Gliofibroma

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dc.authoridAYDIN, Nasuhi/0000-0003-3145-2432
dc.authorwosidAydin, Nasuhi E/B-6536-2012
dc.authorwosidAYDIN, Nasuhi Engin/L-1607-2019
dc.authorwosidAYDIN, Nasuhi/O-9043-2016
dc.contributor.authorErguvan-Önal, R
dc.contributor.authorAtes, O
dc.contributor.authorÖnal, C
dc.contributor.authorAydin, NE
dc.contributor.authorKoçak, A
dc.date.accessioned2024-08-04T20:14:48Z
dc.date.available2024-08-04T20:14:48Z
dc.date.issued2004
dc.departmentİnönü Üniversitesien_US
dc.description.abstractAlthough gliofibroma is a rare and incompletely characterized tumor, recent publications have revealed new aspects of this entity. The case of a 16-year-old boy who was diagnosed as having a gliofibroma is presented here, and the problems regarding nosology are discussed in the light of the recent literature.en_US
dc.identifier.doi10.1177/030089160409000133
dc.identifier.endpage160en_US
dc.identifier.issn0300-8916
dc.identifier.issn2038-2529
dc.identifier.issue1en_US
dc.identifier.pmid15143993en_US
dc.identifier.scopus2-s2.0-2142640303en_US
dc.identifier.scopusqualityQ3en_US
dc.identifier.startpage157en_US
dc.identifier.urihttps://doi.org/10.1177/030089160409000133
dc.identifier.urihttps://hdl.handle.net/11616/93985
dc.identifier.volume90en_US
dc.identifier.wosWOS:000221284500032en_US
dc.identifier.wosqualityN/Aen_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isoenen_US
dc.publisherSage Publications Ltden_US
dc.relation.ispartofTumori Journalen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectbrainen_US
dc.subjectdesmoplastic tumoren_US
dc.subjectgliofibromaen_US
dc.titleGliofibromaen_US
dc.typeArticleen_US

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