Literature DB >> 12488811

Morphology and morphometry of the corpus callosum in Williams syndrome: a T1-weighted MRI study.

F Tomaiuolo1, M Di Paola, B Caravale, S Vicari, M Petrides, C Caltagirone.   

Abstract

Williams syndrome (WS) is characterised by a defined genetic aetiology and a specific cognitive profile. It provides an opportunity to examine associations between neuroanatomy, behaviour, and genetics. High-resolution T1-weighted MRI of the brain of 12 patients with WS and 12 normal control subjects were used to estimate the shape and volume of the corpus callosum (CC), as well as the voxel intensity values as a measure its water content. The CC of patients with WS was more convex than that of normal control subjects and overall smaller in volume, particularly in the splenium and in the caudal part of the callosal body. In addition, there were higher ratio values of voxel intensity (i.e. less water content) in the mid-section of the body and the caudal part of the body of the CC. These combined features indicate an aberrant development of the CC in patients with WS and document some of the anatomical abnormalities that may underlie some of the cognitive impairments observed in subjects with WS.

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Year:  2002        PMID: 12488811     DOI: 10.1097/00001756-200212030-00022

Source DB:  PubMed          Journal:  Neuroreport        ISSN: 0959-4965            Impact factor:   1.837


  25 in total

1.  Gross morphology and morphometric sequelae in the hippocampus, fornix, and corpus callosum of patients with severe non-missile traumatic brain injury without macroscopically detectable lesions: a T1 weighted MRI study.

Authors:  F Tomaiuolo; G A Carlesimo; M Di Paola; M Petrides; F Fera; R Bonanni; R Formisano; P Pasqualetti; C Caltagirone
Journal:  J Neurol Neurosurg Psychiatry       Date:  2004-09       Impact factor: 10.154

2.  Callosal morphology in Williams syndrome: a new evaluation of shape and thickness.

Authors:  Eileen Luders; Margherita Di Paola; Francesco Tomaiuolo; Paul M Thompson; Arthur W Toga; Stefano Vicari; Michael Petrides; Carlo Caltagirone
Journal:  Neuroreport       Date:  2007-02-12       Impact factor: 1.837

3.  Genetic contributions to white matter architecture revealed by diffusion tensor imaging in Williams syndrome.

Authors:  Stefano Marenco; Michael A Siuta; J Shane Kippenhan; Samuel Grodofsky; Wei-Li Chang; Philip Kohn; Carolyn B Mervis; Colleen A Morris; Daniel R Weinberger; Andreas Meyer-Lindenberg; Carlo Pierpaoli; Karen Faith Berman
Journal:  Proc Natl Acad Sci U S A       Date:  2007-09-07       Impact factor: 11.205

4.  Probabilistic topography of human corpus callosum using cytoarchitectural parcellation and high angular resolution diffusion imaging tractography.

Authors:  Yi-Ping Chao; Kuan-Hung Cho; Chun-Hung Yeh; Kun-Hsien Chou; Jyh-Horng Chen; Ching-Po Lin
Journal:  Hum Brain Mapp       Date:  2009-10       Impact factor: 5.038

5.  MRI assessment of superior temporal gyrus in Williams syndrome.

Authors:  Adriana Sampaio; Nuno Sousa; Montse Férnandez; Cristiana Vasconcelos; Martha E Shenton; Oscar F Gonçalves
Journal:  Cogn Behav Neurol       Date:  2008-09       Impact factor: 1.600

Review 6.  Neural phenotypes of common and rare genetic variants.

Authors:  Carrie E Bearden; David C Glahn; Agatha D Lee; Ming-Chang Chiang; Theo G M van Erp; Tyrone D Cannon; Allan L Reiss; Arthur W Toga; Paul M Thompson
Journal:  Biol Psychol       Date:  2008-02-23       Impact factor: 3.251

Review 7.  Bridging the gene-behavior divide through neuroimaging deletion syndromes: Velocardiofacial (22q11.2 Deletion) and Williams (7q11.23 Deletion) syndromes.

Authors:  Daniel Paul Eisenberg; Mbemba Jabbi; Karen Faith Berman
Journal:  Neuroimage       Date:  2010-03-03       Impact factor: 6.556

8.  N-methyl-D-aspartate receptor-mediated axonal injury in adult rat corpus callosum.

Authors:  Jingdong Zhang; Jianuo Liu; Howard S Fox; Huangui Xiong
Journal:  J Neurosci Res       Date:  2012-11-14       Impact factor: 4.164

Review 9.  Copy number variants at Williams-Beuren syndrome 7q11.23 region.

Authors:  Giuseppe Merla; Nicola Brunetti-Pierri; Lucia Micale; Carmela Fusco
Journal:  Hum Genet       Date:  2010-05-01       Impact factor: 4.132

10.  Intracisternal Gtf2i Gene Therapy Ameliorates Deficits in Cognition and Synaptic Plasticity of a Mouse Model of Williams-Beuren Syndrome.

Authors:  Cristina Borralleras; Ignasi Sahun; Luis A Pérez-Jurado; Victoria Campuzano
Journal:  Mol Ther       Date:  2015-07-28       Impact factor: 11.454

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