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The North American Multiple System Atrophy Study Group

dc.contributor.authorGilman, Siden_US
dc.contributor.authorTrojanowski, John Q.en_US
dc.contributor.authorOzelius, Laurie J.en_US
dc.contributor.authorShults, Clifford W.en_US
dc.contributor.authorLow, Phillip A.en_US
dc.contributor.authorForoud, Tatianaen_US
dc.contributor.authorMasliah, E.en_US
dc.contributor.authorSandroni, Paolaen_US
dc.contributor.authorLee, Virginia M-Y.en_US
dc.contributor.authorTanner, Caroline M.en_US
dc.contributor.authorKukull, W.en_US
dc.contributor.authorMay, S. J.en_US
dc.date.accessioned2006-09-08T19:29:32Z
dc.date.available2006-09-08T19:29:32Z
dc.date.issued2005-12en_US
dc.identifier.citationGilman, S.; May, S. J.; Shults, C. W.; Tanner, C. M.; Kukull, W.; Lee, V. M.-Y.; Masliah, E.; Low, P.; Sandroni, P.; Trojanowski, J. Q.; Ozelius, L.; Foroud, T.; (2005). "The North American Multiple System Atrophy Study Group." Journal of Neural Transmission 112(12): 1687-1694. <http://hdl.handle.net/2027.42/41653>en_US
dc.identifier.issn1435-1463en_US
dc.identifier.issn0300-9564en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/41653
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=16284910&dopt=citationen_US
dc.description.abstractThe North American Multiple System Atrophy Study Group involves investigators in 12 US medical centers funded by a grant from the National Institutes of Health. The objectives are to examine the environmental and genetic risk factors for MSA; elucidate pathogenic mechanisms underlying the disorder; and refine evaluations used for assessment. During its first year, the group enrolled 87 patients, implemented four cores, and initiated four scientific projects. Most patients among the 87 had parkinsonian features, which frequently began asymmetrically and remained asymmetrical; one-third responded to levodopa and many developed levodopa complications; almost two-thirds of the patients had cerebellar dysfunction, of these 90% had ataxia; urinary incontinence occurred commonly, and sleep disorders affected most. The investigators studied the effects of oxidative and nitrative stress upon the formation of alpha-synuclein inclusions; generated transgenic models of alpha-synuclein accumulation that recapitulate several behavioral and neuropathological features of MSA; and compared the severity of the autonomic features of MSA, Parkinson’s disease and dementia with Lewy bodies.en_US
dc.format.extent64157 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherSpringer-Verlag; Springer-Verlag/Wienen_US
dc.subject.otherMedicine & Public Healthen_US
dc.subject.otherPsychiatryen_US
dc.subject.otherNeurologyen_US
dc.subject.otherPharmacology/Toxicologyen_US
dc.subject.otherKeywords: Multiple System Atrophy, Parkinsonism, Cerebellar Ataxia, Autonomic Failure.en_US
dc.titleThe North American Multiple System Atrophy Study Groupen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelPublic Healthen_US
dc.subject.hlbsecondlevelPsychologyen_US
dc.subject.hlbsecondlevelNeurosciencesen_US
dc.subject.hlbsecondlevelMolecular, Cellular and Developmental Biologyen_US
dc.subject.hlbtoplevelSocial Sciencesen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Neurology, , University of Michigan, Ann Arbor, MI, USA,en_US
dc.contributor.affiliationotherDepartment of Pathology & Laboratory Medicine, Center on Neurological Disease Research, , University of Pennsylvania, Philadelphia, PA, USA,en_US
dc.contributor.affiliationotherDepartment of Neurology, , Mayo Clinic, Rochester, MA, USA,en_US
dc.contributor.affiliationotherDepartment of Epidemiology, , University of Washington, Seattle, WA, USA,en_US
dc.contributor.affiliationotherDepartment of Molecular Genetics, , Albert Einstein College of Medicine, Bronx, NY, USA,en_US
dc.contributor.affiliationotherDepartment of Medicine and Molecular Genetics, , Indiana University School of Medicine, Indianapolis, IN, USA,en_US
dc.contributor.affiliationotherDepartment of Pathology & Laboratory Medicine, Center on Neurological Disease Research, , University of Pennsylvania, Philadelphia, PA, USA,en_US
dc.contributor.affiliationotherVA San Diego Healthcare System, San Diego, CA, USA, ; Department of Neurosciences, , University of California, San Diego, La Jolla, CA, USA,en_US
dc.contributor.affiliationotherDepartment of Family & Preventive Medicine, , University of California San Diego, La Jolla, CA, USA, ; Department of Neurosciences, , University of California, San Diego, La Jolla, CA, USA,en_US
dc.contributor.affiliationotherDepartment of Neurology, , Mayo Clinic, Rochester, MA, USA,en_US
dc.contributor.affiliationotherDepartment of Clinical Research, , Parkinson’s Institute, Sunnyvale, CA, USA,en_US
dc.contributor.affiliationotherDepartment of Neurosciences, , University of California, San Diego, La Jolla, CA, USA,en_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.identifier.pmid16284910en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/41653/1/702_2005_Article_381.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1007/s00702-005-0381-6en_US
dc.identifier.sourceJournal of Neural Transmissionen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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