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Autor:
Arthur W. Toga, Paul M. Thompson, Ming Chang Chiang, Agatha D. Lee, Debra L. Mills, Allan L. Reiss, Albert M. Galaburda, Julie R. Korenberg, Ursula Bellugi
Publikováno v:
NeuroImage. 36(4)
Williams syndrome (WS) is a neurodevelopmental disorder associated with deletion of approximately 20 contiguous genes in chromosome band 7q11.23. Individuals with WS exhibit mild to moderate mental retardation, but are relatively more proficient in s
Autor:
Bhooma Srinivasaraghavan, Diane Cookfair, Michael G. Dwyer, Ralph H.B. Benedict, Christopher W. Tjoa, Dominic A. Carone, Robert Zivadinov
Publikováno v:
NeuroImage. 29(2)
In multiple sclerosis (MS), atrophy occurs in various cortical and subcortical regions. However, it is unclear whether this is mostly due to gray (GM) or white matter (WM) loss. Recently, a new semi-automatic brain region extraction (SABRE) technique