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1 o pathology common to both schizophrenia and affective psychosis.
2  subjects and in patients with first-episode affective psychosis.
3 renia but not in patients with first-episode affective psychosis.
4 enia and also in patients with first-episode affective psychosis.
5 n with schizophrenia and in individuals with affective psychosis.
6 ion compared with controls and patients with affective psychosis.
7 iologic contributions to the neurobiology of affective psychosis.
8 icit is present in schizophrenia, but not in affective psychosis.
9 not present at the first hospitalization for affective psychosis.
10 renia but not in patients with first-episode affective psychosis.
11 on and is different from the presentation of affective psychosis.
12 olume decreases are present in patients with affective psychosis.
13 he year after a first hospitalization for an affective psychosis.
14 shared feature across both schizophrenia and affective psychosis.
15 alization (13 with schizophrenia and 15 with affective psychosis, 13 of whom had a manic psychosis) a
16 lative to control subjects and patients with affective psychosis (15.4% and 11.0%, respectively), sma
17 ompared with controls (9%) and patients with affective psychosis (7%).
18  a diagnosis of first-episode non-organic or affective psychosis according to ICD-10 criteria, and we
19 a in contrast to patients with first-episode affective psychosis and control subjects.
20 sode schizophrenia relative to first-episode affective psychosis and controls suggests that P300 asym
21 chizophrenia, 20 patients with first-episode affective psychosis, and 23 healthy comparison subjects.
22 n first-episode schizophrenia, first-episode affective psychosis, and control subjects (n = 14 per gr
23 to childbirth, focusing on bipolar disorder, affective psychosis, and schizophrenia.
24 structural abnormalities to schizophrenia vs affective psychosis, and the possible confounding roles
25 rus were present in schizophrenia but not in affective psychosis at first hospitalization.
26  volume is present in both schizophrenia and affective psychosis at first hospitalization.
27  20-25 years), and late-onset (after age 35) affective psychosis at the time of first hospitalization
28 have been observed in women with first-onset affective psychosis during the postpartum period.
29 ith persistent persecutory delusions but non-affective psychosis from two centres: the Oxford Health
30 e patients with schizophrenia and those with affective psychosis had significant left-less-than-right
31 ticipants who were aged 16-35 years, had non-affective psychosis, had been clients of early intervent
32 e of mood disorders including depression and affective psychosis, is toxic to specific hippocampal an
33 chizophrenia, 15 patients with first-episode affective psychosis (mainly manic), and 14 healthy compa
34 irst hospitalization), 20 with first-episode affective psychosis (mainly manic), and 24 control subje
35 sode subjects with schizophrenia (n = 15) or affective psychosis (n = 18) or control subjects (n = 18
36 nia (N=17), patients with a first episode of affective psychosis (N=17), and normal comparison subjec
37 %) compared with patients with first-episode affective psychosis or control subjects.
38 us compared with patients with first-episode affective psychosis or healthy comparison subjects.
39  with schizophrenia but not in patients with affective psychosis or in control subjects.
40 rus than did the patients with first-episode affective psychosis or the comparison subjects, with a s
41 ns with healthy comparison subjects and with affective psychosis patients.
42                        Schizophrenia but not affective psychosis seems to be characterized by a posto
43                          Among patients with affective psychosis, there may be heterogeneity of sympt
44 of illness after a first hospitalization for affective psychosis to identify potential outcome predic
45 rious mental disorder (SMD) (nonaffective or affective psychosis) was found to be positively associat
46 psychiatric hospitalization for treatment of affective psychosis were recruited.
47 ental health services and a diagnosis of non-affective psychosis, which are markers of severity of me
48 ental health services and a diagnosis of non-affective psychosis, which are markers of severity of me

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