Brain abnormalities in Williams syndrome (WS) have been consistently reported, despite few studies have devoted attention to connectivity between different brain regions in WS. In this study, we evaluated corpus callosum (CC) morphometry: bending angle, length, thickness and curvature of CC using a new shape analysis method in a group of 17 individuals with WS matched with a typically developing group. We used this multimethod approach because we hypothesized that neurodevelopmental abnormalities might result in both volume changes and structure deformation. Overall, we found reduced absolute CC cross-sectional area and volume in WS (mean CC and subsections). In parallel, we observed group differences regarding CC shape and thickness. Speci...
m of this study was to evaluate the frequency of callosal abnormalities and white matter alterations...
m of this study was to evaluate the frequency of callosal abnormalities and white matter alterations...
We identified and mapped an anatomically localized failure of cortical maturation in Williams syndro...
We applied novel mesh-based geometrical modeling methods to calculate and compare the thickness of t...
We applied novel mesh-based geometrical modeling methods to calculate and compare the thickness of t...
We applied novel mesh-based geometrical modeling methods to calculate and compare the thickness of t...
We applied novel mesh-based geometrical modeling methods to calculate and compare the thickness of t...
Williams syndrome is a neurodevelopmental genetic disorder caused by a hemizygous deletion on chromo...
Williams syndrome is a neurodevelopmental genetic disorder caused by a hemizygous deletion on chromo...
BACKGROUND AND PURPOSE: The corpus callosum (CC) consists of topographically arranged white matter (...
Background:As a neurobehavioral disorder with a spe-cific neurocognitive profile and awell-defined g...
Williams syndrome (WS) is a neurodevelopmental disorder associated with deletion of ∼20 contiguous g...
Background: We investigated structural brain morphology of intellectually disabled children with Wil...
m of this study was to evaluate the frequency of callosal abnormalities and white matter alterations...
BACKGROUND AND PURPOSE: Variable alterations to the structure of the corpus callosum have been descr...
m of this study was to evaluate the frequency of callosal abnormalities and white matter alterations...
m of this study was to evaluate the frequency of callosal abnormalities and white matter alterations...
We identified and mapped an anatomically localized failure of cortical maturation in Williams syndro...
We applied novel mesh-based geometrical modeling methods to calculate and compare the thickness of t...
We applied novel mesh-based geometrical modeling methods to calculate and compare the thickness of t...
We applied novel mesh-based geometrical modeling methods to calculate and compare the thickness of t...
We applied novel mesh-based geometrical modeling methods to calculate and compare the thickness of t...
Williams syndrome is a neurodevelopmental genetic disorder caused by a hemizygous deletion on chromo...
Williams syndrome is a neurodevelopmental genetic disorder caused by a hemizygous deletion on chromo...
BACKGROUND AND PURPOSE: The corpus callosum (CC) consists of topographically arranged white matter (...
Background:As a neurobehavioral disorder with a spe-cific neurocognitive profile and awell-defined g...
Williams syndrome (WS) is a neurodevelopmental disorder associated with deletion of ∼20 contiguous g...
Background: We investigated structural brain morphology of intellectually disabled children with Wil...
m of this study was to evaluate the frequency of callosal abnormalities and white matter alterations...
BACKGROUND AND PURPOSE: Variable alterations to the structure of the corpus callosum have been descr...
m of this study was to evaluate the frequency of callosal abnormalities and white matter alterations...
m of this study was to evaluate the frequency of callosal abnormalities and white matter alterations...
We identified and mapped an anatomically localized failure of cortical maturation in Williams syndro...