Parieto-occipital grey matter abnormalities in children with Williams syndrome
about
Challenging the use of adult neuropsychological models for explaining neurodevelopmental disorders: developed versus developing brainsBridging the gene-behavior divide through neuroimaging deletion syndromes: Velocardiofacial (22q11.2 Deletion) and Williams (7q11.23 Deletion) syndromes.The effect of intellectual ability on functional activation in a neurodevelopmental disorder: preliminary evidence from multiple fMRI studies in Williams syndrome3D pattern of brain abnormalities in Williams syndrome visualized using tensor-based morphometry.Research Review: Williams syndrome: a critical review of the cognitive, behavioral, and neuroanatomical phenotype.Neural mechanisms in Williams syndrome: a unique window to genetic influences on cognition and behaviour.Morphometry of human insular cortex and insular volume reduction in Williams syndrome.Abnormal structure or function of the amygdala is a common component of neurodevelopmental disorders.Periventricular heterotopia in common microdeletion syndromesRearrangements of the Williams-Beuren syndrome locus: molecular basis and implications for speech and language development.Developmental profiles for multiple object tracking and spatial memory: typically developing preschoolers and people with Williams syndrome.Regional brain differences in cortical thickness, surface area and subcortical volume in individuals with Williams syndromeAn atypical 7q11.23 deletion in a normal IQ Williams-Beuren syndrome patient.Altered microstructure within social-cognitive brain networks during childhood in Williams syndrome.Object recognition in Williams syndrome: uneven ventral stream activation.Typical and atypical brain development: a review of neuroimaging studies.Electrophysiological study of local/global processing in Williams syndrome.Selective cerebral volume reduction in Rett syndrome: a multiple-approach MR imaging studyQuantitative analysis of gray and white matter in Williams syndromeGenetic contributions to white matter architecture revealed by diffusion tensor imaging in Williams syndromeResilience after 9/11: multimodal neuroimaging evidence for stress-related change in the healthy adult brainNeural phenotypes of common and rare genetic variants.A genetic model for understanding higher order visual processing: functional interactions of the ventral visual stream in Williams syndrome.MRI assessment of superior temporal gyrus in Williams syndrome.Visually guided step descent in children with Williams syndrome.Face repetition detection and social interest: An ERP study in adults with and without Williams syndrome.Surface-based morphometry reveals distinct cortical thickness and surface area profiles in Williams syndrome.Subjects with intellectual disability and familial need for full-time special education show regional brain alterations: a voxel-based morphometry study.Functional reorganization of the visual dorsal stream as probed by 3-D visual coherence in Williams syndrome.Socio-communicative deficits in young children with Williams syndrome: performance on the Autism Diagnostic Observation Schedule.Object-based mental rotation and visual perspective-taking in typical development and Williams syndrome.Learning without representational change: development of numerical estimation in individuals with Williams syndrome.
P2860
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P2860
Parieto-occipital grey matter abnormalities in children with Williams syndrome
description
im April 2006 veröffentlichter wissenschaftlicher Artikel
@de
scientific article published on 27 December 2005
@en
wetenschappelijk artikel
@nl
наукова стаття, опублікована у квітні 2006
@uk
name
Parieto-occipital grey matter abnormalities in children with Williams syndrome
@en
Parieto-occipital grey matter abnormalities in children with Williams syndrome
@nl
type
label
Parieto-occipital grey matter abnormalities in children with Williams syndrome
@en
Parieto-occipital grey matter abnormalities in children with Williams syndrome
@nl
prefLabel
Parieto-occipital grey matter abnormalities in children with Williams syndrome
@en
Parieto-occipital grey matter abnormalities in children with Williams syndrome
@nl
P2093
P50
P1433
P1476
Parieto-occipital grey matter abnormalities in children with Williams syndrome
@en
P2093
Brunelle F
Seidenwurm D
Zilbovicius M
P304
P356
10.1016/J.NEUROIMAGE.2005.10.051
P407
P577
2005-12-27T00:00:00Z