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Idiopathic isolated laryngotracheobronchial cartilage calcification in a child

dc.contributor.authorCeyhan, Meltem
dc.contributor.authorNural, Mehmet Selim
dc.contributor.authorElmali, Muzaffer
dc.contributor.authorBayrak, Kay Koray
dc.date.accessioned2020-06-21T15:17:59Z
dc.date.available2020-06-21T15:17:59Z
dc.date.issued2008
dc.identifier.issn0899-7071
dc.identifier.issn1873-4499
dc.identifier.urihttps://doi.org/10.1016/j.clinimag.2007.04.026
dc.identifier.urihttps://hdl.handle.net/20.500.12712/19528
dc.descriptionWOS: 000252295000011en_US
dc.descriptionPubMed: 18164396en_US
dc.description.abstractLaryngeal, tracheal, and bronchial cartilage calcification is quite rare in children. It was reported to occur in congenital cardiovascular diseases, Keutel syndrome, chondroplasia punctata, warfarin embryopathy, and warfarin sodium therapy. It can occur idiopathically as well. Laryngotracheobronchial cartilage calcification is demonstrated in this report by chest radiography and multiplanar three-dimensional CT examination in a 2.5-year-old boy with nonspecific cough. (C) 2008 Elsevier Inc. All rights reserved.en_US
dc.language.isoengen_US
dc.publisherElsevier Science Incen_US
dc.relation.isversionof10.1016/j.clinimag.2007.04.026en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectlaryngotracheobronchial cartilage calcificationen_US
dc.subjectcomputed tomographyen_US
dc.subjectchest radiographyen_US
dc.subjectchilden_US
dc.titleIdiopathic isolated laryngotracheobronchial cartilage calcification in a childen_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume32en_US
dc.identifier.issue1en_US
dc.identifier.startpage51en_US
dc.identifier.endpage53en_US
dc.relation.journalClinical Imagingen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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