Search Results - "Kleef, U W"

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  1. 1

    Hepatobiliary disposition of vecuronium bromide in man by Bencini, A F, Scaf, A H, Sohn, Y J, Kersten-Kleef, U W, Agoston, S

    Published in British journal of anaesthesia : BJA (01-09-1986)
    “…The plasma and bile concentrations, the biliary excretion and the neuromuscular blocking effect of vecuronium bromide were studied during surgery in 13…”
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  2. 2

    Do plasma concentrations obtained from early arterial blood sampling improve pharmacokinetic/pharmacodynamic modeling? by Beaufort, T M, Proost, J H, Kuizenga, K, Houwertjes, M C, Kleef, U W, Wierda, J M

    “…In pharmacokinetic/pharmacodynamic (PK/PD) modeling the first blood sample is usually taken 1 to 2 min after drug administration (late sampling). Therefore,…”
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  3. 3

    The pharmacokinetics, urinary and biliary excretion of pipecuronium bromide by Wierda, J M, Szenohradszky, J, De Wit, A P, Zentai, G, Agoston, S, Kakas, M, Kleef, U W, Meijer, D K

    Published in European journal of anaesthesiology (01-11-1991)
    “…The pharmacodynamics and -kinetics of pipecuronium were studied in 12 patients, six of whom received 100 micrograms kg-1 for laryngectomy (Group L), and six…”
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  4. 4

    Pharmacokinetics and Pharmacodynamics of Pipecuronium in Patients with Cirrhosis by DʼHonneur, G., Khalil, M., Dominique, C., Haberer, J. P., Kleef, U. W., Duvaldestin, P.

    Published in Anesthesia and analgesia (01-12-1993)
    “…To determine the effect of liver cirrhosis on the pharmacokinetics and pharmacodynamics of pipecuronium, the authors administered 100 μg/kg of pipecuronium…”
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  5. 5

    The pharmacodynamics and pharmacokinetics of Org 9426, a new non-depolarizing neuromuscular blocking agent, in patients anaesthetized with nitrous oxide, halothane and fentanyl by MARK, J, WIERDA, K. H, KLEEF, U. W, LAMBALK, L. M, KLOPPENBURG, W. D, AGOSTON, S

    Published in Canadian journal of anesthesia (01-05-1991)
    “…The pharmacodynamics and pharmacokinetics of a new non-depolarizing neuromuscular blocking agent, Org 9426, were investigated. Ten patients undergoing elective…”
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  6. 6

    Preliminary investigations of the clinical pharmacology of three short-acting non-depolarizing neuromuscular blocking agents, Org 9453, Org 9489 and Org 9487 by WIERDA, J. M. K. H, BEAUFORT, A. M, KLEEF, U. W, SMEULERS, N. J, AGOSTON, S

    Published in Canadian journal of anesthesia (01-03-1994)
    “…Three muscle relaxants, Org 9453, Org 9489 and Org 9487, short-acting in animals, were investigated to establish their profiles in humans. Potency, time course…”
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  7. 7

    Determination of rocuronium and its putative metabolites in body fluids and tissue homogenates by Kleef, U W, Proost, J H, Roggeveld, J, Wierda, J M

    Published in Journal of chromatography (17-11-1993)
    “…A sensitive and selective HPLC method was developed for the quantification of the neuromuscular blocking agent rocuronium and its putative metabolites (the…”
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  8. 8

    The influence of hypothermia (surface cooling) on the time-course of action and on the pharmacokinetics of rocuronium in humans by Beaufort, A M, Wierda, J M, Belopavlovic, M, Nederveen, P J, Kleef, U W, Agoston, S

    “…Hypothermia prolongs the time-course of action of non-depolarizing neuromuscular blocking agents. The mechanism, however, is unknown. We studied the influence…”
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  9. 9

    Pharmacokinetics and cardiovascular dynamics of pipecuronium bromide during coronary artery surgery by WIERDA, J. M. K. H, KARLICZEK, G. F, VANDENBROM, R. H. G, PINTO, I, KERSTEN-KLEEF, U. W, MEIJER, D. K. F, AGOSTON, S

    Published in Canadian journal of anesthesia (01-03-1990)
    “…The haemodynamic effects of 200 micrograms.kg-1 pipecuronium and pancuronium were compared under etomidate/piritramide anaesthesia in 20 patients scheduled for…”
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  10. 10

    The isolated heart-lung preparation in the cat. An in situ model to study the role of the lungs in the disposition of drugs by Beaufort, A M, Wierda, J M, Houwertjes, M C, Kleef, U W, Meijer, D K

    “…In the search for drugs with an extreme short time course of action, compounds should be developed that are rapidly distributed to and temporarily stored in…”
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  11. 11