ライフサイエンスコーパス: affective psychosis

1 shared feature across both schizophrenia and affective psychosis.

2 o pathology common to both schizophrenia and affective psychosis.

3 subjects and in patients with first-episode affective psychosis.

4 renia but not in patients with first-episode affective psychosis.

5 enia and also in patients with first-episode affective psychosis.

6 n with schizophrenia and in individuals with affective psychosis.

7 ion compared with controls and patients with 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 lity was lower in those with nonaffective vs affective psychosis.

15 irst-episode psychosis, or affective and non-affective psychosis.

16 iologic contributions to the neurobiology of affective psychosis.

17 alization (13 with schizophrenia and 15 with affective psychosis, 13 of whom had a manic psychosis) a

18 lative to control subjects and patients with affective psychosis (15.4% and 11.0%, respectively), sma

19 ompared with controls (9%) and patients with affective psychosis (7%).

20 a diagnosis of first-episode non-organic or affective psychosis according to ICD-10 criteria, and we

21 l mental illnesses: depression, anxiety, non-affective psychosis, affective psychosis, eating disorde

22 e index children had been diagnosed with non-affective psychosis and 0.5% (N=1,846) with schizophreni

23 a in contrast to patients with first-episode affective psychosis and control subjects.

24 sode schizophrenia relative to first-episode affective psychosis and controls suggests that P300 asym

25 iation between genetic/familial risk for non-affective psychosis and four phenotypes: early age of on

26 chizophrenia, 20 patients with first-episode affective psychosis, and 23 healthy comparison subjects.

27 resenting 443 (49.2%) of 900 people with non-affective psychosis, and 9.1% (5.6-13.3) had current maj

28 n first-episode schizophrenia, first-episode affective psychosis, and control subjects (n = 14 per gr

29 elevated homocysteine levels, patients with affective psychosis, and female patients.

30 to childbirth, focusing on bipolar disorder, affective psychosis, and schizophrenia.

31 structural abnormalities to schizophrenia vs affective psychosis, and the possible confounding roles

32 rus were present in schizophrenia but not in affective psychosis at first hospitalization.

33 volume is present in both schizophrenia and affective psychosis at first hospitalization.

34 20-25 years), and late-onset (after age 35) affective psychosis at the time of first hospitalization

35 sis AUC = 80.5%, 95% CI = 72.1-88.0%, and in affective psychosis AUC = 58.7%, 95% CI = 44.2-72.0%).

36 on (AUC = 75.4%, 95% CI = 67.0-83.3%; in non-affective psychosis AUC = 80.5%, 95% CI = 72.1-88.0%, an

37 agnosed with a primary psychotic disorder or affective psychosis (bipolar disorder with psychosis and

38 In terms of sensitivity, of all non-affective psychosis cases in the index children, 5.2% (N

39 Compared with White members, the risk of affective psychosis diagnosis adjusted for age and sex w

40 have been observed in women with first-onset affective psychosis during the postpartum period.

41 epression, anxiety, non-affective psychosis, affective psychosis, eating disorders, personality disor

42 ith persistent persecutory delusions but non-affective psychosis from two centres: the Oxford Health

43 e patients with schizophrenia and those with affective psychosis had significant left-less-than-right

44 ticipants who were aged 16-35 years, had non-affective psychosis, had been clients of early intervent

45 Outcomes of non-affective psychosis (ICD-10: F20-F29) and schizophrenia

46 ration of psychosis, and lower percentage of affective psychosis in Kancheepuram compared with Ibadan

47 e of mood disorders including depression and affective psychosis, is toxic to specific hippocampal an

48 chizophrenia, 15 patients with first-episode affective psychosis (mainly manic), and 14 healthy compa

49 irst hospitalization), 20 with first-episode affective psychosis (mainly manic), and 24 control subje

50 th healthy controls (P = .006) or those with affective psychosis (mean [SE], 19.34 [0.80]) (P = .03).

51 sode subjects with schizophrenia (n = 15) or affective psychosis (n = 18) or control subjects (n = 18

52 nia (N=17), patients with a first episode of affective psychosis (N=17), and normal comparison subjec

53 %) compared with patients with first-episode affective psychosis or control subjects.

54 us compared with patients with first-episode affective psychosis or healthy comparison subjects.

55 with schizophrenia but not in patients with affective psychosis or in control subjects.

56 round half of the prison population with non-affective psychosis or major depression have a comorbid

57 rus than did the patients with first-episode affective psychosis or the comparison subjects, with a s

58 ns with healthy comparison subjects and with affective psychosis patients.

59 Schizophrenia but not affective psychosis seems to be characterized by a posto

60 Among patients with affective psychosis, there may be heterogeneity of sympt

61 of illness after a first hospitalization for affective psychosis to identify potential outcome predic

62 The absolute risk of non-affective psychosis was 6.4% in those with FHR-P, and 3.

63 Being female and having affective psychosis was associated with improved neuroco

64 he general population (the prevalence of non-affective psychosis was on average 16 times higher, majo

65 rious mental disorder (SMD) (nonaffective or affective psychosis) was found to be positively associat

66 psychiatric hospitalization for treatment of affective psychosis were recruited.

67 People in prison with current non-affective psychosis were significantly more likely to ha

68 ental health services and a diagnosis of non-affective psychosis, which are markers of severity of me

69 ental health services and a diagnosis of non-affective psychosis, which are markers of severity of me

70 d that 3.5% (95% CI 2.2-5.0) had current non-affective psychosis with any comorbid substance use diso

71 Our primary outcomes were comorbid non-affective psychosis with substance use disorders and com