Defining structural, functional, and chemical abnormalities with in vivo neuroimaging
methods has been a mainstay of depression research for more than 20 years (reviewed
in
Drevets 2000
,
Mayberg 2003
). Recent studies have both replicated and extended previous findings by capitalizing
on advances in imaging physics, analytic strategies, and the growing ease of acquiring
complementary structural and functional studies in the same individual. The field
has further matured to now emphasize more than just individual regions but also their
organization within integrated pathways and distributed neural networks (
Anand et al 2005
;
Drevets 1999
,
Mayberg 1997
;
Seminowicz et al 2004
).To read this article in full you will need to make a payment
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