Serveur d'exploration sur la maladie de Parkinson

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Lisuride in parkinsonism

Identifieur interne : 002B48 ( Main/Exploration ); précédent : 002B47; suivant : 002B49

Lisuride in parkinsonism

Auteurs : J. D. Parkes ; M. Schachter ; C. D. Marsden ; B. Smith [Royaume-Uni] ; A. Wilson [Royaume-Uni]

Source :

RBID : ISTEX:DCB36F727167E48678FBBB1D49222B1BA5A191A8

Abstract

Lisuride is a soluble ergolene derivative with endocrine effects similar to but more potent than those of bromocriptine. In nine subjects with idiopathic, postencephalitic, or drug‐induced parkinsonism, lisuride at a dosage of 0.05 to 0.15 mg intravenously caused an immediate improvement in tremor, rigidity, akinesia, and postural deformity, but also caused chorea and orofacial dyskinesia. Improvement lasted 2 to 3 hours. Lisuride had little or no effect in a single patient with progressive supranuclear palsy. Oral lisuride therapy, 0.8 to 4.8 mg daily, had similar effects but occasionally caused reduced awareness and hallucinations.

Url:
DOI: 10.1002/ana.410090109


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

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