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Acromegaly
dc.contributor.authorBarkan, Ariel L.en_US
dc.date.accessioned2006-04-10T15:08:05Z
dc.date.available2006-04-10T15:08:05Z
dc.date.issued1992-08en_US
dc.identifier.citationBarkan, Ariel L. (1992/08)."Acromegaly." Trends in Endocrinology and Metabolism 3(6): 205-210. <http://hdl.handle.net/2027.42/29921>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6T3K-4C1X563-38/2/fae1c09cd3ee30982aef4f40e03fac8ben_US
dc.identifier.urihttps://hdl.handle.net/2027.42/29921
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=18407101&dopt=citationen_US
dc.description.abstractIn the majority of cases, acromegaly is due to GH hypersecretion by a somatotroph pituitary tumor. The etiology of acromegaly is not known, and may be related to GHRH hypersecretion, intrinsic pituitary defect, or a combination thereof. Recent physiologic data and molecular biology techniques provide insights into the pathophysiology of this condition. Treatment options include surgery, radiation, and judicious administration of pharmacologic compounds inhibiting GH secretion and tumor growth.en_US
dc.format.extent1001615 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleAcromegalyen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelInternal Medicine and Specialtiesen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDivision of Endocrinology and Metabolism, University of Michigan Medical Center, Ann Arbor, MI 48109-0354, USAen_US
dc.identifier.pmid18407101en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/29921/1/0000278.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/1043-2760(92)90029-Zen_US
dc.identifier.sourceTrends in Endocrinology and Metabolismen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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