- A Case of Familial beta-thalassemia Minor
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Kim SH, Han BK, Kim HT, Lee KH, Hwang CH, Cho MK, Choi KR
- KMID: 2208313
- J Korean Pediatr Soc.
- 1995 Apr;38(4):557-560.
Thalassemias are a diverse group of inherited anemias that are characterized by defective synthesis of one or more globin chains. The thalassemias are classified according to the globin chain or... -
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- Comparative analysis of cellulose acetate hemoglobin electrophoresis and high performance liquid chromatography for quantitative determination of hemoglobin A2
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Khosa SM, Usman M, Moinuddin , Mehmood HO, Qamar K
- KMID: 1787912
- Blood Res.
- 2015 Mar;50(1):46-50.
- doi: 10.5045/br.2015.50.1.46
BACKGROUND: The present study is designed to evaluate the reliability and cost effectiveness of cellulose acetate Hb electrophoresis and high performance liquid chromatography (HPLC) in the determination of HbA2 levels. METHODS:... -
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- Clinical Characteristics of Pediatric Thalassemia in Korea: A Single Institute Experience
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Hong CR, Kang HJ, Lee JW, Kim H, Kim NH, Park KD, Park JD, Seong MW, Park SS, Shin HY, Ahn HS
- KMID: 1777663
- J Korean Med Sci.
- 2013 Nov;28(11):1645-1649.
- doi: 10.3346/jkms.2013.28.11.1645
Few literatures have elaborated on the clinical characteristics of children with thalassemia from low-prevalence areas. A retrospective analysis was conducted on children genetically confirmed with thalassemia at Seoul National University... -
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- Comparison of Capillary Electrophoresis with Cellulose Acetate Electrophoresis for the Screening of Hemoglobinopathies
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Kim JE, Kim BR, Woo KS, Kim JM, Park JI, Han JY
- KMID: 1781686
- Korean J Lab Med.
- 2011 Oct;31(4):238-243.
- doi: 10.3343/kjlm.2011.31.4.238
BACKGROUND: beta-thalassemia is primarily found in individuals of Mediterranean and Southeast Asian ancestry. With rapid growth in the Southeast Asian segments of the Korean population, the geographic distribution of hemoglobinopathies... -
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