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1 q11DS, 55 (13.4%) were diagnosed as having a psychotic disorder.
2 ith later hospitalization for a nonaffective psychotic disorder.
3 unded yet tenacious beliefs and a symptom of psychotic disorder.
4 spectively identify patients at high risk of psychotic disorder.
5 se who do and do not convert to a full-blown psychotic disorder.
6 Schizophrenia is currently classified as a psychotic disorder.
7 participants were known to have developed a psychotic disorder.
8 ted with a later diagnosis of a nonaffective psychotic disorder.
9 with at least two siblings suffering from a psychotic disorder.
10 Schizophrenia is a highly heritable psychotic disorder.
11 the criteria for schizophrenia or a related psychotic disorder.
12 es not reflect the presence of an underlying psychotic disorder.
13 cting later hospitalization for nonaffective psychotic disorder.
14 lly defined suspected PEs, definite PEs, and psychotic disorder.
15 subjects clinically at risk of developing a psychotic disorder.
16 escence is associated with increased risk of psychotic disorders.
17 ls of neural noise have been demonstrated in psychotic disorders.
18 number of autoimmune diseases in people with psychotic disorders.
19 etting the stage for vulnerability for later psychotic disorders.
20 ajor psychiatric disorders, particularly for psychotic disorders.
21 tions in the hippocampus were evident across psychotic disorders.
22 e underlying mechanism and for prevention of psychotic disorders.
23 help elucidate etiological underpinnings of psychotic disorders.
24 but remain less well characterized in other psychotic disorders.
25 ith the lack of friendships in patients with psychotic disorders.
26 pression, posttraumatic stress disorder, and psychotic disorders.
27 ball responses among patients with different psychotic disorders.
28 ciated with increased risk for affective and psychotic disorders.
29 ture of schizophrenia and is common in other psychotic disorders.
30 ed to be a pathophysiological contributor to psychotic disorders.
31 ctive study of first-admission patients with psychotic disorders.
32 ed dopamine synthesis capacity to particular psychotic disorders.
33 misdiagnosed in the United States as primary psychotic disorders.
34 delusions are a common symptom of a range of psychotic disorders.
35 es predisposing to schizophrenia and related psychotic disorders.
36 tially targeted by schizophrenia and related psychotic disorders.
37 mprove functional outcome among persons with psychotic disorders.
38 Among the men, 2.2% were hospitalized with psychotic disorders.
39 brain structural abnormality common to both psychotic disorders.
40 from that of patients with nonschizophrenic psychotic disorders.
41 ate may play a role in neurodegenerative and psychotic disorders.
42 ion in first-episode schizophrenia and other psychotic disorders.
43 represents a novel treatment development for psychotic disorders.
44 tical connectivity that putatively underlies psychotic disorders.
45 90s but persisted for African Americans with psychotic disorders.
46 and Related Health Problems, Tenth Revision psychotic disorders.
47 y living situation of older outpatients with psychotic disorders.
48 age-specific fertility rates for women with psychotic disorders.
49 al of maintenance treatment in patients with psychotic disorders.
50 women of childbearing age (15-44 years) with psychotic disorders.
51 l exposures might increase the later risk of psychotic disorders.
52 atients (ages 18 to 55 years) with DSM-III-R psychotic disorders.
53 treatment, particularly for individuals with psychotic disorders.
54 treated a higher proportion of patients with psychotic disorders.
55 e that included the full range of functional psychotic disorders.
56 ve sample of persons newly hospitalized with psychotic disorders.
57 ers, then those with schizophrenia and other psychotic disorders.
58 than half of that for patients with mood or psychotic disorders.
59 tion among young adults with newly diagnosed psychotic disorders.
60 ant effect on the etiology and the course of psychotic disorders.
61 hat may contribute to the pathophysiology of psychotic disorders.
62 eptor hypofunction in the pathophysiology of psychotic disorders.
63 mechanism underlies cognitive impairment in psychotic disorders.
64 tervention and the personalized treatment of psychotic disorders.
65 ted to the underlying familial diathesis for psychotic disorders.
66 le evidence that the thalamus is abnormal in psychotic disorders.
67 l categorization schemes for differentiating psychotic disorders.
68 al characteristic of schizophrenia and other psychotic disorders.
69 e that cannabis use can increase the risk of psychotic disorders.
70 nditions: post-traumatic stress disorder and psychotic disorders.
71 escence, is important in the pathogenesis of psychotic disorders.
72 ssessment and management in individuals with psychotic disorders.
73 on to baseline cannabis use and diagnosis of psychotic disorders.
74 e have increased prevalence in patients with psychotic disorders.
75 ce of persecutory delusions in patients with psychotic disorders.
76 psychophysiological alterations observed in psychotic disorders.
77 ups of disorders, the neurodevelopmental and psychotic disorders.
78 se, and type of cannabis used on the risk of psychotic disorders.
79 ffected the association between cannabis and psychotic disorders.
80 tanding of common mechanisms between FTD and psychotic disorders.
81 e of 5-HT2B receptors in the neurobiology of psychotic disorders.
82 e pathophysiology of schizophrenia and other psychotic disorders.
83 malities reported in adults with established psychotic disorders.
86 as mood disorders, followed by schizophrenia/psychotic disorders (14.6%), anxiety disorders (9.3%), a
87 is study of 304 adults at ultrahigh risk for psychotic disorders, 153 (50.3%) received omega-3 PUFAs
88 continuum model of cognitive dysfunction in psychotic disorders, 3) reports familiality of cognitive
89 with first-episode schizophrenia and related psychotic disorders, 34 patients with first-episode nons
90 ssment was lower in patients who developed a psychotic disorder (65.5 [12.0]) compared with those wit
93 ct, a study of first-admission patients with psychotic disorders admitted to psychiatric facilities b
94 n, and deprivation on risk of developing any psychotic disorder, all with qualitative patterns of int
95 en thought to be critical in the etiology of psychotic disorders, although the differential roles pla
96 dysfunction has often been reported in other psychotic disorders, although there are inconsistencies
97 y marker in assessing the risk of developing psychotic disorders among ultra-high-risk individuals.
98 ease in the risk of having a broadly defined psychotic disorder, an almost 8.5-fold increase in the r
99 Most were African American and had a chronic psychotic disorder and a comorbid substance use disorder
100 ical psychotic symptoms), 50 patients with a psychotic disorder and auditory verbal hallucinations, a
103 pocampal hypermetabolism leads to atrophy in psychotic disorder and suggest glutamate as a pathogenic
104 s between those who subsequently developed a psychotic disorder and those who did not was distinguish
105 ifty outpatients with schizophrenia or other psychotic disorders and 19 normal comparison subjects ag
106 e role of oxytocin in the pathophysiology of psychotic disorders and addictions and to extend clinica
110 plications for understanding the etiology of psychotic disorders and for informing social policy.
112 ing study in a large series of probands with psychotic disorders and healthy volunteers as part of th
113 Implications for treatment of parents with psychotic disorders and high-risk children are discussed
114 are utilized extensively in the treatment of psychotic disorders and other psychiatric conditions, bu
115 cal displacement of the postcentral gyrus in psychotic disorders and support the hypothesis that anom
116 s mortality; 2) mortality among persons with psychotic disorders and the extent to which cannabis use
117 ations for understanding the pathogenesis of psychotic disorders and the specific deficits that seem
119 road array of intermediate phenotypes across psychotic disorders and to test the hypothesis that inte
121 organic mental disorders, mood disorders, or psychotic disorders and who were discharged after a comp
123 , delusional disorder, or affective-spectrum psychotic disorder, and psychotic symptoms scoring at le
124 ith schizophrenia, 45 individuals with other psychotic disorders, and 33 healthy control subjects.
125 familiality of cognitive impairments across psychotic disorders, and 4) evaluates cognitive impairme
126 ble death, especially among individuals with psychotic disorders, and may also be common among noncli
129 mic-pituitary-adrenal activity indicate that psychotic disorders are associated with elevated cortiso
132 al manifestations of schizophrenia and other psychotic disorders are correlated in affected sibling p
138 nding the basis for deficient PPI and MMN in psychotic disorders, as reduced NMDA activity is implica
139 nd is thought to be dysregulated in mood and psychotic disorders, as well as in various phases of opi
142 092 individuals (0.95%) not diagnosed with a psychotic disorder at the time of examination were hospi
143 requency of experiences at age 12 predicting psychotic disorders at age 18 ranged from 5.5% to 22.8%.
145 experiences (PE; n=20) at increased risk for psychotic disorders; (b) people with extremely elevated
146 as not associated with an excess of familial psychotic disorder but was associated with a higher morb
147 equently seen in patients with first-episode psychotic disorders but are generally considered to be d
148 ourse, cognitive deficits are present in all psychotic disorders but are most severe and pervasive in
149 At the time of investigation, none had any psychotic disorder, but on detailed interview some of th
150 nt dopamine antagonist that is used to treat psychotic disorders, but 50% of treated patients develop
151 etic contribution to the major categories of psychotic disorders, but few of these have employed oper
152 s of violence are increased in patients with psychotic disorders, but the contribution of triggers fo
153 ound an excess mortality among subjects with psychotic disorders, but the level did not differ betwee
154 pothesis that cannabis increases the risk of psychotic disorders by inducing the same dopaminergic al
155 le participants were patients with diagnosed psychotic disorders (clinical group) and adults in the g
158 abis every day conferred the highest risk of psychotic disorders compared with no use of cannabis (ad
159 with a doubling of the risk of developing a psychotic disorder, compared with no relevant complicati
163 1957 in Finland were screened for nonorganic psychotic disorder diagnoses as recorded on an inpatient
164 ata for age, sex, ethnicity, marital status, psychotic disorder diagnosis, subsequent hospital admiss
169 efficiency was also significantly reduced in psychotic disorders (F3,587 = 4.01, P = .008) and positi
170 in an epidemiologically defined cohort with psychotic disorders followed for 20 years after first ho
174 y control participants and 375 patients with psychotic disorders from the Bipolar-Schizophrenia Netwo
175 anomalous cerebral asymmetry is a feature of psychotic disorders generally, including psychotic mood
177 disorders and patients with nonschizophrenic psychotic disorders had smaller left entorhinal cortex v
178 sorders, schizophrenia, and nonschizophrenic psychotic disorders) had substantially increased risks o
179 elevated dopamine synthesis capacity once a psychotic disorder has developed, little is known about
180 tent methamphetamine psychosis and a primary psychotic disorder has grown increasingly important.
184 general population, individuals with severe psychotic disorders have increased risks for smoking (od
185 ng-term trajectories of social impairment in psychotic disorders have rarely been studied systematica
188 the development of psychotic experiences and psychotic disorders in a large population-based sample o
189 e calculated an overall relative risk of new psychotic disorders in daily smokers versus non-smokers
191 symptoms of patients later hospitalized for psychotic disorders in primary mental health outpatient
192 comorbidity between substance use and severe psychotic disorders in the Genomic Psychiatry Cohort.
196 Diabetes is highly prevalent in people with psychotic disorders, including schizophrenia and schizoa
201 duals who may develop schizophrenia or other psychotic disorders is critical for predicting psychosis
202 etes pharmacotherapy and drug management for psychotic disorders is essential, irrespective of whethe
203 Knowledge of fertility rates in women with psychotic disorders is fundamental for clinicians and re
205 he general cognitive deficit observed across psychotic disorders is similarly associated with functio
206 th concern associated with schizophrenia and psychotic disorders is the long-term disability that inv
207 ffective acute treatment for severe mood and psychotic disorders, it remains controversial because of
208 resent with unusual symptoms associated with psychotic disorders, leading to misdiagnosis and inappro
209 prevent the onset of schizophrenia and other psychotic disorders, longitudinal high-risk research on
210 t histories of major depression, anxiety, or psychotic disorders (low-risk group) completed a functio
211 psychiatric disorders and that patients with psychotic disorders may develop dementia more often than
212 and psychotic depression suggest that these psychotic disorders may have common pathophysiological f
213 elevating dopamine antagonists used to treat psychotic disorders may initiate and promote breast canc
214 x volume in first-episode, neuroleptic-naive psychotic disorders may not be a confound of the effects
215 t is unique to schizophrenia or is common to psychotic disorders more broadly, and its associations w
217 N=37), depressive psychosis (N=39), or other psychotic disorders (N=46) following index presentation,
219 (ASD) are at increased risk for nonaffective psychotic disorder (NAPD) or bipolar disorder (BD) is un
220 of neighbourhood variations of non-affective psychotic disorders (NAPD) have focused mainly on incide
222 abnormalities were seen in the subjects with psychotic disorder not otherwise specified except that t
223 izophrenia, of children and adolescents with psychotic disorder not otherwise specified to that of ch
224 th childhood-onset schizophrenia and 26 with psychotic disorder not otherwise specified) and their re
227 eater than twofold increased likelihood of a psychotic disorder (odds ratio = 2.18 [95% confidence in
228 ntly increased risk for the development of a psychotic disorder (odds ratio = 2.49; 95% CI, 1.24-5.00
233 ued because of an adverse event (four due to psychotic disorder or hallucination within 10 days of st
234 erlie the propensity of stress to exacerbate psychotic disorders or predispose an individual to drug-
236 upport an overall change in the incidence of psychotic disorder over time, though diagnostic shifts (
238 eir patients with schizophrenia or a related psychotic disorder participated in a European multi-cent
240 igh across a broad spectrum of patients with psychotic disorders; patients with a history of a curren
242 e compared between 243 control subjects, 388 psychotic disorder probands, and 300 of their first-degr
243 Of the remaining patients, nine developed a psychotic disorder (psychotic transition group) and 15 d
245 en reported in a proportion of patients with psychotic disorders, raising hopes for more appropriate
247 effective for individuals with nonaffective psychotic disorders, reducing hospital readmissions appr
249 utoantibodies against glutamatergic NMDAR in psychotic disorders remains controversial, with detectio
252 sive-compulsive and panic symptoms and three psychotic disorders--schizophrenia/schizoaffective disor
253 ring a medical visit, patients completed the psychotic disorders section of the Mini International Ne
254 cts of organic-induced and substance-induced psychotic disorder show that our diagnostic classificati
256 asingly used in the treatment of a number of psychotic disorders since their introduction in 1988, wi
257 gnificantly mediated the association between psychotic disorder status and general cognition (beta =
259 ences differed from that seen in adults with psychotic disorders, suggesting important differences be
260 markedly lower fertility rates in women with psychotic disorders than in matched normal comparison su
261 a substance-induced psychosis and a primary psychotic disorder that co-occurs with the use of alcoho
262 to dissecting the genetic basis of mood and psychotic disorders that can inform future large-scale c
263 clinicians to correctly classify early-phase psychotic disorders that co-occur with substance use.
264 immune response in schizophrenia and related psychotic disorders that, we think, will be of interest
265 en neuronal ensembles has been implicated in psychotic disorders, the neuronal activity of N-desmethy
266 previous diagnosis of schizophrenia or other psychotic disorder, those with glomerular disease, tubul
267 ioning, but few studies have linked risk for psychotic disorders to a neural measure evoked during a
268 ng clinical utility of antipsychotics beyond psychotic disorders to include depressive, bipolar, and
269 amination were hospitalized for nonaffective psychotic disorder up to 9 years after the index examina
270 D IMPLICATIONS OF KEY FINDINGS: Incidence of psychotic disorders varied markedly by age, sex, place a
272 or bipolar disorder, schizophrenia, or other psychotic disorder was recorded on at least one inpatien
273 Severity of cognitive impairments across psychotic disorders was consistent with a continuum mode
274 cortex volume of patients with nondelusional psychotic disorders was significantly smaller than that
275 cohort of 470 first-admission patients with psychotic disorders was systematically assessed at basel
276 replication; psychotic experiences (PEs) and psychotic disorder were measured by a semistructured int
277 le-aged and elderly outpatients with primary psychotic disorders were administered the UPSA, the Matt
280 hirty-two hospitalized patients with chronic psychotic disorders were randomly assigned to community
282 2, positive predictive values for predicting psychotic disorders were too low to offer real potential
283 represent candidates that may be causal for psychotic disorders when considered in the context of th
284 tern of cortical thinning as patients with a psychotic disorder, which is suggestive of a similar, bu
285 n a generalizability cohort of patients with psychotic disorders who were hospitalized for an acute p
286 ded a sample of patients with a pre-existing psychotic disorder with a follow-up duration of at least
287 ssion to compare persons hospitalized with a psychotic disorder with those who had never been hospita
290 Fifteen individuals with VCFS (30%) had a psychotic disorder, with 24% (n = 12) fulfilling DSM-IV
291 s not associated with an increased risk of a psychotic disorder, with lifetime cannabis use, or with
292 The UHR patients are at long-term risk for psychotic disorder, with the highest risk in the first 2
293 the hippocampal subfields were seen in all 3 psychotic disorders, with the most prominent differences
294 ed risk for hospitalization for nonaffective psychotic disorder within 14 days after examination (haz
296 ed on current clinical criteria convert to a psychotic disorder within a 2.5-year follow-up period.
297 en who had never been hospitalized, men with psychotic disorders without a personality disorder or a
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