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1 evelopment of 2 as a novel second-generation antipsychotic agent.
2 variant was applied to rodents receiving an antipsychotic agent.
3 uperior therapeutic effects of this atypical antipsychotic agent.
4 several of the criteria for a novel atypical antipsychotic agent.
5 se I clinical trials as a potential atypical antipsychotic agent.
6 estigated as an approach to a novel atypical antipsychotic agent.
7 mplications for understanding the actions of antipsychotic agents.
8 st-generation and several recently-developed antipsychotic agents.
9 , indicating their potential as nonclassical antipsychotic agents.
10 rom monitoring should guide the selection of antipsychotic agents.
11 ffect of race on the use of various atypical antipsychotic agents.
12 nd release and may have potential utility as antipsychotic agents.
13 prepared and evaluated as potential atypical antipsychotic agents.
14 occupancy of striatal dopamine receptors by antipsychotic agents.
15 isdiagnosis and inappropriate treatment with antipsychotic agents.
16 1), were prepared and evaluated as potential antipsychotic agents.
17 cy of four novel, evidence-based targets for antipsychotic agents: a neurokinin (NK(3)) antagonist (S
18 tion may be useful for testing potential new antipsychotic agents and for characterizing neurobiologi
21 rugs is associated with clinical response to antipsychotic agents and the production of extrapyramida
23 (3) receptors targeted by the most effective antipsychotic agents are maximally expressed, could lead
24 stigated the efficacy of lurasidone, a novel antipsychotic agent, as adjunctive therapy with lithium
25 hanges in response to the advent of atypical antipsychotic agents can be understood in the context of
31 e benefits of the continued use of a typical antipsychotic agent following remission from an acute ma
32 ere 18 to 68 years old, were treated with an antipsychotic agent for 6 months or more at a stable dos
33 panel recommendations regarding choice of an antipsychotic agent for schizophrenia differ markedly, b
34 n criteria were >/=18 years old, were taking antipsychotic agents for >/=30 days, and had a body mass
35 receptor affinity comparable to the typical antipsychotic agent haloperidol and a 5-HT2A/D2 ratio co
37 2.89; 95% CI, 1.51 to 5.55; P=0.001), or an antipsychotic agent (hazard ratio, 3.02; 95% CI, 1.34 to
40 ic drugs, by definition, differ from typical antipsychotic agents in producing significantly fewer ex
41 or safety profile compared with conventional antipsychotic agents in terms of extrapyramidal symptoms
42 ilize omega-3, anticonvulsants, and atypical antipsychotic agents in treating specific DSM-5 BPD trai
44 therapeutic profile of atypical over typical antipsychotic agents include 1) simultaneous antagonism
47 schizophrenia treated with certain atypical antipsychotic agents, it remains unclear whether atypica
48 injectable risperidone, a second-generation antipsychotic agent, may improve adherence to treatment
49 to a blinded, comparative trial of the novel antipsychotic agent olanzapine (5-20 mg/d) or the conven
51 uation, and the efficacy of the conventional antipsychotic agent perphenazine appeared similar to tha
52 nuous infusion to examine the effects of the antipsychotic agent RWJ-37796, on striatal activity in h
53 modern psychotropic agents, such as atypical antipsychotic agents, selective serotonin reuptake inhib
54 is response is specific to second-generation antipsychotic agents (SGAs), as first-generation medicat
57 ned with an anxiolytic, mood stabilising, or antipsychotic agent), supportive psychotherapy (often co
58 cinations in schizophrenia are alleviated by antipsychotic agents that inhibit D2 dopamine receptors
59 e 2 diabetes associated with use of selected antipsychotic agents, the authors conducted a new-user c
60 To report the use of a second-generation antipsychotic agent to assist weaning from prolonged mec
61 ferences in mortality risks among individual antipsychotic agents used for treating patients with dem
63 on of treatment with the identified atypical antipsychotic agent was 68.3 +/- 28.9 months (clozapine)
66 t and imaging studies in mice suggested that antipsychotic agents were not confounding the primary fi
71 sses activity consistent with an efficacious antipsychotic agent with less tendency to induce extrapy
72 tial agonists such as 14 may have utility as antipsychotic agents with increased efficacy and decreas
73 ogues (4a,b and 9a, b) to be the most potent antipsychotic agents with large separation between effic
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