Frontostriatal deficits in fragile X syndrome: relation to FMR1 gene expression.
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Childhood developmental disorders: an academic and clinical convergence point for psychiatry, neurology, psychology and pediatricsFailing to deactivate: resting functional abnormalities in autismConceptualizing neurodevelopmental disorders through a mechanistic understanding of fragile X syndrome and Williams syndromePrefrontal social cognition network dysfunction underlying face encoding and social anxiety in fragile X syndromeSynaptic Plasticity, a Prominent Contributor to the Anxiety in Fragile X SyndromeStriatal Circuits as a Common Node for Autism PathophysiologyThe NIH Toolbox Cognitive Battery for intellectual disabilities: three preliminary studies and future directionsPrepulse inhibition in fragile X syndrome: feasibility, reliability, and implications for treatment.Aberrant face and gaze habituation in fragile x syndromeGene, brain, and behavior relationships in fragile X syndrome: evidence from neuroimaging studies.Open-label add-on treatment trial of minocycline in fragile X syndrome.On the role of the striatum in response inhibitionMorphometric spatial patterns differentiating boys with fragile X syndrome, typically developing boys, and developmentally delayed boys aged 1 to 3 yearsAffiliative behavior in Williams syndrome: social perception and real-life social behaviorDysregulated nitric oxide signaling as a candidate mechanism of fragile X syndrome and other neuropsychiatric disorders.Abnormal brain activation in neurofibromatosis type 1: a link between visual processing and the default mode network.Increasing our understanding of human cognition through the study of Fragile X Syndrome.Abnormal mGlu 5 receptor/endocannabinoid coupling in mice lacking FMRP and BC1 RNA.Genetic controls balancing excitatory and inhibitory synaptogenesis in neurodevelopmental disorder models.Discrimination learning and attentional set formation in a mouse model of Fragile X.Changes in sensitivity of reward and motor behavior to dopaminergic, glutamatergic, and cholinergic drugs in a mouse model of fragile X syndromeA phenotypic structure and neural correlates of compulsive behaviors in adolescentsFragile X syndrome: the GABAergic system and circuit dysfunction.Psychometric study of the Aberrant Behavior Checklist in Fragile X Syndrome and implications for targeted treatmentAutism Spectrum Disorder (ASD) and Fragile X Syndrome (FXS): Two Overlapping Disorders Reviewed through Electroencephalography-What Can be Interpreted from the Available Information?Structural and functional connectivity in the default mode network in 22q11.2 deletion syndrome.3D pattern of brain abnormalities in Fragile X syndrome visualized using tensor-based morphometry.Young adult male carriers of the fragile X premutation exhibit genetically modulated impairments in visuospatial tasks controlled for psychomotor speed.Fragile X-related proteins regulate mammalian circadian behavioral rhythms.Aberrant neural function during emotion attribution in female subjects with fragile X syndrome.Moving Toward Integrative, Multidimensional Research in Modern Psychiatry: Lessons Learned From Fragile X SyndromeDelineation of early attentional control difficulties in fragile X syndrome: focus on neurocomputational changes.The fragile X continuum: new advances and perspectives.Aberrant basal ganglia metabolism in fragile X syndrome: a magnetic resonance spectroscopy study.A quantitative ELISA assay for the fragile x mental retardation 1 protein.Early white-matter abnormalities of the ventral frontostriatal pathway in fragile X syndrome.Effects of stimulus salience on touchscreen serial reversal learning in a mouse model of fragile X syndrome.Neuroanatomy of fragile X syndrome is associated with aberrant behavior and the fragile X mental retardation protein (FMRP).A voxel-based morphometry comparison of regional gray matter between fragile X syndrome and autismInsights into brain development from neurogenetic syndromes: evidence from fragile X syndrome, Williams syndrome, Turner syndrome and velocardiofacial syndrome.
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P2860
Frontostriatal deficits in fragile X syndrome: relation to FMR1 gene expression.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on March 2004
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Frontostriatal deficits in fragile X syndrome: relation to FMR1 gene expression.
@en
Frontostriatal deficits in fragile X syndrome: relation to FMR1 gene expression.
@nl
type
label
Frontostriatal deficits in fragile X syndrome: relation to FMR1 gene expression.
@en
Frontostriatal deficits in fragile X syndrome: relation to FMR1 gene expression.
@nl
prefLabel
Frontostriatal deficits in fragile X syndrome: relation to FMR1 gene expression.
@en
Frontostriatal deficits in fragile X syndrome: relation to FMR1 gene expression.
@nl
P2093
P2860
P356
P1476
Frontostriatal deficits in fragile X syndrome: relation to FMR1 gene expression.
@en
P2093
P2860
P304
P356
10.1073/PNAS.0304544101
P407
P50
P577
2004-03-01T00:00:00Z