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Basal ganglia glucose utilization after recent precentral ablation in the monkey

dc.contributor.authorDauth, George W.en_US
dc.contributor.authorGilman, Siden_US
dc.contributor.authorFrey, Kirk A.en_US
dc.contributor.authorPenney, John B.en_US
dc.date.accessioned2007-04-06T18:50:21Z
dc.date.available2007-04-06T18:50:21Z
dc.date.issued1985-05en_US
dc.identifier.citationDauth, George W.; Gilman, Sid; Frey, Kirk A; Penney, John B. (1985)."Basal ganglia glucose utilization after recent precentral ablation in the monkey." Annals of Neurology 17(5): 431-438. <http://hdl.handle.net/2027.42/50310>en_US
dc.identifier.issn0364-5134en_US
dc.identifier.issn1531-8249en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/50310
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=4004167&dopt=citationen_US
dc.description.abstractIn the macaque monkey, unilateral ablation of areas 4 and 6 of Brodmann result initially in a signficant decrease of glucose metabolic activity in the ipsilateral caudate nucleus, putamen, globus pallidus, substantia nigra, and subthalamic nucleus. The contralateral hemisphere shows nonsignificant but consistently decreased activity in the caudate nucleus, putamen, and globus pallidus. Cerebral blood flow is decreased in the same pattern as the glucose metabolic activity. The change in glucose metabolic activity result from loss of neurons known to project directly from the cerebral cortex to the basal ganglia and also from indirect effect(diaschisis) in basal ganglia structures that do not receive connections from the cerebral cortex.en_US
dc.format.extent1095893 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.publisherWiley Subscription Services, Inc., A Wiley Companyen_US
dc.subject.otherLife and Medical Sciencesen_US
dc.subject.otherNeuroscience, Neurology, and Psychiatryen_US
dc.titleBasal ganglia glucose utilization after recent precentral ablation in the monkeyen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelPsychiatryen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Neurology, The University of Michigan, Ann Arbor, MI 48109 ; University of Michigan, Department of Neurology, Neuroscience Laboratory Building, 1103 East Huron St, Ann Arbor, MI 48104en_US
dc.contributor.affiliationumDepartment of Neurology, The University of Michigan, Ann Arbor, MI 48109en_US
dc.contributor.affiliationumDepartment of Neurology, The University of Michigan, Ann Arbor, MI 48109en_US
dc.contributor.affiliationumDepartment of Neurology, The University of Michigan, Ann Arbor, MI 48109en_US
dc.identifier.pmid4004167en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/50310/1/410170503_ftp.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1002/ana.410170503en_US
dc.identifier.sourceAnnals of Neurologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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