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1 st step in the processes of 'sentience' and 'irritability'.
2 ued all study drugs due to an adverse event (irritability).
3 and libido, and with anorexia, fatigue, and irritability.
4 ying the sensitisation of C-fibres in airway irritability.
5 disordered breathing and reduces ventricular irritability.
6 tems related to anger, worry, dysphoria, and irritability.
7 ious mood symptoms, ie, sadness, crying, and irritability.
8 stories of impulsive aggressive behavior and irritability.
9 es were associated with decreasing levels of irritability.
10 ver, tachycardia, poor perfusion, and severe irritability.
11 pattern associated with abnormal electrical irritability; 13 patients had abnormal nerve conduction
13 .001), anxiety (3.00; 2.01-4.48; P < .001), irritability 2.99; 2.11-4.22; P < .001), and depression
14 crocephaly (41%), nausea and vomiting (30%), irritability (24%), and lethargy (21%) for children aged
15 performed in 45 patients with mTBI (38 with irritability, 32 with depression, and 18 with anxiety).
16 (48%), fatigue (46%), drowsiness (39%), and irritability (37%); most scores indicated high distress.
17 ), disinhibition (16% versus 2%, P = 0.009), irritability (48% versus 9%, P = 0.0001), sleep changes
18 stic specificity in the neural correlates of irritability, a symptom of both DMDD and bipolar disorde
21 five neuropsychiatric features: depression, irritability/aggression, obsessive/compulsive behaviours
23 vioral and psychophysiological correlates of irritability among children with severe mood dysregulati
24 ed in a sustained reduction in scores on the Irritability and Aggression subscales of the Overt Aggre
25 Given that psychiatric changes, including irritability and aggression, are common findings in HD p
26 dications are indicated for the treatment of irritability and agitation symptoms in children with aut
30 s analyses, the shared and unique effects of irritability and anxiety were tested on amygdala functio
31 2 major dimensions of child psychopathology, irritability and anxiety, on neural responses to facial
35 symptoms, including depressed mood, anxiety, irritability and craving in dependent subjects may contr
36 ) was significantly higher than that between irritability and delinquency (r(A)=0.57, 95% CI=0.45-0.6
37 ) was significantly higher than that between irritability and delinquency (r(A)=0.57, 95% CI=0.45-0.6
38 ic analyses, the genetic correlation between irritability and depression (r(A)=0.70, 95% CI=0.59-0.82
39 ic analyses, the genetic correlation between irritability and depression (r(A)=0.70, 95% CI=0.59-0.82
41 the hypothesis that the association between irritability and depression is accounted for by genetic
42 y exacerbate, or even cause symptoms such as irritability and depression that are common in early sta
44 nd bipolar disorder showed similar levels of irritability and did not differ from each other or from
45 uana relapse and reversed withdrawal-related irritability and disruptions in sleep and food intake (p
47 tween the two components of oppositionality (irritability and headstrong/hurtful behaviors) and depre
48 roversy exists regarding whether nonepisodic irritability and hyperarousal (severe mood dysregulation
49 severe mood dysregulation (i.e., nonepisodic irritability and hyperarousal without episodes of euphor
51 (PTE) affected speech processing, levels of irritability and hypertonicity, attention levels, abilit
53 side effects experienced by women using HC (irritability and lability) are not captured by a screeni
54 thic electromyogram with abnormal electrical irritability and muscle biopsy findings of myofibrillar
57 bacute encephalopathy with motor regression, irritability and stupor or coma resulting in major handi
58 that is, those who have severe, nonepisodic irritability and the hyperarousal symptoms characteristi
60 s known about genetic influences on juvenile irritability and whether such influences are development
64 equate growth, reduced reporting of colic or irritability, and a lower frequency of antibiotic use.
66 rted high levels of household strain, social irritability, and financial strain as well as limitation
71 ies as well as moderately strong links among irritability (anger), concentration deficits, and sleep
72 -sectional investigations and indicates that irritability/anger during MDEs is a highly prevalent cli
75 ion, included reductions in the frequency of irritability, anxiety, and delusions; among patients who
76 ower total withdrawal symptom score and less irritability, anxiety, craving, and restlessness than pl
79 lementary conceptualizations of pathological irritability are proposed: 1) aberrant emotional and beh
81 l models, the phenotypic association between irritability at wave 2 and depression at wave 3 was acco
83 ncy (beta -0.032, OR 1.10 [1.02-1.20]), more irritability (beta 0.032, OR 1.07 [1.01-1.14]), and more
85 y decreased locomotor activity and increased irritability but had no effect on sexual behavior, partn
87 tate cancer is followed by bowel and bladder irritability, by increasingly severe sexual dysfunction
88 cally and pathophysiologically distinct, yet irritability can be a clinical feature of both illnesses
89 Behavioral measures included locomotion, irritability, copulation, partner preference, and aggres
91 scent Development reported on the children's irritability, defined using a previously identified scal
93 sorder characterized by personality changes, irritability, depression, seizures, memory loss and some
94 ncluded dissociation and symptoms of "limbic irritability," depression, anxiety, and anger-hostility.
96 mine whether the neural mechanisms mediating irritability differ between bipolar disorder and DMDD, u
97 5% CI, 0.96-1.25] points; P = .02) and Anger/Irritability DRSP subscale score (1.22 [95% CI, 1.05-1.4
98 severe epilepsy including infantile spasms, irritability, failure to thrive, and stereotypic hand mo
99 = 9) presented in early infancy with severe irritability, followed by dystonia and stagnation of dev
100 growth restriction, infantile hypotonia, and irritability, followed by failure to thrive and short st
103 xiety (hazard ratio=1.87, 95% CI=1.28-2.73), irritability (hazard ratio=1.84, 95% CI=1.31-2.58), and
106 with behavioural disorders characterized by irritability, impulsiveness, bizarre alterations in dres
107 baseline emotional and behavioral disorders, irritability in adolescence predicted major depressive d
113 les, with new genetic risk factors affecting irritability in early and late adolescence for males.
114 ttle is known about the relationship between irritability in early life and its outcomes in mid-adult
116 community samples indicate that nonepisodic irritability in youths is common and is associated with
119 eficiency have included depression, anxiety, irritability, insomnia, weakness, diminished libido, imp
125 his study examines the extent to which youth irritability is related to adult psychiatric outcomes by
127 he Aberrant Behavior Checklist subscales for irritability, lethargy/social withdrawal, and hyperactiv
128 itioned to produce migraine symptoms such as irritability, loss of appetite, fatigue, depression, or
129 rvasive antisocial character traits, such as irritability, manipulativeness, and lack of remorse.
130 ype bipolar disorder, the pathophysiology of irritability may differ among the groups and is influenc
131 essed mothers with high anxious distress and irritability may require medications that reduce these s
132 arly perimenopausal women had higher odds of irritability, nervousness, and frequent mood changes but
133 ALS is characterised by personality change, irritability, obsessions, poor insight, and pervasive de
134 utward currents could also contribute to the irritability of the central nervous system typical of cl
135 reased rates of behavior problems, including irritability, oppositional defiant behavior, conduct dis
137 a extend prior work conducted in youths with irritability or anxiety alone and suggest that research
140 ome characterized by episodic acute onset of irritability or neurological deficits between 2 months a
141 od regulation problems in the form of either irritability or short episodes of mania-like symptoms in
142 regulation problems, such as severe chronic irritability or short episodes of mania-like symptoms, a
143 esses may be effective for cases with severe irritability or short episodes of mania-like symptoms.
144 he evidence base for the treatment of either irritability or short-lived episodes of mania-like sympt
145 characteristic of asthma is increased airway irritability, or bronchial hyperresponsiveness (BHR) whi
146 ania is accompanied by symptoms of euphoria, irritability, or excitation, whereas depression is assoc
147 uch as mood stabilizers, which dampen limbic irritability, or selective serotonin reuptake inhibitors
149 with a lower frequency of reported colic or irritability (P < 0.001) and a lower frequency of antibi
150 or nervousness (P<.02), depression (P<.03), irritability (P<.01), and the overall behavioral symptom
156 reduction in several core PMDD symptoms (ie, irritability, sadness, anxiety, food cravings, and bloat
157 ned as at least a 25 percent decrease in the Irritability score and a rating of much improved or very
158 resulted in a 56.9 percent reduction in the Irritability score, as compared with a 14.1 percent decr
159 al and genetic findings suggest that chronic irritability should be regarded as a mood problem that i
161 f frustration, children with severe, chronic irritability showed abnormally reduced activation in reg
162 terised by feelings of threat, restlessness, irritability, sleep disturbance, and tension, and sympto
163 degrees F, pericardial friction rub, patient irritability, small pericardial +/- pleural effusion.
164 search is needed to relate these findings to irritability specifically, rather than to other clinical
165 resulted in significant improvements on ABC irritability subscale (F = 6.80; p < .001; d = .96).
166 ry outcomes: the Aberrant Behavior Checklist-Irritability subscale (range, 0-45) and the Home Situati
168 At week 24, the Aberrant Behavior Checklist-Irritability subscale declined 47.7% in parent training
169 imary outcome measures were the score on the Irritability subscale of the Aberrant Behavior Checklist
170 l measure (Aberrant Behavior Checklist [ABC] irritability subscale) and safety measures were performe
172 Mood and behavioural symptoms, including irritability, tension, depressed mood, tearfulness, and
173 , the authors present a mechanistic model of irritability that integrates clinical and translational
174 ache, sleep disturbance, inability to relax, irritability) that does not resolve by resting or relaxi
175 athology during their lifetime, varying from irritability to psychosis, but prevalences of particular
176 tern of genetic and environmental effects on irritability using data from a prospective, four-wave lo
177 ith high levels of anxiety but low levels of irritability (Wald chi21 = 21.3; P < .001 for contrast).
179 premenstrual-related tiredness, sadness, and irritability were assessed twice over 6 years in 1,312 m
180 am, associations between neural activity and irritability were found more consistently in the DMDD gr
182 ociated with high levels of both anxiety and irritability, whereas increased connectivity was associa
184 othesized that during face emotion labeling, irritability would be associated with dysfunctional acti
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