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1 r schizophrenia, bipolar disorder and severe recurrent depression.
2 y in genes, is associated with resilience to recurrent depression.
3 ive impairment in older people with previous recurrent depression.
4 hich were observed only in participants with recurrent depression.
5 ortisol awakening response) in patients with recurrent depression.
6 instrumental activities of daily living, and recurrent depression.
7 not observed in children who later developed recurrent depression.
8 ly maintenance psychotherapy did not prevent recurrent depression.
9 fetal risk against the risk of persistent or recurrent depression.
10 quential treatment response among women with recurrent depression.
11 nly tool to prevent relapse in patients with recurrent depression.
12 gitudinal study of offspring of parents with recurrent depression.
13 accompanied by an increased risk of new and recurrent depression.
14 ng stress, in particular in individuals with recurrent depression.
15 otherapy alone for treatment of more severe, recurrent depressions.
16 ficant advantage was observed in more severe recurrent depressions.
17 nalysis of large, rare CNVs in 3106 cases of recurrent depression, 459 controls screened for lifetime
18 Subgroup A; chi(2)=5.34, p=.02), and highly recurrent depression (63.2% of Subgroup B vs 31.8% of Su
19 ntial in euthymic subjects with a history of recurrent depression and 2) the relationship between rec
20 d from a familial collection of early-onset, recurrent depression and were compared with screened con
21 hildren who later developed schizophrenia or recurrent depression as well as in healthy comparison su
22 nus age at onset), course (single episode or recurrent depression), baseline depression severity, tre
23 atment experiences of patients with chronic, recurrent depression being treated by primary care physi
24 ectiveness of this approach in patients with recurrent depression (> or = 3 episodes of depression).
27 e and psychotherapy were less likely to have recurrent depression if they received two years of maint
28 raline is a safe and effective treatment for recurrent depression in patients with recent MI or unsta
30 s therefore do not support the proposal that recurrent depression is associated with long-standing de
32 showed genome-wide significant evidence of a recurrent depression locus in a previous sib-pair study.
33 e life may be part of the AD prodrome, while recurrent depression may be etiologically associated wit
35 atment for relapse prevention for those with recurrent depression, particularly those with more prono
36 2) an affected sibling pair linkage study of recurrent depression (probands from the Depression Netwo
37 ion severity, and melancholic, atypical, and recurrent depression subtypes were all independently ass
38 re collected from 1) a case-control study of recurrent depression (the Depression Case Control [DeCC]
40 ty-three persons aged 60 years or older with recurrent depression were studied: 34 had been depressed
41 istory of PMD should be alert to the risk of recurrent depression when discontinuing hormone therapy.
42 ound that deletion CNVs were associated with recurrent depression, whereas duplications were not.
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