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1 ression, and depression (major depression or depressive syndrome).
2 l construct requiring the presence of a full depressive syndrome).
3 en patients (35%) satisfied the criteria for depressive syndrome.
4 fe events were most strongly associated with depressive syndrome.
5 isposed to alcohol dependence (AD) and major depressive syndrome.
6 ndividuals with alcohol dependence and major depressive syndrome.
7 xication and withdrawal effects mistaken for depressive syndromes.
8 se, precipitate or perpetuate some geriatric depressive syndromes.
9 e, precipitate, or perpetuate some geriatric depressive syndromes.
10 wins, we identify and validate a typology of depressive syndromes.
11 k populations, including young patients with depressive syndromes.
12 limbic cortical balance and lead to chronic depressive syndromes.
13 f which 3 represented clinically significant depressive syndromes: (1) mild typical depression, (2) a
15 schizoaffective patients who develop a major depressive syndrome after remission of acute psychosis,
18 ere noted between patients with subthreshold depressive syndromes and those with DSM-IV depressive di
19 elated phenotypes, alcohol dependence, major depressive syndrome, and an endophenotype of electrophys
20 ange of values along three dimensions of the depressive syndrome assessed in the last year (number of
21 individuals met criteria for bipolar I or II depressive syndromes at the time of enrollment and were
22 idepressants were efficacious for women with depressive syndromes during and after menopausal transit
23 ostic categories: major depressive disorder, depressive syndrome, dysthymia, and a comorbid depressio
24 ivity in very young children with a clinical depressive syndrome for which content validity has been
26 indings provide evidence that this preschool depressive syndrome is a robust risk factor for developi
28 pairs concordant for depression had the same depressive syndrome more often than expected by chance a
31 revalence and clinical features of the major depressive syndrome of Alzheimer's disease using data de
33 obands; lack of points of rarity between the depressive syndromes of bipolar II disorder and major de
34 tal pathways in predisposing or perpetuating depressive syndromes or symptoms in elderly patients.
36 toms in mania, rather than the presence of a depressive syndrome per se (i.e., mixed state), that is
37 ia microbiome-brain interactions to mitigate depressive syndromes, providing novel insights into gut