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dc.contributor.authorTasdemir, HA
dc.contributor.authorDagdemir, A
dc.contributor.authorCelenk, C
dc.contributor.authorAlbayrak, D
dc.date.accessioned2020-06-21T15:49:28Z
dc.date.available2020-06-21T15:49:28Z
dc.date.issued2001
dc.identifier.issn0938-7994
dc.identifier.urihttps://doi.org/10.1007/s003300000576
dc.identifier.urihttps://hdl.handle.net/20.500.12712/22239
dc.descriptionWOS: 000166064500023en_US
dc.descriptionPubMed: 11194907en_US
dc.description.abstractOsteopetrosis major (infantile autosomal recessive type) usually presents with pathological fractures, bone marrow failure and some neurological deficits due to remodelling defect of the bone and narrowed bonny channel of the blood supply. Herein we present a case of osteopetrosis major with neurological deficits not attributed to the narrowed carotid channel of the petrous bone, but due to middle cerebral arterial occlusion 2 cm distal to narrowed channel.en_US
dc.language.isoengen_US
dc.publisherSpringer-Verlagen_US
dc.relation.isversionof10.1007/s003300000576en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectosteopetrosisen_US
dc.subjectarteryen_US
dc.subjectocclusionen_US
dc.subjectMRIen_US
dc.subjectCTen_US
dc.titleMiddle cerebral arterial occlusion in a child with osteopetrosis majoren_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume11en_US
dc.identifier.issue1en_US
dc.identifier.startpage145en_US
dc.identifier.endpage147en_US
dc.relation.journalEuropean Radiologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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