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1 ice displayed reduced motor coordination and hyperactivity.
2 h the hyperflexible phenotype, and posterior hyperactivity.
3 ive (SH) rats, which are known to exhibit CB hyperactivity.
4 used PNEC hyperinnervation and nodose neuron hyperactivity.
5 romic defects, exhibit inner ear defects and hyperactivity.
6 n, highlighting a rigid, set mode of sensory hyperactivity.
7 by increased azoxystrobin uptake induced by hyperactivity.
8 rcuit dysfunction that is caused by cortical hyperactivity.
9 ase and thyroid stimulating hormone receptor hyperactivity.
10 In ClockDelta19 mice, AUT1 reversed hyperactivity.
11 state, and attenuated OBX-induced locomotor hyperactivity.
12 duced adult body mass, social avoidance, and hyperactivity.
13 disease of TSC1/TSC2 inactivation and mTORC1 hyperactivity.
14 imbic seizures can be supported by GABAergic hyperactivity.
15 s and risk of offspring conduct disorder and hyperactivity.
16 depending on the level and timing of mTORC1 hyperactivity.
17 [14%] of 610 siblings, p=0.010), inattention-hyperactivity (15 [19%] vs 86 [14%], p<0.0001), social w
18 ue to either Tbx1 or Slc12a2 mutations cause hyperactivity; (2) it is vestibular dysfunction, which f
19 lso necessary for inner ear function, causes hyperactivity; (2) vestibular rather than auditory failu
20 ciations with vision problems, microcephaly, hyperactivity, a tendency to obesity, and feeding diffic
21 renatal stress and both conduct disorder and hyperactivity, after adjusting for sex, parental educati
23 rather than socio-environmental reasons why hyperactivity and anxiety disorders occur at higher rate
24 rather than auditory dysfunction that causes hyperactivity and anxiety-related symptoms; and (3) the
25 e therapeutic strategy to reduce hippocampal hyperactivity and attenuate behavioral deficits in schiz
28 arly loss of entorhinal input on hippocampal hyperactivity and cognitive deficits characterizing earl
31 cortex-amygdala circuitry: intrinsic sensory hyperactivity and disinhibition give rise to frontal ove
33 11 years to concurrent anxiety, depression, hyperactivity and impulsivity, inattention, and conduct
34 6 years of age included anxiety, depression, hyperactivity and impulsivity, inattention, conduct prob
37 oc2a+/- fam57ba+/- double heterozygotes show hyperactivity and increased seizure susceptibility relat
38 the neuropeptide neuromedin U (Nmu) promotes hyperactivity and inhibits sleep in zebrafish larvae, wh
39 n the existing circuitry, reduce hippocampal hyperactivity and normalize aberrant dopamine neuron act
40 induced hypothalamic-pituitary-adrenal axis hyperactivity and reduced fear- and anxiety-related beha
42 characterized by a combination of functional hyperactivity and smaller gray matter volume compared wi
47 ults suggest an association between MeHg and hyperactivity, and imply that fish chronically exposed t
48 ities, including deficits in motor learning, hyperactivity, and increased risk-taking and self-injuri
50 (Mn) exposure with inattention, impulsivity, hyperactivity, and oppositional behaviors, but causal in
51 ) dose-dependently ameliorated PPI deficits, hyperactivity, and risk-taking behaviors, in a fashion a
54 stibular rather than auditory failure causes hyperactivity; and (3) the severity rather than the age
55 teraction, compulsive behaviors, aggression, hyperactivity, anxiety, depression, and somatosensory ga
56 t NOTCH2 signaling and consequent osteoclast hyperactivity are closely associated with the bone-relat
57 thoughts is also associated with hippocampal hyperactivity, arising from dysfunctional GABAergic inte
58 enhanced phasic dopamine release, behavioral hyperactivity, associative learning deficits, and a para
60 negative feedback loop that blocks neuronal hyperactivity at least partly through the inhibition of
61 to belong to the high symptom trajectory for hyperactivity (B = 0.46, p < .05) and conduct disorder (
62 ion-deficit/hyperactivity disorder symptoms (hyperactivity, but not inattention) on the basis of indi
63 we investigated to what extent blocking this hyperactivity can improve optogenetic retinal prosthetic
65 nmental exposures and children's inattention/hyperactivity, conduct problems, and educational achieve
67 mice, but it remains unclear whether kinase hyperactivity contributes to the behavioral phenotypes.
68 f the ClockDelta19 mouse is characterized by hyperactivity, decreased anxiety-like behavior, decrease
69 n the forebrain (Plcg1(f/f); CaMKII) exhibit hyperactivity, decreased anxiety-like behavior, reduced
70 r (94.2 [1.69]; P = .004), attention-deficit/hyperactivity disorder (96.3 [0.91]; P = .002), oppositi
73 PBDEs and intelligence or Attention Deficit/Hyperactivity Disorder (ADHD) and attention-related beha
74 opmental disorders such as attention deficit hyperactivity disorder (ADHD) and autism spectrum disord
75 d between extraversion and attention-deficit-hyperactivity disorder (ADHD) and between openness and s
77 been effective in treating attention-deficit/hyperactivity disorder (ADHD) and is currently the first
79 s used clinically to treat attention-deficit/hyperactivity disorder (ADHD) and off-label as a perform
80 m spectrum disorder (ASD), attention deficit hyperactivity disorder (ADHD) and schizophrenia (SCZ).
81 tric conditions, including attention deficit hyperactivity disorder (ADHD) and substance use disorder
82 n the relationship between attention-deficit hyperactivity disorder (ADHD) and younger relative age i
85 ated that individuals with attention-deficit/hyperactivity disorder (ADHD) are more likely to experie
87 adult outcome of childhood attention deficit hyperactivity disorder (ADHD) could guide novel interven
90 uestioned the stability of attention-deficit hyperactivity disorder (ADHD) from childhood to adulthoo
92 Neuroimaging studies of attention-deficit/hyperactivity disorder (ADHD) have most commonly reporte
93 ng (fMRI) studies of adult attention-deficit/hyperactivity disorder (ADHD) have revealed various ADHD
94 ences were associated with attention-deficit/hyperactivity disorder (ADHD) in a recent multi-site, me
95 medications used to treat attention-deficit/hyperactivity disorder (ADHD) increase sympathetic tone
103 Recognition that adult attention-deficit/hyperactivity disorder (ADHD) is common, seriously impai
105 pectrum disorder (ASD) and attention-deficit/hyperactivity disorder (ADHD) is increasingly appreciate
110 g adults without childhood attention deficit hyperactivity disorder (ADHD) often present to clinics s
113 d the effects of childhood attention deficit hyperactivity disorder (ADHD) symptoms, both inattention
114 rder, major depression and attention deficit hyperactivity disorder (ADHD) using genomic data from 15
116 g intellectual disability, attention deficit/hyperactivity disorder (ADHD), and autism spectrum disor
117 genetic susceptibility of Attention-Deficit/Hyperactivity Disorder (ADHD), but without much success.
118 oride for the treatment of attention-deficit/hyperactivity disorder (ADHD), little is known about age
120 ms of depression, anxiety, attention/deficit hyperactivity disorder (ADHD), oppositional defiant diso
121 ted behavioral hallmark of attention-deficit/hyperactivity disorder (ADHD), strongly influences addic
122 stand the underpinnings of attention-deficit/hyperactivity disorder (ADHD), we targeted the relations
123 ition is a core deficit of attention deficit hyperactivity disorder (ADHD), which is a common childho
124 ity among individuals with attention deficit hyperactivity disorder (ADHD), yet associations between
138 variant has been linked to attention-deficit/hyperactivity disorder (ADHD); however, the underlying m
140 3 [95% CI, 0.62-1.13]), or attention-deficit/hyperactivity disorder (HR, 0.99 [95% CI, 0.79-1.25]).
141 =3540), autism (N=16 146), attention-deficit/hyperactivity disorder (N=18 726) and affective disorder
144 ng infantile parkinsonism, attention-deficit/hyperactivity disorder and autism spectrum disorder.
145 ), behavioral disturbance (attention deficit hyperactivity disorder and conduct disorder), psychosis-
147 Some conditions, such as attention-deficit/hyperactivity disorder and inpatient well-newborn care,
148 schizophrenia, depression, attention-deficit hyperactivity disorder and substance abuse disorders.
151 gotic twins discordant for attention deficit hyperactivity disorder can elucidate mechanisms that con
152 of why many children with attention deficit hyperactivity disorder do not outgrow the disorder by ad
153 tensive drugs, sleep aids, attention-deficit/hyperactivity disorder drugs, and antidepressant drugs)
154 of insomnia [sleep aids], attention-deficit/hyperactivity disorder drugs, antidepressant drugs, and
156 2.02 [95% CI, 1.80-2.26]; attention-deficit/hyperactivity disorder HR, 2.21 [95% CI, 2.04-2.39]).
160 : 1.4, 7.7) higher odds of attention deficit/hyperactivity disorder problems compared with children w
161 itude) relates to specific attention-deficit/hyperactivity disorder symptoms (hyperactivity, but not
163 patient well-newborn care, attention-deficit/hyperactivity disorder, and asthma among all conditions.
164 , including schizophrenia, attention deficit/hyperactivity disorder, and autism spectrum disorders.
167 ric diagnosis of interest (attention-deficit/hyperactivity disorder, autism spectrum disorder, schizo
169 r clinical development for attention deficit hyperactivity disorder, binge eating disorder, cocaine a
170 moking with drug and AUDs, attention-deficit hyperactivity disorder, bipolar disorder and antisocial
171 diabetes, waist-hip ratio, attention deficit hyperactivity disorder, bipolar disorder, major depressi
172 ty in patients with autism/attention deficit hyperactivity disorder, compared with respective control
173 schizophrenia, depression, attention-deficit/hyperactivity disorder, eating disorders, autism spectru
174 ssociated with addiction, attention-deficit/ hyperactivity disorder, schizophrenia, and Parkinson's d
175 ture of DD overlapped with attention-deficit/hyperactivity disorder, schizophrenia, major depression,
176 autism spectrum disorders, attention deficit/hyperactivity disorder, severe learning disability, cere
177 of attention--symptoms of attention deficit hyperactivity disorder--from resting-state connectivity
192 to a novel compound phenotype consisting of hyperactivity, disrupted circadian behavior patterns, an
193 driving glutamate dysregulation and neuronal hyperactivity during AD.SIGNIFICANCE STATEMENT Neuronal
200 s with human studies, we discuss the circuit hyperactivity hypothesis for OCD, a potential circuitry
201 tting of lupus-like CD4 T cell-driven B cell hyperactivity, IL-21 signaling on Ag-specific donor CD8
202 nd found that losing this complex results in hyperactivity, impaired learning and memory, and abnorma
203 ibition of BACE activity can rescue neuronal hyperactivity, impaired long-range circuit function, and
204 iency in the Treg lineage resulted in immune hyperactivity, implicating Notch activity in Treg homeos
206 in female adolescents may be causal, whereas hyperactivity-impulsivity appears to act indirectly, thr
207 sorder (ADHD) symptoms, both inattention and hyperactivity-impulsivity, on the development of smoking
210 UT1 completely prevented amphetamine-induced hyperactivity in a dose-dependent manner, similar to the
212 le of both cholinergic sprouting and dentate hyperactivity in AD symptomatogenesis should be consider
213 The subsequent reconstitution of SC mTORC1 hyperactivity in adult animals resulted in focal hypermy
216 chronic pain in a rat SCI model depends upon hyperactivity in dorsal root ganglia (DRG) neurons.
228 t that the development of psychosis involves hyperactivity in the hippocampus that drives increased a
229 Compared with NTC, PTSD patients showed hyperactivity in the right anterior insula and bilateral
230 ects of different levels of sustained mTORC1 hyperactivity in the SC lineage, we disrupted negative r
233 onfidence interval (CI): 1.03, 1.20] and the hyperactivity-inattention subscale scores at 5 y (IRR: 1
234 , adolescents with high levels of conduct or hyperactivity/inattention symptoms who had also experien
237 The authors sought to explore how conduct, hyperactivity/inattention, and emotional symptoms are as
238 ficiency in asthmatic airways promotes Orai1 hyperactivity, increased ASM contraction and airway hype
239 mals displayed behavioural anomalies such as hyperactivity, increased time in the open arms of the el
241 es pathological sleepiness [1-4], whereas OH hyperactivity is associated with stress and anxiety [5-1
242 Further analysis revealed that this neuronal hyperactivity is driven by decreased background inhibiti
244 However, HA instillation ameliorated bladder hyperactivity, lessened bladder mucosa damage, and decre
246 dromal AD, we propose that this APOE4-driven hyperactivity may be a causative factor driving increase
247 sensitivity achieved by blocking spontaneous hyperactivity may extend the dynamic range of optogeneti
251 ein, we demonstrated that overactivation and hyperactivity of FRS2alpha, as well as overexpression of
253 pancreatic cancer development by sustaining hyperactivity of multiple oncogenic signaling pathways,
255 eater number of stressful life events showed hyperactivity of the amygdala and several regions across
257 on of local ATP microgradients caused by the hyperactivity of the hippocampal network, at least in th
259 se hunger-display electrical and biochemical hyperactivity on exposure to dietary doses of ethanol in
260 estibular dysfunction differentiates whether hyperactivity or anxiety co-occurs with inner ear dysfun
261 f vestibular dysfunction can predict whether hyperactivity or anxiety coexist with inner ear dysfunct
263 resulted in behaviors that recapitulate the hyperactivity phenotype caused by absence of maternal re
264 iety-like behavior, but resulted in a robust hyperactivity phenotype in novel and home cage environme
265 Here, we have identified an APOE4-associated hyperactivity phenotype in the brains of aged APOE mice
266 lted in more pronounced social avoidance and hyperactivity, phenotypes not abrogated by cross-fosteri
267 suggested that the pathological spontaneous hyperactivity present in dystrophic retinas may contribu
269 term for the syndrome-paroxysmal sympathetic hyperactivity (PSH)-and clear diagnostic criteria define
270 function results in consistent microcephaly, hyperactivity, reduced anxiety, and deficient spatial le
271 (2)) conferred increased risk of inattention-hyperactivity (relative risk [RR] 1.53, 95% CI 1.13-2.08
272 at a cloned alpha-like BiOctR also induced a hyperactivity response in Balanus cyprids mediated by th
273 The change in parent-rated inattention and hyperactivity scores over the first 3 months of MPH medi
274 monstrate that inhibition of mGluR5 corrects hyperactivity, seizures, and elevated de novo synaptic p
275 ay aberrant behavioral phenotypes, including hyperactivity, social interaction deficits, and increase
276 their activity in favor of pyramidal neuron hyperactivity: somatostatin-expressing and parvalbumin-e
277 on of cortical GABAergic neurons may lead to hyperactivity states such as seizures or contribute to t
278 main body cell fate determinant Eya, and Wnt hyperactivity strongly biases cells towards polar and st
279 1 years of age using a screening instrument (hyperactivity subscale of the Strength and Difficulties
280 odromal Syndromes, and for attention-deficit/hyperactivity, substance-related, and mood disorders.
281 rder (n = 25) demonstrated intrinsic sensory hyperactivity (suppressed posterior alpha power, source-
283 isk ratio [RR], 1.42; 95% CI, 1.25-1.62) and hyperactivity symptoms (RR, 1.31; 95% CI, 1.16-1.49), wh
286 brain injury develop a state of sympathetic hyperactivity that can persist for weeks or months, cons
287 nitus may play a role in auditory and limbic hyperactivity, the non-auditory effects of blast and pot
288 m trajectories of 1) conduct disorder and 2) hyperactivity throughout childhood, identified using lat
289 episodes of dramatic behavioral changes from hyperactivity to "depression-like" behavior, suggestive
290 rect evidence linking locus coeruleus system hyperactivity to PTSD hyperresponsiveness is sparse.
292 ese were improved after blocking spontaneous hyperactivity using meclofenamic acid, a gap junction bl
293 failed to inhibit conditioned avoidance and hyperactivity using pharmacological and transgenic model
294 on (1.34 ng/bee) impaired locomotion, caused hyperactivity (velocity: +109%; time moving: +44%) short
295 emory, executive function, and attention and hyperactivity, were assessed at baseline and postinterve
296 on-free samples were characterized by limbic hyperactivity, whereas no such group differences were fo
297 gher in visual cortex of MAM rats (posterior hyperactivity), which might parallel perceptual problems
298 n Shank3 (Shank3B(-/-)) shows early cortical hyperactivity, which triggers increased SPN excitatory s
299 e-treated rats exhibited significant bladder hyperactivity with an increase in micturition frequency
300 from immunocomplex deposition due to B cell hyperactivity with increased risk for B cell lymphoma de
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