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dc.contributor.authorGueven, Ayla
dc.contributor.authorOezgen, Tolga
dc.contributor.authorBelet, Uemit
dc.contributor.authorAydin, Murat
dc.date.accessioned2020-06-21T15:19:21Z
dc.date.available2020-06-21T15:19:21Z
dc.date.issued2007
dc.identifier.issn0334-018X
dc.identifier.urihttps://hdl.handle.net/20.500.12712/19855
dc.descriptionAYDIN, MURAT/0000-0001-7374-229X; GUVEN, AYLA/0000-0002-2026-1326; Ozgen, Ilker Tolga/0000-0001-6592-9652en_US
dc.descriptionWOS: 000249747100010en_US
dc.descriptionPubMed: 17937067en_US
dc.description.abstractThe diagnosis of acromegaly requires a glucose-suppressed growth hormone (GH) nadir greater than 1 mu g/l associated with clinical symptoms and signs. Here, we present a patient who has acromegalic clinical findings associated with a nadir GH level < 1 mu g/l during an oral glucose tolerance test.en_US
dc.language.isoengen_US
dc.publisherFreund Publishing House Ltden_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectacromegalyen_US
dc.subjectgrowth hormoneen_US
dc.subjectoral glucose tolerance testen_US
dc.subjectinferior petrosal sinus sampleen_US
dc.titleAcromegaly symptoms without pituitary adenoma in an adolescenten_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume20en_US
dc.identifier.issue8en_US
dc.identifier.startpage945en_US
dc.identifier.endpage949en_US
dc.relation.journalJournal of Pediatric Endocrinology & Metabolismen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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