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1 hippocampal activity that is correlated with positive symptoms.
2 spindles correlated with greater severity of positive symptoms.
3 l striatum was correlated with the degree of positive symptoms.
4 induced cognitive deficits and negative and positive symptoms.
5 e-induced cognitive deficits or negative and positive symptoms.
6 lusion correlated with increased severity of positive symptoms.
7 e changes were associated with the degree of positive symptoms.
8 d cingulate gyri correlated with severity of positive symptoms.
9 in negative and depressive symptoms but not positive symptoms.
10 The majority targeted treatment resistant positive symptoms.
11 ning as well as decreases in the severity of positive symptoms.
12 variability in symptom severity or negative/positive symptoms.
13 nse criteria required sustained remission of positive symptoms.
14 no difference between groups in the rate of positive symptoms.
15 impairment) and in those with predominantly positive symptoms.
16 ative symptoms from those with predominantly positive symptoms.
17 ognitive disorganization but not negative or positive symptoms.
18 detect potential correlations between FD and positive symptoms.
19 y of life, symptom severity, or remission of positive symptoms.
20 , symptom severity, and time to remission of positive symptoms.
21 apine without glycine had a 35% reduction in positive symptoms.
22 ributable to the Scale for the Assessment of Positive Symptoms.
23 ymptoms and temporal lobe abnormalities with positive symptoms.
24 ted with transient emergence or worsening of positive symptoms.
25 relevant in the initial development phase of positive symptoms.
26 chronic hospital patients did not differ on positive symptoms.
27 pine was superior to haloperidol in treating positive symptoms.
28 the putamen were associated with more severe positive symptoms.
29 ) than in normal subjects and are related to positive symptoms.
30 d with greater severity of both negative and positive symptoms.
31 pontaneous SCR frequency was associated with positive symptoms.
32 Symptoms and the Scale for the Assessment of Positive Symptoms.
33 showing quetiapine's consistency in reducing positive symptoms.
34 s memory responses were positively linked to positive symptoms.
35 ive rehabilitation, and coping with residual positive symptoms.
36 ng Scale, and the Scale of the Assessment of Positive Symptoms.
37 This deficit correlated with positive symptoms.
38 iated with higher suspiciousness and overall positive symptoms.
39 d antipsychotic drugs only address primarily positive symptoms.
40 impairment, antipsychotic treatment or even positive symptoms.
41 sm was significantly correlated with SCZ and positive symptoms.
42 (BPRS) were used to quantify the severity of positive symptoms.
43 ed response in patients who only experienced positive symptoms.
44 putamen correlated with less improvement in positive symptoms.
45 ed with opposite correlations between RD and positive symptoms.
46 The alpha activity correlated with positive symptoms.
47 e to PFC-dependent correlates of negative or positive symptoms.
48 ot induce clinically significant increase in positive symptoms.
49 ith age, and NAAc correlated negatively with positive symptoms.
50 ences compared with placebo for reduction of positive symptoms (31 179 participants) varied from -0.6
51 d patients showed significant improvement in positive symptoms (52% and 44% reductions from baseline,
52 re as follows: amisulpride for patients with positive symptoms, 537 mg/day and 85.8 mg; aripiprazole,
53 t of which have been shown to correlate with positive symptoms: aberrant learning for neutral cues (a
54 th schizophrenia in symptomatic remission of positive symptoms according to Andreasen, and 24 healthy
55 rome to determine which patients receive the positive symptom advantage of clozapine and the extent o
58 of medication nonadherence on the return of positive symptoms among recent-onset schizophrenia patie
59 CGI severity and improvement ratings, PANSS positive symptom and general psychopathology subscales,
62 tive and Negative Syndrome Scale factors for positive symptoms and anxiety/depression were greater wi
66 efits of the program included a reduction in positive symptoms and in symptom exacerbations and an in
67 e negatively correlated with the severity of positive symptoms and medication dose in SZ patients.
69 Clozapine was superior to risperidone for positive symptoms and parkinsonian side effects, but the
70 s and failure to respond, as well as between positive symptoms and production of erroneous responses.
71 ous phasic dopamine release helps to explain positive symptoms and provides a unified explanation for
72 l manifestation, prevents the development of positive symptoms and related neurobiological alteration
73 ting scales (the Scale for the Assessment of Positive Symptoms and the alogia subscale of the Scale f
74 onal outcomes were not entirely dependent on positive symptoms and the development of psychosis, furt
75 a symptoms-and-function definition based on positive symptoms and the modified Global Assessment of
77 ssessed with the Scale for the Assessment of Positive Symptoms and the Scale for the Assessment of Ne
78 ere rated on the Scale for the Assessment of Positive Symptoms and the Scale for the Assessment of Ne
79 ssessed with the Scale for the Assessment of Positive Symptoms and the Scale for the Assessment of Ne
80 al scores on the Scale for the Assessment of Positive Symptoms and the Scale for the Assessment of Ne
81 ssessed with the Scale for the Assessment of Positive Symptoms and the Scale for the Assessment of Ne
82 ia significantly correlated with severity of positive symptoms and thought disorder and with impairme
83 son subjects were evaluated for negative and positive symptoms and underwent comprehensive neuropsych
84 es >=3 using the Scale for the Assessment of Positive Symptoms) and associated psychotic and nonpsych
85 namely enhanced MK-801 psychomotor response (positive symptoms) and decreased working memory (cogniti
86 Three symptom factors-negative symptoms, positive symptoms, and affective symptoms-were all signi
87 the medial temporal lobe was correlated with positive symptoms, and baseline [(11)C]flumazenil VT in
89 nsolidation in schizophrenia, contributes to positive symptoms, and is a promising novel target for t
90 ing predominance of women, lower severity of positive symptoms, and lower average antipsychotic dose
91 able schizophrenia, predominant NSS, limited positive symptoms, and maintained on stable atypical ant
92 the ES group was negatively correlated with positive symptoms, and positively correlated with negati
95 Nursing home patients had the least severe positive symptoms, and the acutely ill and chronic hospi
97 chizophrenia during symptomatic remission of positive symptoms, and whether potential alterations rel
98 represented dimensions of mania, depression, positive symptoms, anxiety, negative symptoms and disorg
99 (n = 17, 8.5%), which was unrelated to SIPS-positive symptoms, any DSM diagnosis or other clinical c
100 e rehabilitation and training in coping with positive symptoms appear to be promising interventions,
102 d in the illness, correlate with measures of positive symptoms, are consistent with models of disease
105 gh preceded by reflux (mainly distal), 56% a positive symptom association probability (SAP(C-R (2 min
106 ted temporal associations, with 48% having a positive symptom association probability (SAP(R-C)) for
107 Symptoms and the Scale for the Assessment of Positive Symptoms at 18 months after randomization.
108 greater improvement than control subjects on positive symptoms at all time points and on negative sym
110 nly if they exhibited one or more attenuated positive symptoms at moderate to severe, but not psychot
111 Symptoms and the Scale for the Assessment of Positive Symptoms) at index hospitalization and quality
112 P group, only the ADS SA was associated with positive symptoms (beta = -0.08; 95% CI, -0.13 to -0.02;
113 ationship between longer DUP and more severe positive symptoms (beta=-0.16, p=4.5x10(-8) ), more seve
114 prediction model was developed and included positive symptoms, bizarre thinking, sleep disturbances,
115 hrenia, especially those that treat not only positive symptoms but also the negative and cognitive sy
116 therapy, clozapine has superior efficacy for positive symptoms but not negative symptoms and is assoc
117 depressive symptoms correlated with that of positive symptoms but not with age, gender, negative sym
118 oduce fairly robust clinical benefit against positive symptoms but typically have minimal therapeutic
119 ntipsychotic drugs (APDs) show efficacy with positive symptoms, but are limited in treating negative
120 ative symptoms at any time after control for positive symptoms, but its effects on positive symptoms
121 of haloperidol over olanzapine for improving positive symptoms, but the benefit was scale-dependent:
122 iated with the transient amphetamine-induced positive-symptom change, as observed in schizophrenia.
123 results suggest that the neural substrate of positive symptoms changes with illness chronicity, and t
124 bles, with end point differences in the BPRS positive-symptom cluster score showing quetiapine's cons
125 condary efficacy variables included the BPRS positive-symptom cluster score, the Modified Scale for t
126 Severity of Illness item; and P = .003, BPRS positive-symptom cluster) differences were identified be
127 , despite an absence of depressive symptoms, positive symptoms, comorbid systemic illnesses, or medic
128 ssions' Severity of Illness Scale as well as positive symptoms compared with those receiving placebo.
129 significantly with risperidone response were positive symptoms, conceptual disorganization, akathisia
130 he diagnosis of FAPS is made on the basis of positive symptom criteria and a longstanding history of
131 ore homogeneous high-risk sample (attenuated positive symptom criteria only, age range of mid-teens t
132 elapse (dCC-NC=0.36 vs dDC-NC=0.02, p=0.04), positive symptoms (dCC-NC=0.15 vs dDC-NC=-0.30, p=0.05)
134 r schizophrenia with suboptimally controlled positive symptoms despite treatment with antipsychotics.
135 , with the strongest effect observed for the positive symptom dimension, which includes suspiciousnes
136 Symptoms and the Scale for the Assessment of Positive Symptoms divided into 3 domains: psychotic, neg
137 as associated with treatment response in the positive symptom domain in both clinical cohorts (p valu
138 st that patients with minimal improvement in positive symptoms during the first week of treatment wit
140 personality disorder [healthy aging], mania/positive symptoms [early psychosis]), impaired thought p
141 ate connectivity pattern and the severity of positive symptoms evaluated with the Positive and Negati
142 t (i.e., mediated by differential effects on positive symptoms, extrapyramidal symptoms, or mood).
144 s the mean change from baseline in the PANSS Positive Symptom Factor Score (PSFS) at week 12, analyse
146 hed expression and disordered relating), two positive symptom factors (bizarre delusions and auditory
147 (two consecutive ratings without significant positive symptoms) for rare allele carriers versus wild
148 (1) a symptoms-only definition based on the positive symptoms from the Scale of Prodromal Symptoms a
149 idate prognostic factors: negative symptoms, positive symptoms, functioning, depressive symptoms, sui
150 he studies examined, MCT was associated with positive symptoms (g = 0.50; 95% CI, 0.34-0.67), delusio
153 rs1036145 showed significant improvement in positive symptoms, general psychopathology, and thought
154 ither SNP, showed significant improvement in positive symptoms, general psychopathology, thought dist
155 g positive outcomes for both functioning and positive symptoms; group 2 (49%) exhibited moderate impa
157 ively; P = .01; between-group d = -0.66) and positive symptoms (hallucinations, delusions, disorganiz
158 th schizophrenia in symptomatic remission of positive symptoms have decreased striatal dopamine synth
159 onse, less relapse); for schizophrenia, less positive symptoms/higher depressive symptoms (remission,
160 minergic function, are effective at reducing positive symptoms (i.e. delusions and hallucinations), t
161 ring treatment, the mean score for prodromal positive symptoms improved more in the olanzapine group
164 hermore, clozapine was superior in improving positive symptoms in both study groups, but not for nega
165 ments in functional outcome, motivation, and positive symptoms in low-functioning patients with signi
166 study examined the frequency of negative and positive symptoms in nonpsychotic patients with temporal
170 is effective in treating negative as well as positive symptoms in schizophrenia resistant to standard
172 toms of schizophrenia are only effective for positive symptoms in some individuals, and have consider
174 ut statistically significant, improvement in positive symptoms in the active rTMS group (p = .047, ef
175 y in schizophrenia predicted the severity of positive symptoms in the disorder, such as hallucination
177 well as between negative and positive (PANSS-Positive) symptoms in influencing functional outcome of
179 n, that aberrant salience (and the resulting positive symptoms) in schizophrenia may arise, at least
180 thological features manifest behaviorally as positive symptoms (including hallucinations, delusions a
181 he flawed agency judgments characteristic of positive symptoms, including auditory hallucinations and
182 dopamine receptor antagonism in ameliorating positive symptoms, including auditory hallucinations, in
183 ried forward analyses on the sum of selected positive symptom items of the Brief Psychiatric Rating S
185 chizophrenia patients with both negative and positive symptoms (n = 11) and schizophrenia patients wi
187 rom confirmatory factor analysis relating to positive symptoms, negative symptoms of diminished expre
188 tures that can be parsed into three domains: positive symptoms, negative symptoms, and cognitive defi
189 ss a complex symptomatology characterized by positive symptoms, negative symptoms, and cognitive impa
190 ng of the boundaries and connections between positive symptoms, negative symptoms, and role functioni
191 onal solution separated individuals based on positive symptoms, negative symptoms, depression, and fu
192 S share fundamental clinical features (i.e., positive symptoms, negative symptoms, functional deficit
193 groups that separated on primary deficits of positive symptoms, negative symptoms, global functioning
194 the presence of 3 clusters corresponding to positive symptoms; negative symptoms and work functionin
195 ntipsychotic medication in the management of positive symptoms of acute schizophrenia as well as nega
197 ospitalisation and perceived risk to others, positive symptoms of psychosis, reduced insight into ill
201 nt in social and communication function, and positive symptoms of restricted and repetitive behaviors
202 nt in all medications that effectively treat positive symptoms of schizophrenia (e.g., delusions and
204 nistered Dissociative States Scale (P<.001); positive symptoms of schizophrenia as assessed by the Br
205 ic drugs are widely thought to alleviate the positive symptoms of schizophrenia by antagonizing dopam
207 When SAR218645 was tested in models of the positive symptoms of schizophrenia, it reduced head twit
208 f the former appears to track improvement of positive symptoms of schizophrenia, the latter have rece
213 with predominantly negative or predominantly positive symptoms on the basis of their post-drug-washou
215 ed with an increase in the severity of total positive symptoms over time (r=-0.33; df=47; P=0.02), mo
216 in and between group reductions in both BPRS positive symptoms (p = 0.02, d = -0.36; p = 0.008, d = -
217 han in HS (p<0.032), and was associated with positive symptoms (p<0.007), antipsychotic load (p<0.015
218 ody of evidence demonstrates that persistent positive symptoms, particularly delusions, can be improv
219 normalities than subjects with predominantly positive symptoms, particularly in frontal, temporal, an
220 sessed once per test day, while negative and positive symptoms, perceptual alterations, and a number
221 ol for positive symptoms, but its effects on positive symptoms persisted after control for negative s
222 roup was indirect (ie, partially mediated by positive symptoms) (probit coefficient [beta] = 0.12; P
224 enrolled 75 CHR individuals with attenuated positive symptom psychosis-risk syndrome as defined by t
225 a separate sibpair analysis using scores on positive-symptom (psychotic), negative-symptom (deficit)
226 ions in K(i) correlated with improvements in positive symptoms (r = 0.5, p < 0.05), but not with chan
227 cantly associated with increased severity of positive symptoms (r=0.19; q=0.05) in the psychosis spec
228 dered thought patterns associated with fewer positive symptoms rather than cognitive deficits in the
230 cipants met criteria for conversion if their positive symptoms reached the fully psychotic range and
234 on's disease-adapted scale for assessment of positive symptoms (SAPS-PD) in all patients who received
235 on Rating Scale, Scale for the Assessment of Positive Symptoms, Scale for the Assessment of Negative
236 e ratings of the Scale for the Assessment of Positive Symptoms, Scale for the Assessment of Negative
238 ief Psychiatric Rating Scale total score and positive symptom score, Scale for the Assessment of Nega
239 ically significant treatment effect on PANSS positive symptom scores (beta for change in raloxifene v
240 nsion were related to greater BPRS total and positive symptom scores and longer time hospitalized.
241 nction signal was positively correlated with positive symptom scores during deceptive repayments.
243 any CSF alteration had significantly higher positive symptom scores than those without alterations (
245 The response in the amygdala correlated with positive symptom severity (r = .16, P = .01) but not wit
246 was mainly restricted to the subcortex, with positive symptom severity being associated with midbrain
249 individuals in early psychosis stages beyond positive symptom severity to investigate specificity rel
254 ity was associated with greater negative and positive symptom severity; a pattern that was also evide
255 in early psychosis and could be involved in positive symptoms severity in males, indicating potentia
258 mptoms (primary outcomes), overall symptoms, positive symptoms, side effects, exacerbation of psychos
261 n difference: -0.24, 95% CI=-0.39 to -0.09), positive symptoms (standardized mean difference: -0.17,
262 augmented AMPH-induced peak changes in PANSS positive symptom subscale and both subjective and object
263 e to week 6 and week 12, mean BPRS total and positive symptom subscale scores were reduced significan
264 sessed by the Brief Psychiatric Rating Scale positive symptoms subscale (P<.001); negative symptoms a
265 dary end points were the change in the PANSS positive symptom subscore, the score on the Clinical Glo
266 not be a sufficient mechanism for explaining positive symptoms such as auditory hallucinations in sch
268 aracteristic of schizophrenia and related to positive symptoms, such as auditory hallucinations.
269 proteins with 6-month follow-up measures of positive symptoms summary (PSS) scores and functional ou
271 ess onset (t = -1.355, df = 277, P = 0.177), positive symptoms (t = 0.249, df = 289, P = 0.803), nega
272 longer hospital admissions, and more severe positive symptoms than for individuals who discontinue c
273 ption betel chewers had significantly milder positive symptoms than low-consumption chewers over 1 ye
274 ide stratifications beyond the expression of positive symptoms that cut across illness stages and dia
275 res included the Scale for the Assessment of Positive Symptoms, the Scale for the Assessment of Negat
276 antipsychotic efficacy and rodent models of positive symptoms through antagonism of DA-D2 receptors,
278 pilepsy and the relationship of negative and positive symptoms to cognition, quantitative magnetic re
284 as seen when the Scale for the Assessment of Positive Symptoms was used but not when the Positive and
286 work for the EOS patients with predominantly positive symptom were highly similar to typically develo
289 antipsychotic efficacy and those that model positive symptoms were employed and we found that L-Gova
290 nd bipolar disorder patients, the models for positive symptoms were largely non-overlapping between t
293 elations in a subgroup of patients with high positive symptoms were significantly reduced from age 14
294 1)H-MRSI) and rating scales for negative and positive symptoms were used to study 36 patients with sc
296 ent as a complex combination of negative and positive symptoms, which vary enormously from individual
297 associated with more hallucinations and more positive symptoms, while lower relative glucose metaboli
298 fects in individual patients correlated with positive symptoms, while the pattern similarity to NMDA
299 -0.126; 95% CI, -0.190 to -0.062; P < .001); positive symptoms with work skills (B, -0.059; 95% CI, -