Please use this identifier to cite or link to this item: http://dl.umsu.ac.ir/handle/Hannan/178633
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dc.contributor.authorGait-carr, Eleanoren_US
dc.contributor.authorConnolly, Daniel J Aen_US
dc.contributor.authorKing, Daviden_US
dc.date.accessioned2013en_US
dc.date.accessioned2017-07-04T11:51:55Z-
dc.date.available2017-07-04T11:51:55Z-
dc.date.issued2017en_US
dc.identifier.issnen_US
dc.identifier.otheren_US
dc.identifier.urien_US
dc.identifier.urihttp://dl.umsu.ac.ir/handle/Hannan/178633-
dc.description.abstracten_US
dc.format.extentVOLUME:39en_US
dc.format.extentISSUE:3en_US
dc.format.extentSTARTPAGE:233en_US
dc.format.extentENDPAGES:234en_US
dc.publisheren_US
dc.relation.haspartJPHO 2017 Volume 39 Issue 3 April (14).pdfen_US
dc.subjectMedical Scienceen_US
dc.subject233en_US
dc.subject234en_US
dc.subjectMedical Scienceen_US
dc.subjectChildrenen_US
dc.subjectdisorder characterized by slowlyen_US
dc.subjecthereditary spherocytosisen_US
dc.subjectidiopathic cerebrovascularen_US
dc.subjectOncologyen_US
dc.subjectmoyamoyaen_US
dc.subjectoyamoya disease is anen_US
dc.subjectprogressive steno-en_US
dc.subjectStrokeen_US
dc.titleMoyamoya Syndrome Associated With Hereditary Spherocytosis : An Emerging Clinical Entityen_US
dc.typeArticleen_US
dc.journal.monthAprilen_US
dc.journal.issueIssue 3en_US
dc.journal.volumeVolume 39en_US
dc.journal.titleMoyamoya Syndrome Associated With Hereditary Spherocytosis : An Emerging Clinical Entityen_US
dc.subscribeUMSUen_US
Appears in Collections:Journal of pediatric hematology oncology 2017

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