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dc.contributor.authorElli, Murat
dc.contributor.authorAydin, Oguz
dc.contributor.authorPinarli, Faruk Guclu
dc.contributor.authorDagdemir, Ayhan
dc.contributor.authorDabak, Nevzat
dc.contributor.authorSelcuk, Mustafa Bekir
dc.contributor.authorAcar, Sabri
dc.date.accessioned2020-06-21T15:25:31Z
dc.date.available2020-06-21T15:25:31Z
dc.date.issued2006
dc.identifier.issn0888-0018
dc.identifier.urihttps://doi.org/10.1080/08880010600812561
dc.identifier.urihttps://hdl.handle.net/20.500.12712/20413
dc.descriptionPinarli, Faruk Guclu/0000-0002-3241-2478en_US
dc.descriptionWOS: 000239966800007en_US
dc.descriptionPubMed: 16928653en_US
dc.description.abstractMelanotic neuroectodermal tumor of infancy (MNTI) is a rare neoplasm that often occurs during the first year of life. More than 90% of MNTIs occur in the head and neck region, with most on the anterior part of the maxillary ridge. MNTI has also been reported in the mediastinum, thigh, foot, shoulder, and gonads. Here the authors report a rare case of MNTI of the femur in a 3-month-old child.en_US
dc.language.isoengen_US
dc.publisherTaylor & Francis Incen_US
dc.relation.isversionof10.1080/08880010600812561en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectmelanotic neuroectodermal tumor of infancyen_US
dc.subjectboneen_US
dc.subjectfemuren_US
dc.titleMelanotic neuroectodermal tumor of infancy of the femuren_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume23en_US
dc.identifier.issue7en_US
dc.identifier.startpage579en_US
dc.identifier.endpage586en_US
dc.relation.journalPediatric Hematology and Oncologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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