We investigated the therapeutic effects of milacemide in seven patients with myoclonus and three patients with the stiff-person syndrome in an open-label trial. Milacemide was initiated at 800 mg/day and was gradually increased to a maximum dosage of 2,400 mg/day. No significant improvement occurred
Therapeutic trial of milacemide in patients with myoclonus and other intractable movement disorders
โ Scribed by Mark Forrest Gordon; Rolando Diaz-Olivo; Ann L. Hunt; Dr. Stanley Fahn
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- English
- Weight
- 478 KB
- Volume
- 8
- Category
- Article
- ISSN
- 0885-3185
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โฆ Synopsis
Abstract
We performed a therapeutic trial with the glycine precursor, milacemide, on 10 patients with intractable movement disorders. Six had myoclonus of various etiologies and one each had progressive supranuclear palsy, Filipino Xโlinked dystonia with parkinsonism, painful legs and moving toes, and stiffโperson syndrome. Milacemide was initiated at a dose of 2,400 mg/ day, orally, and increased gradually to a maximum of 4,800 mg/ day. No clearโcut observable improvement occurred. There were no serious adverse effects.
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