The Hb SS disease of Eastern Saudi Arabia has attracted international interest because of its comparatively "benign" course, usually attributed to high levels of Hb F found in these patients. 伪 thalassemia, resulting in hypochromic microcytosis, is also common in this area. We determined the ...
Hb F Hb H Hb M Hb S HBB HBcAb HBcAg HbChesapeake HbCO HBE HBeAb HBeAg HbF HBG HBIG HBLRR HBLV HBME1 HBO HbO2 H-Bomb Sign HBP HBPC HBsAb HBsAg ▼ Complete English Grammar Rules is now available in paperback and eBook formats. ...
The Effect Of Hb F And Alpha-Thalassemia On The Red-Cell Indexes In Sickle-Cell-Anemia. Am J Hematol. 1986;21(4):383-395.Milner PF, Garbutt GJ, Nolan-Davis LV, Jonah F, Wilson LB, Wilson JT: The effect of Hb F and alpha-thalassemiaon the red cell indices in sickle cell anemia...
Erythrocytic anomalies associated with hemoglobin F or hemoglobin H underlie the conditions of thalassemia and methemoglobinemia. The respiratory function of certain anomalous hemoglobins is severely impaired, giving rise to various pathological conditions (for example, anemias). The properties of ...
A combination of 2 forms of thalassemia has been observed in a member of a South Carolina family. The proposita, a 34-year-old black female with hemolytic anemia, had over 50% fetal hemoglobin, an elevated level of hemoglobin A2, and in vitro imbalance in chain synthesis. Family studies ...
We describe hematologic and DNA characterization of thalassemia intermedia in Thai adolescents caused by homozygosity for hemoglobin Malay and compound heterozygosity for hemoglobin Malay/hemoglobin E. A simple DNA assay, based on an allele-specific polymerase chain reaction (PCR), for accurate diagnosis ...
Traeger-Synodinos, J., Harteveld, C.L., Kanavakis, E., Giordano, P., Kattamis, C. & Bernini, L.F. (1999a) Hb Aghia Sophia [a62 (E11) Val.0 (a1)], an `in-frame' deletion causing a-thalassemia. Hemoglobin, 23, 317±324....
In this case, A1c should be measured with other assays not significantly subject to S-β +-thalassemia interference. 展开 关键词: Hemoglobin A1c Hemoglobin S-β +-thalassemia Interference Cation-exchange HPLC DOI: 10.1016/j.cca.2009.08.009 被引量: 15 ...
Molecular studies of beta-thalassemia heterozygotes with raised Hb F levels. Hemoglobin 2000; 24(... C.,Vrettou,E.,... - 《Hemoglobin》 被引量: 0发表: 2000年 Common haplotype dependency of high G gamma-globin gene expression and high Hb F levels in beta-thalassemia and sickle cell ...
Molecular Characterization of α㏕halassemia in Pakistan Common α‐thalassemia (thal) rearrangements were studied in a normal random population and in six ethnic groups of Pakistan. Analyses of 204 individuals f... SN Khan,F Hasan,C Sollaino,... - 《Hemoglobin》 被引量: 4发表: 2009年 Compo...