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Hypophosphatemic osteomalacia demonstrated by Tc-99m MDP bone scan: a case report.

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dc.contributor.authorKim, S-
dc.contributor.authorPark, CH-
dc.contributor.authorChung, YS-
dc.date.accessioned2011-08-17T07:12:52Z-
dc.date.available2011-08-17T07:12:52Z-
dc.date.issued2000-
dc.identifier.issn0363-9762-
dc.identifier.urihttp://repository.ajou.ac.kr/handle/201003/3762-
dc.description.abstractHypophosphatemic osteomalacia, a familial or rarely acquired disorder, is characterized biochemically by hypophosphatemia, decreased renal tubular reabsorption of phosphate, decreased intestinal absorption of calcium, and normal serum calcium. This report concerns a rare case of hypophosphatemic osteomalacia of unknown cause that was shown on Tc-99m MDP bone scanning.-
dc.language.isoen-
dc.subject.MESHAdult-
dc.subject.MESHBone and Bones-
dc.subject.MESHHumans-
dc.subject.MESHHypophosphatemia, Familial-
dc.subject.MESHMale-
dc.subject.MESHOsteomalacia-
dc.subject.MESHTechnetium Tc 99m Medronate-
dc.titleHypophosphatemic osteomalacia demonstrated by Tc-99m MDP bone scan: a case report.-
dc.typeArticle-
dc.identifier.pmid10795690-
dc.identifier.urlhttp://meta.wkhealth.com/pt/pt-core/template-journal/lwwgateway/media/landingpage.htm?issn=0363-9762&volume=25&issue=5&spage=337-
dc.contributor.affiliatedAuthor박, 찬희-
dc.contributor.affiliatedAuthor정, 윤석-
dc.type.localJournal Papers-
dc.citation.titleClinical nuclear medicine-
dc.citation.volume25-
dc.citation.number5-
dc.citation.date2000-
dc.citation.startPage337-
dc.citation.endPage340-
dc.identifier.bibliographicCitationClinical nuclear medicine, 25(5). : 337-340, 2000-
dc.identifier.eissn1536-0229-
dc.relation.journalidJ003639762-
Appears in Collections:
Journal Papers > School of Medicine / Graduate School of Medicine > Nuclear Medicine & Molecular Imaging
Journal Papers > School of Medicine / Graduate School of Medicine > Endocrinology & Metabolism
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