Please use this identifier to cite or link to this item: https://olympias.lib.uoi.gr/jspui/handle/123456789/21434
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dc.contributor.authorGoussia, A. C.en
dc.contributor.authorKyritsis, A. P.en
dc.contributor.authorMitlianga, P.en
dc.contributor.authorBruner, J. M.en
dc.date.accessioned2015-11-24T19:15:00Z-
dc.date.available2015-11-24T19:15:00Z-
dc.identifier.issn0340-5354-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/21434-
dc.rightsDefault Licence-
dc.subjectBrain Neoplasms/*genetics/pathologyen
dc.subjectChromosomes/genetics/ultrastructureen
dc.subjectEpendymoma/*genetics/pathologyen
dc.subjectHumansen
dc.subjectOligodendroglioma/*genetics/pathologyen
dc.titleGenetic abnormalities in oligodendroglial and ependymal tumoursen
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.secondaryhttp://www.ncbi.nlm.nih.gov/pubmed/12013578-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών Υγείας. Τμήμα Ιατρικήςel
heal.publicationDate2001-
heal.abstractOligodendroglial and ependymal tumours are not the most common glial neoplasms; however, they are important subtypes of gliomas with different tumour biologies. Cytogenetic information has suggested that losses of chromosomes 1 p and 19 q are the most frequent genetic alterations in oligodendroglial tumours. Combined loss of these chromosomes has been associated with better chemotherapeutic response and prolonged overall survival. Loss of chromosome 22 is a well defined abnormality in ependymomas. In addition, deletion of chromosome 6 q may be another frequent chromosomic aberration in paediatric ependymomas.en
heal.journalNameJ Neurolen
heal.journalTypepeer-reviewed-
heal.fullTextAvailabilityTRUE-
Appears in Collections:Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά) - ΙΑΤ

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