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dc.contributor.authorKelleher, T*
dc.contributor.authorAquilina, K*
dc.contributor.authorKeohane, C*
dc.contributor.authorO'Sullivan, M G*
dc.date.accessioned2012-02-03T15:05:58Z
dc.date.available2012-02-03T15:05:58Z
dc.date.issued2012-02-03T15:05:58Z
dc.identifier.citationBr J Neurosurg. 2005 Aug;19(4):345-8.en_GB
dc.identifier.issn0268-8697 (Print)en_GB
dc.identifier.issn0268-8697 (Linking)en_GB
dc.identifier.pmid16455542en_GB
dc.identifier.doi10.1080/02688690500305464en_GB
dc.identifier.urihttp://hdl.handle.net/10147/208869
dc.description.abstractIntramedullary capillary haemangioma is extremely rare and only four cases have been previously reported. We describe a further case, outlining the clinical, radiological, surgical and pathological features.
dc.language.isoengen_GB
dc.subject.meshHemangioma, Capillary/*diagnosis/pathology/surgeryen_GB
dc.subject.meshHumansen_GB
dc.subject.meshMagnetic Resonance Imagingen_GB
dc.subject.meshMaleen_GB
dc.subject.meshMiddle Ageden_GB
dc.subject.meshSpinal Cord Neoplasms/*diagnosis/pathology/surgeryen_GB
dc.subject.meshThoracic Vertebraeen_GB
dc.titleIntramedullary capillary haemangioma.en_GB
dc.contributor.departmentDepartment of Neurosurgery, Cork University Hospital, Wilton, Cork, Ireland.en_GB
dc.identifier.journalBritish journal of neurosurgeryen_GB
dc.description.provinceMunster
html.description.abstractIntramedullary capillary haemangioma is extremely rare and only four cases have been previously reported. We describe a further case, outlining the clinical, radiological, surgical and pathological features.


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