A therapeutic trial of milacemide in myoclonus and the stiff‐person syndrome
Identifieur interne : 006203 ( Main/Exploration ); précédent : 006202; suivant : 006204A therapeutic trial of milacemide in myoclonus and the stiff‐person syndrome
Auteurs : P. Brown [Royaume-Uni] ; P. D. Thompson [Royaume-Uni] ; J. C. Rothwell [Royaume-Uni] ; B. L. Day [Royaume-Uni] ; Marsden [Royaume-Uni]Source :
- Movement Disorders [ 0885-3185 ] ; 1991.
Descripteurs français
- Pascal (Inist)
- Wicri :
- topic : Homme.
English descriptors
- KwdEn :
- Acetamides (therapeutic use), Adult, Aged, Anticonvulsants, Chemotherapy, Female, Glycine, Human, Humans, Involuntary movement, Male, Middle Aged, Milacemide, Monoamine Oxidase Inhibitors, Muscle Rigidity (drug therapy), Myoclonus, Myoclonus (drug therapy), Nervous system diseases, Neurologic Examination, Precursor, Spasm (drug therapy), Stiff man syndrome, Stiff‐person syndrome, Striated muscle disease, Syndrome, Treatment.
- MESH :
- chemical , therapeutic use : Acetamides.
- drug therapy : Muscle Rigidity, Myoclonus, Spasm.
- Adult, Aged, Anticonvulsants, Female, Humans, Male, Middle Aged, Monoamine Oxidase Inhibitors, Neurologic Examination, Syndrome.
Abstract
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 in the 10 patients.
Url:
DOI: 10.1002/mds.870060114
Affiliations:
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Le document en format XML
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<term>Adult</term>
<term>Aged</term>
<term>Anticonvulsants</term>
<term>Chemotherapy</term>
<term>Female</term>
<term>Glycine</term>
<term>Human</term>
<term>Humans</term>
<term>Involuntary movement</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Milacemide</term>
<term>Monoamine Oxidase Inhibitors</term>
<term>Muscle Rigidity (drug therapy)</term>
<term>Myoclonus</term>
<term>Myoclonus (drug therapy)</term>
<term>Nervous system diseases</term>
<term>Neurologic Examination</term>
<term>Precursor</term>
<term>Spasm (drug therapy)</term>
<term>Stiff man syndrome</term>
<term>Stiff‐person syndrome</term>
<term>Striated muscle disease</term>
<term>Syndrome</term>
<term>Treatment</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="therapeutic use" xml:lang="en"><term>Acetamides</term>
</keywords>
<keywords scheme="MESH" qualifier="drug therapy" xml:lang="en"><term>Muscle Rigidity</term>
<term>Myoclonus</term>
<term>Spasm</term>
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<keywords scheme="MESH" xml:lang="en"><term>Adult</term>
<term>Aged</term>
<term>Anticonvulsants</term>
<term>Female</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Monoamine Oxidase Inhibitors</term>
<term>Neurologic Examination</term>
<term>Syndrome</term>
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<keywords scheme="Pascal" xml:lang="fr"><term>Chimiothérapie</term>
<term>Glycine</term>
<term>Homme</term>
<term>Homme raide syndrome</term>
<term>Milacémide</term>
<term>Mouvement involontaire</term>
<term>Muscle strié pathologie</term>
<term>Myoclonie</term>
<term>Précurseur</term>
<term>Système nerveux pathologie</term>
<term>Traitement</term>
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<front><div type="abstract" xml:lang="en">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 in the 10 patients.</div>
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<name sortKey="Day, B L" sort="Day, B L" uniqKey="Day B" first="B. L." last="Day">B. L. Day</name>
<name sortKey="Marsden" sort="Marsden" uniqKey="Marsden" last="Marsden">Marsden</name>
<name sortKey="Rothwell, J C" sort="Rothwell, J C" uniqKey="Rothwell J" first="J. C." last="Rothwell">J. C. Rothwell</name>
<name sortKey="Thompson, P D" sort="Thompson, P D" uniqKey="Thompson P" first="P. D." last="Thompson">P. D. Thompson</name>
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