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1 pears to be efficacious for nonresponders to nefazodone, and nefazodone appears to be effective for C
3 RI) antidepressants (bupropion, mirtazapine, nefazodone, and venlafaxine), tricyclic antidepressants,
4 cacious for nonresponders to nefazodone, and nefazodone appears to be effective for CBASP nonresponde
6 the rates of response were 55 percent in the nefazodone group and 52 percent in the psychotherapy gro
8 factory response) was 48 percent in both the nefazodone group and in the psychotherapy group, as comp
10 new-generation non-SSRI antidepressants (eg, nefazodone hydrochloride, mirtazapine, bupropion hydroch
12 der to 12 weeks of outpatient treatment with nefazodone (maximal dose, 600 mg per day), the cognitive
14 lopram, fluoxetine, imipramine, mirtazapine, nefazodone, nortriptyline, paroxetine, sertraline, and v
15 response to short-term treatment with either nefazodone or a cognitive behavioral-analysis system of
16 ater risks of hepatotoxicity are iproniazid, nefazodone, phenelzine, imipramine, amitriptyline, dulox
17 e to CBASP and the switch from from CBASP to nefazodone resulted in clinically and statistically sign
19 mistries should be performed before starting nefazodone therapy and patients should be monitored regu
20 temporal onset of disease after the start of nefazodone therapy suggested severe hepatocellular injur
22 at sample revealed that both the switch from nefazodone to CBASP and the switch from from CBASP to ne
23 ts (selective serotonin reuptake inhibitors, nefazodone, venlafaxine, and mirtazapine) in participant
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