A Case Report of Hyperhemolytic Syndrome in Sickle Cell Disease, with a Special Focus on Avoiding the Use of Transfusions

dc.contributor.authorObajed, Al-Ali, Omar
dc.contributor.authorPfliegler, György
dc.contributor.authorMagyari, Ferenc
dc.contributor.authorBorics, Fanni
dc.contributor.authorPinczés, László Imre
dc.contributor.authorIllés, Árpád
dc.contributor.authorBrúgós, Boglárka
dc.date.accessioned2024-04-27T17:02:17Z
dc.date.available2024-04-27T17:02:17Z
dc.date.issued2024
dc.date.oa2024-12-10
dc.date.pasync2024-05-15T23:07:07Z
dc.date.updated2024-04-27T17:02:17Z
dc.description.correctorLB
dc.identifier.citationThalassemia Reports. -14 : 1 (2024), p. 18-25. -Thalass. Rep. - 2039-4357. - 2039-4365
dc.identifier.doihttp://dx.doi.org/10.3390/thalassrep14010003
dc.identifier.issn2039-4357
dc.identifier.issn2039-4365
dc.identifier.opachttps://ebib.lib.unideb.hu/ebib/CorvinaWeb?action=cclfind&resultview=long&ccltext=idno+BIBFORM120764
dc.identifier.urihttps://hdl.handle.net/2437/369352
dc.identifier.urlhttps://www.mdpi.com/2039-4365/14/1/3
dc.identifier.wos001192432200001
dc.languageeng
dc.rights.accessopen access article
dc.rights.ownerszerzők
dc.subject.mabOrvostudományok
dc.subject.mabKlinikai orvostudományok
dc.titleA Case Report of Hyperhemolytic Syndrome in Sickle Cell Disease, with a Special Focus on Avoiding the Use of Transfusions
dc.typefolyóiratcikk
dc.typeesettanulmány
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