Dysgerminoma in a child with ataxia-telangiectasia

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dc.contributor.authorKoksal, Yavuz
dc.contributor.authorCaliskan, Umran
dc.contributor.authorUcar, Canan
dc.contributor.authorYurtcu, Muslim
dc.contributor.authorArtac, Hasibe
dc.contributor.authorIlerisoy-Yakut, Zeynep
dc.contributor.authorReisli, Ismail
dc.date.accessioned2020-03-26T17:17:15Z
dc.date.available2020-03-26T17:17:15Z
dc.date.issued2007
dc.departmentSelçuk Üniversitesien_US
dc.description.abstractAlaxia - telangiectasia is an autosomal recessive disease characterized by progressive cerebellar ataxia, oculocutaneous telangiectasia, immunodeficiency, high incidence of cancer; and increased sensitivity to ionizing radiation. The authors report a case of dysgerminoma in a child with high alpha-fetoprotein, CA125 and beta-human chorionic gonadotropin, who has been followed-up for ataxia-letangiectasia for 2 years.en_US
dc.identifier.doi10.1080/08880010701451434en_US
dc.identifier.endpage436en_US
dc.identifier.issn0888-0018en_US
dc.identifier.issue05.08.2020en_US
dc.identifier.pmid17710660en_US
dc.identifier.scopusqualityQ3en_US
dc.identifier.startpage431en_US
dc.identifier.urihttps://dx.doi.org/10.1080/08880010701451434
dc.identifier.urihttps://hdl.handle.net/20.500.12395/21328
dc.identifier.volume24en_US
dc.identifier.wosWOS:000251931700014en_US
dc.identifier.wosqualityQ4en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isoenen_US
dc.publisherTAYLOR & FRANCIS INCen_US
dc.relation.ispartofPEDIATRIC HEMATOLOGY AND ONCOLOGYen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.selcuk20240510_oaigen_US
dc.subjectataxia - telangiectasiaen_US
dc.subjectchildhooden_US
dc.subjectdysgerminomaen_US
dc.subjectCA125en_US
dc.subjectbeta-human chorionic gonadotropinen_US
dc.subjecttreatmenten_US
dc.titleDysgerminoma in a child with ataxia-telangiectasiaen_US
dc.typeArticleen_US

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