Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Jma van Gerven"'
Autor:
S Brooks, RGJA Zuiker, C Bleys, D Ziagkos, JA Moyer, L van Nueten, P Bonaventure, WC Drevets, JMA van Gerven, G Salvadore, GE Jacobs
Publikováno v:
Journal of Psychopharmacology. :026988112311679
Background: Up to 40% of patients suffering from anxiety disorders do not benefit from currently available pharmacological treatments. Overactivity of the orexin-1 receptor (OX1R) has been implicated in anxiety- and panic-related states. Aim & method
Autor:
Rik C. Schoemaker, J. den Hartigh, Adam F. Cohen, Jean-Louis Pinquier, Lineke Zuurman, Jcme Bender, Arno Hazekamp, C. Roy, Robert Verpoorte, Jma van Gerven
Publikováno v:
Journal of Psychopharmacology. 22:707-716
This randomised, double-blind, placebo-controlled, cross-over study was designed to identify which pharmacodynamic parameters most accurately quantify the effects of delta-9-Tetrahydrocannabinol (THC), the predominantly psychoactive component of cann
Autor:
Gabriel E. Jacobs, Imc Kamerling, J. van Pelt, Frans G. Zitman, Jma van Gerven, Roel H. DeRijk, ML de Kam
Publikováno v:
Journal of Psychopharmacology, 24(1), 65-72
A recently developed oral serotonergic challenge test consisting of 5-Hydroxytryptophane (5-HTP, 200 mg) combined with carbidopa (CBD, 100 mg + 50 mg) exhibited dose-related neuroendocrine responsiveness and predictable pharmacokinetics. However, its
Publikováno v:
Journal of Psychopharmacology. 23:633-644
Abstract CB1/CB2 agonists are reported to have sedative, amnestic, analgesic and anti-emetic properties, which would make them ideal drugs for outpatient treatments under conscious sedation. The main objective of this in human study was to assess the
Autor:
R.H. de Rijk, J. P. Van Der Post, Gabriel E. Jacobs, Rik C. Schoemaker, J. van Pelt, Dhm Hoeberechts-Lefrandt, Ljca Smarius, ML de Kam, Jma van Gerven, Harm J. Gijsman, Frans G. Zitman
Publikováno v:
Journal of Psychopharmacology. 22:426-433
5-hydroxytryptophan (5-HTP) is a direct 5-hydroxytryptamine (5-HT) precursor used to assess central serotonergic function. Its use has been limited by a narrow window between neuroendocrine changes and side effects, and variable kinetics related to i
Autor:
Rwm Zoethout, Adam F. Cohen, K Van Dyck, Rik C. Schoemaker, M De Smet, SL de Haas, Keith Gottesdiener, Laura B. Rosen, M. G Murphy, Jma van Gerven
Publikováno v:
Journal of Psychopharmacology, 26(2), 282-91
Journal of Psychopharmacology, 26(2), 282-291
Journal of Psychopharmacology, 26(2), 282-291
Essential tremor (ET) is a relatively frequent neurological disorder that responds in some patients to gamma-aminobutyric acid A (GABAA) agonists such as the benzodiazepines. Partial subtype-selective GABAA agonists may have an improved side effect p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2424821892ee6db823ed48ff5e13f25
http://hdl.handle.net/1887/118587
http://hdl.handle.net/1887/118587
Autor:
A Andorn, Erica S. Klaassen, Paolo Fina, L Iavarone, Jma van Gerven, Msg Bani, Rwm Zoethout, E.T. te Beek
Publikováno v:
Journal of Psychopharmacology, 26(2), 303-314
GSK598809 is a novel selective dopamine D3 receptor antagonist, currently in development for the treatment of substance abuse and addiction. In a blinded, randomized, placebo-controlled study, effects of single oral doses of 175 mg GSK598809 were eva
Autor:
Mark E. Schmidt, Rwm Zoethout, Marieke Liem-Moolenaar, Jma van Gerven, P. De Boer, ML de Kam, Adam F. Cohen, Kari L. Franson
Publikováno v:
Journal of psychopharmacology (Oxford, England). 24(11)
In this study the effects of R213129, a selective glycine transporter 1 inhibitor, on central nervous system function were investigated in healthy males in the absence and presence of scopolamine. This was a double-blind, placebo-controlled, 4-period
Autor:
Jaj Schmitt, S. J. De Visser, Marieke Liem-Moolenaar, Adam F. Cohen, Kari L. Franson, Jma van Gerven, Rik C. Schoemaker, Frank A Gray
Publikováno v:
Journal of Psychopharmacology, 24(1), 73-82
Central Nervous System (CNS) effects of talnetant, an NK-3 antagonist in development for schizophrenia, were compared to those of haloperidol and placebo. The study was randomised, double-blind, three-way crossover of talnetant 200 mg, haloperidol 3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fdaae5283614134054a075cc75a117f7
https://hdl.handle.net/1887/119182
https://hdl.handle.net/1887/119182
Autor:
Rik C. Schoemaker, J.G. van Dijk, Maarten J. Titulaer, ML de Kam, Jma van Gerven, Jan J.G.M. Verschuuren, Paul W. Wirtz, UR Tjaden, Jgc van Hasselt, J. den Hartigh
Publikováno v:
Clinical pharmacology and therapeutics. 86(1)
3,4-Diaminopyridine and pyridostigmine are widely used to treat Lambert-Eaton myasthenic syndrome (LEMS), either alone or in combination. 3,4-Diaminopyridine enhances the release of acetylcholine at the neuromuscular synapse, and pyridostigmine inhib