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1 erences may underlie the observed pattern of neuroanatomic abnormalities and contribute to the specif
2 dhood, and consider the relationship between neuroanatomic abnormalities and the cognitive profile of
3  were generally underpowered to characterize neuroanatomic abnormalities associated with psychosis in
4  in length exhibit late-onset behavioral and neuroanatomic abnormalities consistent with HD.
5      The purpose of this study was to assess neuroanatomic abnormalities in children and adolescents
6 cations for understanding sex differences in neuroanatomic abnormalities in regions associated with p
7                                              Neuroanatomic abnormalities in schizophrenia may underli
8 netrant deletion was associated with similar neuroanatomic abnormalities to idiopathic schizophrenia.
9 ted cohorts at high risk for ASD, reciprocal neuroanatomic abnormalities were found and determined to
10 s and progressive behavioral, locomotor, and neuroanatomic abnormalities.
11 onmental stress of prematurity would promote neuroanatomic abnormality in individuals genetically vul
12  (MRIs), reflects how individual patterns of neuroanatomic aging deviate from their typical trajector
13 (CA), can be estimated from MRIs to evaluate neuroanatomic aging in cognitively normal (CN) individua
14 sectional measure that summarizes cumulative neuroanatomic aging since birth.
15                           We examine whether neuroanatomic alterations are 1) consistently observed i
16 udies selected for inclusion in this review, neuroanatomic alterations emerged across regions that ar
17 tion of cannabis may be linked to persistent neuroanatomic alterations typically seen in regular cann
18 or complex visual hallucinations may lead to neuroanatomic ambiguity, and elevated intracranial press
19  analysis of individual synaptic triads with neuroanatomic analyses and multiphoton live imaging of d
20 r zone and rescued some, but not all, of the neuroanatomic and behavioral abnormalities characteristi
21 ut there are limited data on their long-term neuroanatomic and cognitive consequences.
22                                        These neuroanatomic and functional changes are associated with
23 orescein labeling of GSNs to determine their neuroanatomic and functional relationships with orexin n
24 orks are qualitatively consistent with known neuroanatomic and functional structures in the spinal co
25                                     However, neuroanatomic and molecular mechanisms are not fully und
26 a way that captures the relationship between neuroanatomic and neurocognitive aging.
27 tion measures and to examine correlates with neuroanatomic and neurophysiologic anomalies.
28       Cardiac dysfunction is associated with neuroanatomic and neuropsychological changes in aging ad
29 traits drawn from behavioral/neurocognitive, neuroanatomic, and transcriptomic phenotypic domains, we
30  reduced hippocampal volume, indicating that neuroanatomic anomalies associated with depression may p
31 ods and connectivity data provide a putative neuroanatomic architecture for the integration of arousa
32 s and establish clinical, neurocognitive and neuroanatomic associations with increased inflammatory a
33                                          The neuroanatomic basis for this oro-facial coordination is
34                           In this study, the neuroanatomic basis of empathy was investigated in 123 p
35                         Although much of the neuroanatomic basis of visuomotor transformations has be
36 nd episodic memory decline mediated by early neuroanatomic biomarkers of Alzheimer's disease', by You
37 entify vulnerable networks without regard to neuroanatomic boundaries.
38                                     Abnormal neuroanatomic brain networks have been reported in schiz
39 ion in brain aging also map onto patterns of neuroanatomic change that reflect cognitive decline.
40            Sexual dimorphism in drug-related neuroanatomic changes and brain-behavior relationships m
41 ort the importance of prospectively studying neuroanatomic changes in bipolar disorder.
42 ental animal models, chronic stress leads to neuroanatomic changes in the hippocampus, in particular
43 ter perinatal stress and are associated with neuroanatomic changes in the perinatal period.
44                         Here we identify the neuroanatomic changes that are shared by 22 OCD adult an
45 science, ranging from neurophysiological and neuroanatomic characterizations to questions about neura
46 several neurotransmitters within one or more neuroanatomic circuits.
47 ins indicated that the degree of within-pair neuroanatomic concordance varied with brain region.
48 ns of HSV infection are considered here in a neuroanatomic context.
49 ure apraxia of speech clearly exists, with a neuroanatomic correlate of superior lateral premotor and
50                               To examine the neuroanatomic correlates of impaired self-awareness, dis
51                                          The neuroanatomic correlates of such changes are not fully k
52   Frequency of itching in FTLD-SD and AD and neuroanatomic correlates.
53 developing youth, we demonstrate dissociable neuroanatomic correlations that parallel those found in
54 at have the largest voxel-based or ROI-based neuroanatomic coverage.
55 and SNP-sets, whose effects have the largest neuroanatomic coverage.
56 s that have genetic effects with the largest neuroanatomic coverage.
57 tein E receptor 2 (ApoER2) exhibit identical neuroanatomic defects in laminar structures throughout t
58  results in ataxic mice that exhibit several neuroanatomic defects reminiscent of reeler.
59                                              Neuroanatomic deficiencies in limbic structures suggest
60               These studies delineate normal neuroanatomic development and can be used to understand
61 ng and diffusion tensor imaging to determine neuroanatomic differences between stress-susceptible and
62  in unawareness of illness in schizophrenia, neuroanatomic differences have not been examined.
63                                Investigating neuroanatomic differences in monozygotic twins who are d
64                           In this study, the neuroanatomic distribution of CRF1 and CRF2 receptor bin
65                                          The neuroanatomic distribution of these metabolites could he
66                                          The neuroanatomic distribution of this CRF receptor family m
67 of ischemia alone on brain NAD(H) levels and neuroanatomic distribution.
68                                              Neuroanatomic documentation of a delay in regional corti
69 associated with psychosis in 22q11DS, and/or neuroanatomic effects of variability in deletion size.
70                                              Neuroanatomic effects seemed fixed and non-progressive,
71  critical first steps are identifying where (neuroanatomic effects), when (timepoint in the lifespan)
72 uthors sought to examine the symptomatic and neuroanatomic effects, in young adulthood, of exposure t
73 s approach, we search for neurocognitive and neuroanatomic endophenotypes for schizophrenia in large
74 dentification of Glut4 neurons as a distinct neuroanatomic entity with a likely metabolic role.
75                                              Neuroanatomic evaluation of the MGC revealed that the do
76                                 There was no neuroanatomic evidence that AhR is preferentially coloca
77                          We have studied the neuroanatomic extent of electroconvulsive (ECS)-responsi
78 l months) resulting from the combinations of neuroanatomic feature, cortical layer, and brain cytoarc
79 n individual measurements of six microscopic neuroanatomic features for each of six cortical layers i
80 sorder, and that pretreatment alterations in neuroanatomic features predicted treatment outcome and w
81 les is accounted for by the six microscopic, neuroanatomic features.
82                   These results suggest that neuroanatomic FG abnormalities underlie at least some of
83               These convergent cognitive and neuroanatomic findings in individuals with a CSF molecul
84  were manually reconstructed within a common neuroanatomic framework, forming a cortico-cortical conn
85  evaluated systematically and according to a neuroanatomic framework.
86                         First, using in vivo neuroanatomic imaging on 14 pairs of monozygotic twins (
87 with ADHD), most with cognitive assessments, neuroanatomic imaging, and imaging of white matter tract
88                                         This neuroanatomic information provides important clues as to
89 m relatively poorly on new data or that lack neuroanatomic interpretability.
90 unction was used to transform all FreeSurfer neuroanatomic labels into PET image space, which were su
91 of the human brain lesion and the behavioral neuroanatomic literatures, may help to explain some of t
92 notypes varies from genetic data, structural neuroanatomic localization, immune markers, brain physio
93 however, are coarse-grained and lack precise neuroanatomic localization.
94            Gadolinium concentrations in both neuroanatomic locations were higher in linear GBCA-expos
95 alence are represented in spatially distinct neuroanatomic loci within the lateral horn.
96                These findings point toward a neuroanatomic locus for economic rationality in the agin
97 children participated in the study, with 837 neuroanatomic magnetic resonance images acquired longitu
98 l thickness were determined in vivo from 764 neuroanatomic magnetic resonance images acquired longitu
99 f 193 typically developing children with 389 neuroanatomic magnetic resonance images and varying leve
100 ents (mean 23.8 years, SD 4.3) with repeated neuroanatomic magnetic resonance imaging.
101 osum may thus provide an easily identifiable neuroanatomic marker to screen individuals possessing a
102                       First, we investigated neuroanatomic markers of familial predisposition by comp
103 d oxytocin receptor protein with established neuroanatomic methods.
104 ese data enable us to propose a componential neuroanatomic model of action that delineates the specif
105               Here we present evidence for a neuroanatomic model of conceptual combination from three
106                                  Theoretical neuroanatomic models of posttraumatic stress disorder (P
107 antic representation of "plaid jacket." Many neuroanatomic models of semantic memory propose that het
108  severity consistent with current functional neuroanatomic models of this disorder.
109           Consistent with current functional neuroanatomic models, patients with PTSD exhibited alter
110  adolescents were genotyped and had repeated neuroanatomic MRI (total 530 scans).
111 in cortical thickness was estimated from two neuroanatomic MRI scans in 43 youths with ADHD.
112 ologic (n = 5-6 animals, 21-25 cells/group), neuroanatomic (n = 6-8/group), and behavioral (n = 12/gr
113 ance imaging of the human brain to study the neuroanatomic network involved in aversive conditioning
114 bipolar and healthy youth and for changes in neuroanatomic network metrics following treatment in the
115                                   Converging neuroanatomic, neurophysiological, and neurobehavioral e
116 g to identify the potential relation between neuroanatomic or neurophysiologic abnormalities and cogn
117 s is the first in a series of reports on the neuroanatomic organization and connectivity of the macaq
118             To gain further insight into the neuroanatomic organization of the DRN, neuronal populati
119  The lattice-like grid is a novel functional/neuroanatomic organization that is ideal for distributin
120 d from structural MRI scans, and whole-brain neuroanatomic organization was compared across the parti
121                                          The neuroanatomic organizing principles underlying integrati
122                          In order to map the neuroanatomic origins of the complex neuropsychiatric be
123                             Changes in these neuroanatomic parameters were correlated with improvemen
124 he detection of abnormalities in fundamental neuroanatomic parameters.
125                    Continuing to clarify the neuroanatomic pathways in autistic spectrum disorders co
126 red with healthy controls, in near-identical neuroanatomic patterns.
127 lassified with 93.8% accuracy based on these neuroanatomic patterns.
128 nces in clinical phenotype to differences in neuroanatomic phenotype.
129 could be implemented via a direct functional neuroanatomic projection between IFC and STN (a "hyperdi
130 s nonuniformly distributed across strain and neuroanatomic region, suggesting certain organizing prin
131 vide potential treatment targets in distinct neuroanatomic regions during multifocal neurological dis
132 grammar, which have been closely linked with neuroanatomic regions for which sex differences have bee
133                Results Tissues from the four neuroanatomic regions of gadodiamide-exposed patients co
134         Astrocyte-specific RNAs from various neuroanatomic regions were attained using RiboTag techno
135 ced gene expression changes differed between neuroanatomic regions when comparing astrocytes from spi
136 identify the volume and mean thickness of 34 neuroanatomic regions.
137 ed the potential mediating role of increased neuroanatomic risk of Alzheimer's disease associated wit
138                            We found a robust neuroanatomic signature of 22q11DS, and the first eviden
139 s of the apolipoprotein E gene have distinct neuroanatomic signatures, identifiable in childhood.
140 h have unexploited potential to identify the neuroanatomic sites of drug action.
141 htly delayed compared with that described in neuroanatomic specimens.
142           These results suggest that certain neuroanatomic structures may be associated with attentio
143 veal that measures of inhibition covary with neuroanatomic structures previously identified as sensit
144 ectrode recordings enable the delineation of neuroanatomic structures.
145 ate quantitative estimates of objects within neuroanatomic structures.
146                            From the earliest neuroanatomic studies of reeler, it was anticipated that
147                                              Neuroanatomic studies of schizophrenia have reported tem
148                                              Neuroanatomic studies with magnetic resonance (MR) imagi
149 ere compared with the GA guidelines based on neuroanatomic studies.
150 gap junction proteins Cx26 and Cx32 form the neuroanatomic substrate for this gap junctional communic
151 erences in behavior are extensive, but their neuroanatomic substrate is unclear.
152 nown to influence sleep-wake regulation, the neuroanatomic substrate(s) mediating these effects remai
153 ymptoms and 22q11DS suggest partially shared neuroanatomic substrates.
154 ave the potential to further define critical neuroanatomic targets of drug action.
155                          Using computational neuroanatomic techniques, we estimated cortical thicknes
156 ferent terminals that express GluR5/6/7, two neuroanatomic tracers were injected in the sciatic nerve
157 e spinal cord to the brain, as determined by neuroanatomic tracing and behavioral testing.
158                                              Neuroanatomic tracing and immunohistochemistry were used
159                           By identifying the neuroanatomic variability in 22q11.2DS, and the separate
160           Purpose To provide a benchmark for neuroanatomic variability in clinically acquired brain M
161                                     Although neuroanatomic variation in this network was also heritab
162 n therapy or drug dose had a major impact on neuroanatomic volumes.
163 in geriatric depression and suggest possible neuroanatomic vulnerabilities to developing particular n

 
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