Severe Hemolytic Anaemia due to Pyruvate Kinase Deficiency in a Patient With Coexistent ?-Thalassaemia Trait: A Case Report

dc.contributor.authorBelgemen-Ozer, Tugba
dc.date.accessioned2025-11-16T19:34:14Z
dc.date.issued2025
dc.departmentİstanbul Medeniyet Üniversitesi
dc.description.abstract[Abstract Not Available]
dc.identifier.doi10.1111/jpc.70174
dc.identifier.endpage1685
dc.identifier.issn1034-4810
dc.identifier.issn1440-1754
dc.identifier.issue10
dc.identifier.pmid40817439
dc.identifier.scopus2-s2.0-105013114970
dc.identifier.scopusqualityQ2
dc.identifier.startpage1681
dc.identifier.urihttps://doi.org/10.1111/jpc.70174
dc.identifier.urihttps://hdl.handle.net/20.500.14730/15287
dc.identifier.volume61
dc.identifier.wosWOS:001551668100001
dc.identifier.wosqualityN/A
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherWiley
dc.relation.ispartofJournal of Paediatrics And Child Health
dc.relation.publicationcategoryDiğer
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WOS_20250302
dc.subjectcase report
dc.subjectheterozygous beta-thalassaemia
dc.subjecthomozygous pyruvate kinase deficiency
dc.subjectmicrocytic anaemia
dc.subjectnon-spherocytic hemolytic anaemia
dc.titleSevere Hemolytic Anaemia due to Pyruvate Kinase Deficiency in a Patient With Coexistent ?-Thalassaemia Trait: A Case Report
dc.typeEditorial

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