Publication:
Non‐Transferrin Plasma Iron in β‐Thalassaemia/Hb E and Haemoglobin H Diseases

dc.contributor.authorM. Anuwatanakulchaien_US
dc.contributor.authorP. Wasien_US
dc.contributor.authorP. Pootrakulen_US
dc.contributor.authorP. Thuvasethakulen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-10-12T07:44:13Z
dc.date.available2018-10-12T07:44:13Z
dc.date.issued1984-01-01en_US
dc.description.abstractNon‐transferrin plasma iron concentrations were determined in 45 normal controls and in 37 patients with Hb H disease and 104 patients with β‐thalassaemia/Hb E disease. This revealed that non‐transferrin plasma iron exists in cases with severe iron overload, more striking in β‐thalassaemia/Hb E than in Hb H disease. Non‐transferrin plasma iron is associated with higher transferrin iron saturation and higher plasma ferritin levels. The most striking finding was the significantly higher non‐transferrin plasma iron in splenectomized patients with β‐thalassaemia/Hb E disease than in the non‐splenectomized patients. In view of the potential toxicity of non‐transferrin iron, this fraction of iron may be responsible for tissue damage in these patients especially after splenectomy. © Munksgaard 1984en_US
dc.identifier.citationScandinavian Journal of Haematology. Vol.32, No.2 (1984), 153-158en_US
dc.identifier.doi10.1111/j.1600-0609.1984.tb02171.xen_US
dc.identifier.issn16000609en_US
dc.identifier.issn0036553Xen_US
dc.identifier.other2-s2.0-0021368961en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/30705
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0021368961&origin=inwarden_US
dc.subjectMedicineen_US
dc.titleNon‐Transferrin Plasma Iron in β‐Thalassaemia/Hb E and Haemoglobin H Diseasesen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0021368961&origin=inwarden_US

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