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dc.contributor.authorSakorn Pornpraserten_US
dc.contributor.authorChutharat Kasemraden_US
dc.contributor.authorKanyakan Sukunthamalaen_US
dc.date.accessioned2018-09-04T04:42:02Z-
dc.date.available2018-09-04T04:42:02Z-
dc.date.issued2010-10-01en_US
dc.identifier.issn1532432Xen_US
dc.identifier.issn03630269en_US
dc.identifier.other2-s2.0-77956894532en_US
dc.identifier.other10.3109/03630269.2010.513294en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=77956894532&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/50532-
dc.description.abstractHigh performance liquid chromatography (HPLC) on fresh lysates is the standard test for identification of thalassemia. Samples in the form of dried blood spot(s) (DBS) mailed to reference laboratories where HPLC is available could be an alternative. Hemoglobin (Hb) on DBS at day 1, 7, 15 and 30 were analyzed by HPLC and compared to those analyzed from fresh liquid whole blood at day 0. A 100 consistent interpretation of β-thalassemia (β-thal) trait and β-thalHb E disease between liquid whole blood and DBS was observed when analyzing Hb A2 on DBS at a level of 2.79.9 in conjunction with a lower MCV (<80 fL) and MCH (<27 pg) and analyzing β-thalHb E by using Hb E and Hb F at a level of 3048 and >10, respectively. Therefore, our results show that detection of thalassemia carriers using DBS is possible and is the alternative of choice in a low resource setting. © 2010 Informa UK Ltd.en_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectMedicineen_US
dc.titleDiagnosis of thalassemia on dried blood spot samples by high performance liquid chromatographyen_US
dc.typeJournalen_US
article.title.sourcetitleHemoglobinen_US
article.volume34en_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsChiang Mai Neurological Hospitalen_US
Appears in Collections:CMUL: Journal Articles

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