Results 311 to 320 of about 74,631 (338)
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Determination of Purity of Levodopa and Levodopa Products by GLC

Journal of Pharmaceutical Sciences, 1974
A simple GLC procedure for the detection and quanti-tation of possible impurities in levodopa raw material and commercial dosage forms is presented. The sample is reacted with N,O-bis(trimethylsilyl)acetamide in acetonitrile at ambient temperature for 30 min, and the silyl derivatives are separated on a methyl silicone column under isothermal ...
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Is levodopa toxic?

Neurology, 1996
Shortly after the introduction of high-dosage levodopa for the treatment of Parkinson's disease (PD), adverse motor effects of dyskinesias and clinical fluctuations ("wearing-off" and "on-off" phenomena) were seen [see [1] for historical review]. This soon led to the suggestion [2] that the introduction of levodopa for the treatment of PD should be ...
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Comparison of Levodopa with Carbidopa, and Levodopa with Domperidone in Parkinsonʼs Disease

Clinical Neuropharmacology, 1986
In a comparison of the effects of domperidone and carbidopa during levodopa treatment, 20 patients with idiopathic Parkinson's disease were treated with fixed dose regimens of either levodopa 500 mg-domperidone 20 mg or levodopa 100 mg-carbidopa 25 mg; each for 8 weeks.
J D Parkes, P N Malcolm, N Langdon
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Levodopa

Neurology, 1998
Whether a drug such as levodopa, which is prescribed for long periods, may be toxic is a legitimate and even indispensable question. The problem is no different from that posed by other drugs-such as calcium antagonists, antihypertensives, or hormones-normally prescribed for chronic diseases. What, however, is meant in this context by "toxic" (from the
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Pharmacokinetics and pharmacodynamics of levodopa

Movement Disorders, 2008
The pharmacokinetics and pharmacodynamics of levodopa are dominated by two features: the short plasma half-life of the drug and the portion of the antiparkinsonian response that parallels the plasma levodopa levels, the so-called short-duration response. These features are the basis of motor fluctuations that complicate long-term therapy with levodopa.
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LEVODOPA IN HEPATIC COMA

The Lancet, 1970
Abstract Five patients with acute hepatic failure in coma or stupor were given drugs affecting neurotransmission. Levodopa (L-dopa) produced in three patients a striking though temporary improvement in the level of consciousness together with striking improvement in the previously abnormal electroencephalographic (E.E.G.) recordings.
J. D. Parkes   +2 more
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LEVODOPA AND MIGRAINE

The Lancet, 1970
AntónioR Damásio   +2 more
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Levodopa and Alcoholism

JAMA: The Journal of the American Medical Association, 1975
To the Editor.— A variety of animal 1,2 and human 3 experiments have suggested that neural transmitters may mediate some of the symptoms of alcohol intoxication and withdrawal. Also, there is evidence to suggest that a dopamine agonist (apomorphine) reduces craving for alcohol in human alcoholics 4 and ethanol stimulation in mice.
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Pharmacokinetics of Levodopa

Clinical Neuropharmacology, 1984
J H Fellman, John G. Nutt
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