2012, Number 4
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Rev Cubana Hematol Inmunol Hemoter 2012; 28 (4)
Quantitation of hemoglobin A>2 by electrophoresis in agar gel
Miguel-Morales M, Díaz-Barroso LM, Garrote-Santana H, Uley-del Rosario G, Pérez-Diez de los Ríos G, Estrada-del Cueto M
Language: Spanish
References: 12
Page: 423-427
PDF size: 87.79 Kb.
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No abstract.
REFERENCES
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Borgna-Pignatti C, Galanello R. Thalassemias and related disorders: quantitative disorders of hemoglobin synthesis. En: Wintrobe's Clinical Hematology. 12th ed. Philadelphia: Lippincott Williams & Wilkins;2009. p. 1084-1119.
Kaushansky K, Lichtman MA, Beutler E, Kipps TJ, Seligsohn U, Prchal JT. Disorders of globin synthesis: The thalassemias. En: William´s Hematology. 8th ed. New York: McGraw-Hill; 2010.
Perceu L, Satta S, Moi P, Demartis FR, Manunza L, Sollanio MC. KLF1 gene mutations cause borderline Hb A2. Blood. 2011;118(6)4454-8.
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Wajcman H, Preahu C, Bardakdjian-Michau J, Prome D, Riou J, Godart C, et al. Abnormal hemoglobins: laboratory methods. Hemoglobin. 2001 May;25(2):169-81.
Tangvarasittichai S, Tangvarasittichai O, Jermnim N. Comparison of fast protein liquid chromatography (FPLC) with HPLC, electrophoresis & microcolumn chromatography techniques for the diagnosis of ?-thalassaemia. Indian J Med. 2009;129:242-8.
Vrettou C, Kanavakis E, Traeger-Synodinos J, Metaxotou-Mavrommati A, Basiakos I, Maragoudaki E, et al. Molecular studies of thalassemia heterozygotes with raised Hb levels. Hemoglobin. 2000;24:203-20.
Hydragel 15 hemoglobin(E). Ref. 4126. Sebia Hydrasys 2 electrophoresis scanning system. Sebia Company. Evry Cedex. France;2010.
Villegas A. Talasemias: clasificación y diagnóstico. Haematologica/Edición Española. 2010;95(Extra1)23-32.
Bain BJ. Haemoglobinopathy diagnosis: Algorithms, lessons and pitfalls. Blood Rev. 2011;25:205-13.
González R, Ballester JM, Estrada M, Lima F, Martínez G, Wade M, et al. A study of the genetical structure of the Cuban population: red cell and serum biochemical markers. Am J Hum Genet. 1976;28:585-96.