Abstract
Eight patients with dystonia, four with hereditary torsion dystonia and four with acquired dystonia, were treated with carbamazepine in doses ranging from 300 to 1,200 mg/day. Drowsiness was the only side effect and periodic blood cell counts remained normal. All have shown sustained improvement of some manifestations of their illness for periods up to one year.
| Original language | English |
|---|---|
| Pages (from-to) | 1755-1757 |
| Number of pages | 3 |
| Journal | JAMA |
| Volume | 229 |
| Issue number | 13 |
| DOIs | |
| State | Published - 23 Sep 1974 |
| Externally published | Yes |
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