6.陈文强,等. 广西地区β-地中海贫血复合异常血红蛋白E的基因型与表现型的研究。 7. Nancy F. Olivieri*,et al. Hb E/beta-thalassaemia: a common & clinically diverse disorder 8.Thongperm Munkongdee,et al. Predictive SNPs for β0thalassemia/HbE disease severity...
2012. Hemoglobin E/beta thalassemia the second most common cause of transfusion dependent beta thalassemia in the Gwalior-Chambal region of central India. Hemoglobin 36:485-490.Kumar R, Sharma D C, Kishor P. "Hb E/β-Thalassemia: The Second Most Common Cause of Transfusion-Dependent ...
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 ...
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Beta-thalassemia intermediate patients show a remarkable clinical heterogeneity. We examined the phenotypic diversity of 950 beta-thalassemia/Hb E patients... O Sripichai,W Makarasara,T Munkongdee,... - 《American Journal of Hematology》 被引量: 151发表: 2008年 加载更多来源...
(2008) A scoring system for the classification of beta-thalassemia/Hb E disease severity. Am J Hematol 83: 482–484. [18] Chong SS, Boehm CD, Cutting GR, Higgs DR (2000) Simplified multiplex-PCR diagnosis of common southeast asian deletional determinants of alpha-thalassemia. Clin Chem 46...
More than 60 different thalassemia syndromes resulting from the interactions of these heterogeneous alleles have been observed. The majority of patients in the hospital based-study are compound heterozygotes for beta thalassemia alleles and another hemoglobinopathy namely Hb E, highly prevalent in Thailand...
[4] Sreedharanunni S, Chhabra S, Hira JK, Bansal D, Sharma P, Das R. β-Thalassemia Intermedia Caused by Compound Heterozygosity for Hb Lepore-Hollandia and β-Thalassemia is Rare in the Indian Population. Hemoglobin. 2015;39(5):362-365. doi:10.3109/03630269.2015.1064004 ...
Delineation of the molecular basis of delta- and normal HbA2 beta-thalassemia. In this study, we used cloning and sequence analysis to define the molecular defect in two delta-thalassemia genes, one associated with reduced output of d... P Moi,E Paglietti,A Sanna,... - 《Blood》 被引量...
Mitochondrial changes in [beta].sup.0-thalassemia/Hb E disease Clinical assessment, hematological studies and molecular analyses were performed in 102 pediatric patients with Hb H disease in northern Thailand. A total ... K Khungwanmaythawee,W Sornjai,A Paemanee,... 被引量: 1发表: 2016年 加...