White matter microstructural abnormalities in girls with chromosome 22q11.2 deletion syndrome, Fragile X or Turner syndrome as evidenced by diffusion tensor imaging

NeuroImage

Volumn 81, Issue , 2013, Pages 441-454

  Villalon Reina, Julio ^a   Jahanshad, Neda ^a   Beaton, Elliott ^d   Toga, Arthur W ^a   Thompson, Paul M ^a   Simon, Tony J ^b,c  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

^c UNIVERSITY OF CALIFORNIA   (United States)

^d UNIVERSITY OF NEW ORLEANS   (United States)

Author keywords

Connectivity; Diffusion tensor imaging; Genetic diseases; Neurodevelopmental diseases

Indexed keywords

ADOLESCENT; AGE DISTRIBUTION; ARTICLE; CAPSULA INTERNA; CEREBELLAR PEDUNCLE; CHILD; CHROMOSOME 22Q11.2 DELETION SYNDROME; CHROMOSOME DELETION 22Q11; CONTROLLED STUDY; CORPUS CALLOSUM; DIFFUSION TENSOR IMAGING; FEMALE; FRACTIONAL ANISOTROPY; FRAGILE X SYNDROME; HUMAN; HUMAN TISSUE; IMAGE PROCESSING; INFERIOR LONGITUDINAL BUNDLE; LEFT CEREBELLAR PEDUNCLE; MAJOR CLINICAL STUDY; NERVE TRACT; PRIMARY MOTOR CORTEX; PRIORITY JOURNAL; PYRAMIDAL TRACT; RIGHT INTERNAL CAPSULE; SCHOOL CHILD; SUPERIOR LONGITUDINAL BUNDLE; THALAMUS POSTERIOR NUCLEUS; TURNER SYNDROME; VOXEL BASED MORPHOMETRY; WHITE MATTER LESION; ANISOTROPY; BRAIN; COMPUTER ASSISTED DIAGNOSIS; MYELINATED NERVE; PATHOLOGY;

22Q11 DELETION SYNDROME; ADOLESCENT; ANISOTROPY; BRAIN; CHILD; DIFFUSION TENSOR IMAGING; FEMALE; FRAGILE X SYNDROME; HUMANS; IMAGE INTERPRETATION, COMPUTER-ASSISTED; NERVE FIBERS, MYELINATED; NEURAL PATHWAYS; TURNER SYNDROME;

EID: 84879486428     PISSN: 10538119     EISSN: 10959572     Source Type: Journal    
DOI: 10.1016/j.neuroimage.2013.04.028     Document Type: Article

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