珠蛋白生成障碍性贫血

去铁酮和去铁胺治疗珠蛋白生成障碍性贫血临床疗效及安全性的Meta分析

Meta-analysis of the efficacy and safety of combined therapy with deferiprone and deferoxamine in thalassemia major patients

目的探讨葡萄糖-6磷酸脱氢酶（G-6PD）活性对珠蛋白生成障碍性贫血（地贫）的辅助诊断价值及其适用范围。

Objective : To approach the value and applicability of the activity of Glucose-6-phosphate dehydrogenase ( G6PD ) for the auxiliary diagnosis of thalassemia .

目的观察去铁胺（DF）对重度珠蛋白生成障碍性贫血（β地中海贫血，β地贫）患儿长期采用输血治疗后铁负荷过多的驱铁作用。

Objective To evaluate the effect of the intermittent deferomamine ( DF ) therapy on relieving iron overload caused by transfusion in children with β thalassemia .

测定116例珠蛋白生成障碍性贫血、37例缺铁性贫血患者及45例正常人的FEP水平。

Free erythrocyte Protoporphyrin ( FEP ) were determined in 116 thalassemia patients , 37 iron deficiency anemia patients and 45 normal subjects .

珠蛋白生成障碍性贫血妊娠妇女血清转铁蛋白受体的测定

Detection of soluble serum transferrin receptor of thalassemia women during pregnancy

药物基因调控治疗β珠蛋白生成障碍性贫血研究进展

Advances of Gene Regulation with Agents Treatment of β Thalassemia

珠蛋白生成障碍性贫血患者红细胞游离原卟啉水平的研究

A study of free erythrocyte protoporphyrin in thalassemia

造血干细胞移植治疗珠蛋白生成障碍性贫血的若干经验

Experiences of Haematopoietic Stem Cell Transplantation on Thalassemia

珠蛋白生成障碍性贫血网织红细胞的分群分析网织红细胞参数在肾移植受者中的临床应用

A clustering analysis of reticulocyte in thalassemia Utility of reticulocyte parameters in diagnosis of anemia

珠蛋白生成障碍性贫血的铁螯合剂治疗

Thalassemia Treated by Iron Chelator in Children

重型β珠蛋白生成障碍性贫血肝脏病理与相关因素的多重回归分析

Multiple Regression Analysis of Liver Pathology and Other Factors in Children with β Thalassemia Major

无脑白质影像学改变的晚发婴儿型异染性脑白质营养不良重型珠蛋白生成障碍性贫血患儿基因突变及免疫紊乱的特点

Late-onset infantile metachromatic leukodystrophy without MRI abnormalities in white matter Study on Genotypes of Children with Beta-Thalassemia Major and Their Immune Abnormalities

运用单管多重聚合酶链反应检测海南黎族人群中三种缺失型α-珠蛋白生成障碍性贫血基因

Detection of deletional determinants of α - thalassemia in Li people in Hainan Province by a single tube multiplex polymerase chain reaction method

获得性纯红再障患者γδT细胞亚群和功能的研究珠蛋白生成障碍性贫血网织红细胞的分群分析

Analysis of Peripheral Blood γδ T Cell Subsets and Functions in Patients with Pure Red Cell Aplastic Anemia ; A clustering analysis of reticulocyte in thalassemia

目的对临床诊断为轻型β-珠蛋白生成障碍性贫血患者进行β-珠蛋白基因单核苷酸多态性分析。羟基脲治疗重型β地中海贫血

Objective To investigate the single nucleotide polymorphisms ( SNP ) of beta-globin gene in beta-thalassaemia carrier . Clinical study of hydroxyurea for the treatment of severe beta - thalassaemia