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dc.contributor.authorCeyhan, Meltem
dc.contributor.authorCelik, Fatma Cakmak
dc.contributor.authorElmali, Muzaffer
dc.contributor.authorGurmen, Nevzat
dc.date.accessioned2020-06-21T14:47:28Z
dc.date.available2020-06-21T14:47:28Z
dc.date.issued2010
dc.identifier.issn1895-1058
dc.identifier.urihttps://doi.org/10.2478/s11536-009-0062-1
dc.identifier.urihttps://hdl.handle.net/20.500.12712/17797
dc.descriptionWOS: 000278178900016en_US
dc.description.abstractGaucher's disease is an inherited storage disease caused by a deficiency of the enzyme glucocerebrosidase. Although the hepatic manifestations are seen frequently, pulmonary and cardiovascular involvements are known to be very rare in Gaucher's disease. This report presents these rare findings made by conventional radiography, computerized tomography (CT), and High-resolution CT (HRCT) of a 16-year-old female patient with fatal Gaucher's disease.en_US
dc.language.isoengen_US
dc.publisherVersitaen_US
dc.relation.isversionof10.2478/s11536-009-0062-1en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectGaucher's diseaseen_US
dc.subjectCardiovascular calcificationen_US
dc.subjectPulmonary interstitial involvementen_US
dc.titleAn unusual form of Gaucher's disease: pulmonary and cardiovascular involvement and cholelitiasisen_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume5en_US
dc.identifier.issue4en_US
dc.identifier.startpage495en_US
dc.identifier.endpage498en_US
dc.relation.journalCentral European Journal of Medicineen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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