Chew et al. 1 studied the long-term natural history of Unverricht-Lundborg disease (ULD, progressive myoclonic epilepsy of Unverricht-Lundborg type, EPM1, OMIM #254800) in 8 patients with mutations in the cystatin B gene (CSTB). 1 Working in the area of Southern Sweden where Herman Lundborg (1868-19
Death in Unverricht–Lundborg disease
✍ Scribed by Hela Mrabet Khiari; Silvana Franceschetti; Nebojsa Jovic; Amel Mrabet; Pierre Genton
- Publisher
- Springer Milan
- Year
- 2009
- Tongue
- English
- Weight
- 137 KB
- Volume
- 30
- Category
- Article
- ISSN
- 1590-1874
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Chew et al. 1 studied the long-term natural history of Unverricht-Lundborg disease (ULD, progressive myoclonic epilepsy of Unverricht-Lundborg type, EPM1, OMIM #254800) in 8 patients with mutations in the cystatin B gene (CSTB). 1 Working in the area of Southern Sweden where Herman Lundborg (1868-19
## Abstract Patients with Unverricht–Lundborg disease, also referred to as progressive myoclonus epilepsy type 1, exhibit widespread motor symptoms and signs in addition to epileptic seizures, which suggest abnormal excitability of the primary motor pathways. To explore the plasticity of the sensor
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