Absences in juvenile myoclonic epilepsy: A clinical and video-electroencephalographic study
β Scribed by Dr. Chrysostomos P. Panayiotopoulos; Tahir Obeid; Ghazala Waheed
- Publisher
- John Wiley and Sons
- Year
- 1989
- Tongue
- English
- Weight
- 732 KB
- Volume
- 25
- Category
- Article
- ISSN
- 0364-5134
No coin nor oath required. For personal study only.
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We recently analyzed under homogeneity a large pedigree from Belize with classic juvenile myoclonic epilepsy (JME). After a genome wide search with 146 microsatellites, we obtained significant linkage between chromosome 6p markers, D6S257 and D6S272, and both convulsive and EEG traits of JME. Recomb
Juvenile myoclonic epilepsy (JME) is not an uncommon seizure disorder, occurring in 5-10% of epileptic patients. A subclinical anterior horn cell involvement has been suggested in some JME patients by concentric needle electromyography (EMG) and turn/amplitude analysis. In this study, 22 JME patient
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