Movement Disorders (revue)

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Therapeutic trial of milacemide in patients with myoclonus and other intractable movement disorders

Identifieur interne : 005D11 ( Main/Exploration ); précédent : 005D10; suivant : 005D12

Therapeutic trial of milacemide in patients with myoclonus and other intractable movement disorders

Auteurs : Mark Forrest Gordon [États-Unis] ; Rolando Diaz-Olivo [États-Unis] ; Ann L. Hunt [États-Unis] ; Fahn [États-Unis]

Source :

RBID : ISTEX:4D6408861423607BD4C2335834D9A2AD0E49505A

Descripteurs français

English descriptors

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 X‐linked dystonia with parkinsonism, painful legs and moving toes, and stiff‐person 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 clear‐cut observable improvement occurred. There were no serious adverse effects.

Url:
DOI: 10.1002/mds.870080412


Affiliations:


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Le document en format XML

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<term>Aged</term>
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<div type="abstract" xml:lang="en">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 X‐linked dystonia with parkinsonism, painful legs and moving toes, and stiff‐person 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 clear‐cut observable improvement occurred. There were no serious adverse effects.</div>
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