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Nora D. Volkow

Researcher at National Institute on Drug Abuse

Publications -  1038
Citations -  121498

Nora D. Volkow is an academic researcher from National Institute on Drug Abuse. The author has contributed to research in topics: Dopamine & Addiction. The author has an hindex of 165, co-authored 958 publications receiving 107463 citations. Previous affiliations of Nora D. Volkow include National Institutes of Health & North Shore University Hospital.

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Book ChapterDOI

PET imaging for addiction medicine: From neural mechanisms to clinical considerations.

TL;DR: Positron emission tomography (PET) has been shown to be an effective imaging technique to study neurometabolic and neurochemical processes involved in addiction as mentioned in this paper, which has been used to research neurobiological differences in substance abusers versus healthy controls and the pharmacokinetics and pharmacodynamics of abused drugs.
Journal ArticleDOI

Strategy for the formation of parametric images under conditions of low injected radioactivity applied to PET studies with the irreversible monoamine oxidase A tracers [11C]clorgyline and deuterium-substituted [11C]clorgyline.

TL;DR: A strategy was devised to reduce noise in the generation of parametric images of the model term related to enzyme or receptor concentration that should be generalizable to other tracers and should facilitate the analysis of group differences.
Journal ArticleDOI

Species differences in [11C]clorgyline binding in brain.

TL;DR: A species difference in the susceptibility of MAO A to inhibition by clorgyline is suggested and represents an unusual example of where the behavior of a radiotracer in the baboon brain does not predict its behavior in the human brain.
Journal ArticleDOI

Evidence that Ginkgo biloba extract does not inhibit MAO A and B in living human brain.

TL;DR: Ginkgo biloba administration did not produce significant changes in brain MAO A or MAO B suggesting that mechanisms other than MAO inhibition need to be considered as mediating some of its CNS effects.
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Obesity-resistant S5B rats showed greater cocaine conditioned place preference than the obesity-prone OM rats.

TL;DR: The results indicated that obesity-resistant S5B rats showed greater cocaine CPP than the obesity-prone OM rats, and showed that BC reduced cocaine conditioning effects supporting at least a partial regulatory role of D2R in conditioned responses to drugs.