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Motor dysfunction in olivopontocerebellar atrophy is related to cerebral metabolic rate studied with positron emission tomography

dc.contributor.authorRosenthal, Guyen_US
dc.contributor.authorGilman, Siden_US
dc.contributor.authorKoeppe, Robert A.en_US
dc.contributor.authorKluin, Karen J.en_US
dc.contributor.authorMarkel, Dorene S.en_US
dc.contributor.authorJunck, Larryen_US
dc.contributor.authorGebarski, Stephen S.en_US
dc.date.accessioned2007-04-06T18:52:09Z
dc.date.available2007-04-06T18:52:09Z
dc.date.issued1988-09en_US
dc.identifier.citationRosenthal, Guy; Gilman, Sid; Koeppe, Robert A.; Kluin, Karen J.; Markel, Dorene S.; Junck, Larry; Gebarski, Stephen S. (1988)."Motor dysfunction in olivopontocerebellar atrophy is related to cerebral metabolic rate studied with positron emission tomography." Annals of Neurology 24(3): 414-419. <http://hdl.handle.net/2027.42/50327>en_US
dc.identifier.issn0364-5134en_US
dc.identifier.issn1531-8249en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/50327
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=3265863&dopt=citationen_US
dc.description.abstractWe compared the severity of motor dysfunction with local cerebral metabolic rates for glucose (lCMRGlc) and the; degree of tissue atrophy in 30 patients with olivopontocerebellar atrophy (OPCA). We devised a scale to quantitate the degree of ataxia in the neurological examinations. lCMRGlc was measured with 18 F-2-fluoro-2-deoxy-D-glucose and positron emission tomography (PET). Tissue atrophy was assessed by visual rating of computed tomographic scans. PET studies revealed Marchked hypometabolism in the cerebellar vermis, cerebellar hemispheres, and brainstem of OPCA patients compared with 30 control subjects. A significant correlation was found between severity of motor impairment and lCMRGlc within the cerebellar vermis, both cerebellar hemispheres, and the brainstem. A significant but weaker relationship was noted between the degree of tissue atrophy in these regions and clinical severity. Partial correlation analysis revealed that motor dysfunction in OPCA correlated more strongly with lCMRGlc than with the amount of tissue atrophy. These results suggest that the clinical manifestations of OPCA are more closely related to the metabolic state of the tissue than to the structural changes in the cerebellum.en_US
dc.format.extent648617 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.titleMotor dysfunction in olivopontocerebellar atrophy is related to cerebral metabolic rate studied with positron emission tomographyen_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 48109en_US
dc.contributor.affiliationumDepartment of Neurology, The University of Michigan, Ann Arbor, MI 48109 ; The University of Michigan, Department of Neurology, 1914/0316 Taubman Health Care Center, 1500 E Medical Center Dr, Ann Arbor, MI 48109-0316en_US
dc.contributor.affiliationumDepartment of Internal Medicine (Division of Nuclear Medicine), The University of Michigan, Ann Arbor, MI 48109en_US
dc.contributor.affiliationumDepartments of Physical Medicine and Rehabilitation, 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.contributor.affiliationumDepartment of adiology, The University of Michigan, Ann Arbor, MI 48109en_US
dc.identifier.pmid3265863en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/50327/1/410240310_ftp.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1002/ana.410240310en_US
dc.identifier.sourceAnnals of Neurologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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