thalassemia

Objective To evaluate peripheral blood parameters for diagnostic significance of minor thalassemia.

目的探讨轻型地中海贫血的血液学检测参数变化及临床诊断意义。

Conclusion The increased proportion of immature reticulocytes in thalassemia patients might be one of the main reasons of ineffective erythropoiesis.

结论网织红细胞细胞多参数测定提示，地中海贫血时患者网织红细胞细胞中未成熟细胞所占比例增加可能是导致无效造血的主要原因之一；

Twelve ( 8 males and 4 females) patients with β-thalassemia major received the hematological stem cell transplantation ( HSCT).

12例接受造血干细胞移植治疗的重型β地中海贫血患儿，年龄从25岁～115岁，男8例，女4例。

Analysis and determination on the serum trace element in children with light thalassemia

轻型地中海贫血儿童血清中微量元素含量分析

Objective To determine value of chorionic villus sampling ( CVS ) in early diagnosis of severe thalassemia.

目的探讨绒毛活检在重型地中海贫血早期诊断的应用价值.

Treatment of thalassemia major with unrelated donor bone marrow transplantation

非血缘相关骨髓移植治疗重型地中海贫血的临床研究

Objective To reduce the birthrate of β-thalassemia major and improve the quality of population.

目的为了降低β地中海贫血重症患儿的出生率，达到优生的目的。

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

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

Objective To reduce the birth rate of β-thalassemia major and improve the quality of population.

目的减少β-地中海贫血重症患儿的出生。

Effect of Pingyangmycin on partial splenic artery embolization in infant thalassemia

平阳霉素用于婴幼儿地中海贫血部分性脾动脉栓塞术的疗效

Genetic Study on 27 Children with β-thalassemia Major and Their Parents in Sichuan Area

四川地区重型β-地中海贫血患儿及双亲基因突变的研究

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

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

A pair of twin girls suffered from thalassemia major.

一对孪生姐妹婴儿患上了重型地中海贫血。

Use of Synthetic Oligonucleotides in the Detection of β-thalassemia Mutation in Chinese

用合成的寡核苷酸探针鉴定中国人β-地中海贫血基因突变

Genetic and Clinical Features of Children with β-Thalassemia Intermedia

中间型β珠蛋白生成障碍贫血患儿基因型及临床特点

Prophylaxis of Transplantation-related Complications after Allogeneic Stem Cell Transplantation in β-thalassemia Major

儿童重型β-地中海贫血异基因造血干细胞移植后并发症的防治

Umbilical cord blood transplantation for patients with β-thalassemia major

脐血移植治疗重型β地中海贫血的临床研究

Conclusion The results showed that Allo PBSCT was successful in treating β thalassemia major.

结论异基因外周血造血干细胞移植治疗重型β地贫患儿已获得成功。

Objective To investigate the safety and accuracy of diagnosing alpha-thalassemia with extraembryonic coelomic cells.

目的探讨胚外体腔穿刺液应用于α地中海贫血产前诊断的安全性及准确性。

Conclusion Extraembryonic coelomic cells can be used in the early prenatal diagnosis of alpha-thalassemia by PCR technique. But the sensitivity of this technique should be increased.

结论通过胚外体腔穿刺术取胚外体腔细胞行PCR检测可用于α地中海贫血的早期产前诊断，但应进一步提高诊断方法的敏感性。

Study on gene distribution and blood routine test parameter variation in β-thalassemia patients

β-地中海贫血的基因分布及其血常规参数变异分析

A prenatal diagnosis of β thalassemia was carried out in South China using a in vitro DNA amplification by a polymerase chain reaction and isotope-labeled or nonradioactive probes.

应用聚合酶链式反应体外DNA放大和同位素或非同位素标记的探针在我国南方进行了β地中海贫血的产前诊断。

Knowledge and attitudes of medical counselors and Thalassemia prevention and control in Bose

百色市医务人员的遗传咨询态度与地中海贫血预防

Conclusions It suggests that the PCR-RDB assay is effective in preventing the birth of β-thalassemia major and has clinical significance in improving the population quality.

结论PCR-RDB技术可有效减少β地中海贫血重症患儿的出生，具有重要的优生学意义。

Transplantation with Combination of Umbilical Cord Blood and Neonatal Peripheral Blood in the Treatment of A Patient with β-thalassemia Major

脐带血、新生儿外周血混合移植治疗1例重型β-地中海贫血

The Thalassemia Survey of Li Nationality in Hainan Island, China

海南岛黎族人群的地中海贫血病调查报告

Methods The chest radiographs and CT findings in two cases of intrathoracic tumor-simulating EMH with thalassemia were analyzed respectively and some related literatures were reviewed.

方法回顾性分析2例地中海贫血患者的胸部瘤样髓外造血组织平片和CT表现。

Change of Serum Ferritin Level in Hyper Transfusion Thalassemia Major Children Treated by Different Dosage of Iron Chelator

不同剂量铁螯合剂治疗高量输血重型β珠蛋白生成障碍贫血患儿血清铁蛋白的变化

Objective To establish an automatic, high throughput, quick detection method of α-thalassemia.

目的建立自动化、高通量、准确快速检测缺失型α-地中海贫血基因型的技术。

Prenatal diagnosis was carried out by the mentioned techniques above for fetuses who were in the risk of thalassemia major. 5.

将上述方法运用于重型地中海贫血高风险胎儿的产前诊断中。