Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Matthew H. Gnirke"'
Autor:
Moeed R. Chohan, Kevin M. Antshel, Matthew H. Gnirke, Zora Kikinis, Wendy R. Kates, Ioana L. Coman, Frank A. Middleton, Petya D. Radoeva, Matthew D. Perlstein, Martha E. Shenton, Wanda Fremont
Publikováno v:
Schizophrenia Research. 152:117-123
This study utilized diffusion tensor imaging (DTI) to analyze white matter tractography in the anterior limb of the internal capsule (ALIC), fornix, and uncinate fasciculus (UF) of individuals with 22q11.2 deletion syndrome and controls. Aberrations
Autor:
Kevin M. Antshel, Wendy R. Kates, Frank A. Middleton, Robert J. Shprintzen, Ioana L. Coman, Matthew H. Gnirke, Anne Marie Higgins, Wanda Fremont
Publikováno v:
NeuroImage. 53:1043-1050
Velo-cardio-facial syndrome (VCFS) is caused by a micro-deletion of over 40 genes at the q11.2 locus of chromosome 22 and is a risk factor for the development of schizophrenia and other psychiatric disorders. COMT, one of the genes located in the del
Autor:
Ioana L. Coman, Petya D. Radoeva, Amy K. Olszewski, Martha E. Shenton, Kevin M. Antshel, Frank A. Middleton, Joshua Nelson, Wendy R. Kates, Matthew H. Gnirke, Zora Kikinis, Wanda Fremont
Publikováno v:
Schizophrenia research. 161(1)
article i nfo Background: The 22q11.2 deletion syndrome (22q11.2DS) is regarded as an etiologically homogenous model for understanding neuroanatomic disruptions associated with a high risk for schizophrenia. This study utilized diffusion tensor imagi