabbe's disease
12. Electroencephalography in diffuse encephalopathies
13. Cerebro-hepato-renal (Zellweger) syndrome, adrenoleukodystrophy, and Refusum's disease: Plasma changes and skin fibroblast phytanic acid oxidase
14. Epilepsy in peroxisomal diseases
15. Multiple peroxisomal enzymatic deficiency disorders. A comparative biochemical and morphologic study of Zellweger cerebrohepatorenal syndrome and neonatal adrenoleukodystrophy
16. The reflection of history in MR imaging of Pelizaeus-Merzbacher disease
17. Electrophysiologic studies in neonatal adrenoleukodystrophy
18. Neonatal adrenoleukodystrophy: Impaired plasmalogen biosynthesis and peroxisomal β-oxidation due to a deficiency of catalase-containing particles (peroxisomes) in cultured skin fibroblasts
19. Duplication of proteolipid protein gene: A possible major cause of Pelizaeus-Merzbacher disease
20. A study of genetic leukodystrophies in Chinese children
21. Electrophysiologic observation in the classic form of Pelizaeus-Merzbacher disease
22. Pelizaeus-Merzbacher disease. Identification of Xq 22 proteolipid-protein duplication and characterization of breakpoints by interphase FISH