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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
18 a diagnosis of first-episode non-organic or affective psychosis according to ICD-10 criteria, and we
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
24 structural abnormalities to schizophrenia vs affective psychosis, and the possible confounding roles
27 20-25 years), and late-onset (after age 35) affective psychosis at the time of first hospitalization
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
40 rus than did the patients with first-episode affective psychosis or the comparison subjects, with a s
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
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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