Results 141 to 150 of about 1,010 (187)
Some of the next articles are maybe not open access.

In Vivo Kinetics of [18F](N-Methyl)Benperidol: A Novel PET Tracer for Assessment of Dopaminergic D2-Like Receptor Binding

Journal of Cerebral Blood Flow and Metabolism, 1997
S. Moerlein   +3 more
semanticscholar   +1 more source

Pharmacokinetics of benperidol in volunteers after oral administration.

International journal of clinical pharmacology research, 1988
Benperidol in a 4 mg single dose was administered orally to five healthy male volunteers. The drug was rapidly absorbed (tmax = 2.27 +/- 0.57 h) and largely distributed, the volume of distribution being 5.19 +/- 1.99 l.kg-1. Elimination half-life was 7.65 +/- 2.14 h. Urinary excretion represented only a minimal fraction of ingested dose (0.1 +/- 0.007%)
M, Furlanut   +5 more
openaire   +1 more source

Benperidol

2010
Peter J. Tyrer   +81 more
openaire   +2 more sources

In vivo saturation binding analysis using small animal PET - the impact of the reference tissue on the binding potential of [18F]N-methyl-benperidol

IEEE Nuclear Science Symposium Conference Record, 2008
S. Nikolaus   +5 more
semanticscholar   +1 more source

PLASMA LEVELS OF NEUROLEPTIC DRUG AND PROLACTIN AFTER ACUTE DOSES OF BENPERIDOL

Clinical Neuropharmacology, 1992
Ch. Hiemke   +5 more
openaire   +2 more sources

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