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dc.contributor.authorOjo, J O-
dc.contributor.authorOluwole, A F-
dc.contributor.authorOsoniyi, R O-
dc.contributor.authorDurosinmi, M A-
dc.contributor.authorAboderin, A O-
dc.date.accessioned2024-08-27T11:41:19Z-
dc.date.available2024-08-27T11:41:19Z-
dc.date.issued2006-06-
dc.identifier.citationAfr. J. Med. Med. Sci. (2006) 35(4) : 461-467en_US
dc.identifier.issn1116-4077-
dc.identifier.urihttp://adhlui.com.ui.edu.ng/jspui/handle/123456789/2806-
dc.descriptionArticleen_US
dc.description.abstractThe clinical application of trace elements in the management of Sickle Cell Anaemia (SCA) has not become standard recommended practice despite decade s of research. A major reason for this is the ambivalence in published results as to the relative importance of some of these elements in the disease. An attempt has been mad e in this work to correct some of the various factors that could contribute to such inconsistencies. Results from separate investigations carried out on Nigerian subjects by our group, using both INA A and PIX E method s have been holistically evaluated and compared. Trace and minor elements were determined in wholeblood, erythrocytes, plasma, headhair and nail obtained from S C A patients in steady state and compare d with identical sample s from normal controls. Twelve elements were determined in blood while 2 0 and 3 0 elements were analysed in nail and hair sample s respectively from the total 2 2 5 subjects. T h e results indicate a general mild zinc deficiency, more serious f or males, in Nigeria n S C A patients. It is clear that the elements N a, K, Rb and Br play key role s in maintaining homeostasis in the steady-state S C A patients. Possible sender influence in the utilization of K, Br and F e in S C A is also suggested .en_US
dc.description.sponsorshipCOLLEGE OF MEDICINEen_US
dc.language.isoenen_US
dc.publisherCOLLEGE OF MEDICINEen_US
dc.subjectINAAen_US
dc.subjectsickle cell anaemiaen_US
dc.subjecttrace elementsen_US
dc.subjectPIXEen_US
dc.titleDetermination of trace elements status of Nigerians with sickle cell anaemia using INAA and PIXEen_US
dc.typeArticleen_US
Appears in Collections:African Journal of Medicine and Medical Sciences

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