1.
Immunologic function of children with severe mediterranean anemia after partial splenic embolization
大部脾栓塞术对重型地中海贫血患儿免疫功能影响的研究
2.
Allogeneic Hematopoietic Stem Cell Transplantation for Pesaro Class 3 Thalassemia Major Using Fludarabine-based Conditioning Regimen;
“氟达拉宾”为主预处理HSCT治疗PesaroⅢ级重型地中海贫血
3.
Meta-Analysis of the Efficacy and Safety of Combined Chelation Therapy in Patients with Thalassemia Major
去铁酮联合去铁胺治疗重型地中海贫血铁超负荷临床疗效及安全性的Meta分析
4.
Single-Cell Raman Spectroscopy of Erythrocytes from Hemoglobin Bart′s Hydrops
重型α地中海贫血红细胞的拉曼光谱
5.
Unrelated bone marrow transplantation for β-thalassemia major:report of the first2successful cases in Asia
非血缘供者骨髓移植成功治疗重型β地中海贫血亚洲首报2例
6.
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
7.
Haploidentical hematopoietic stem cell transplantation for beta-thalassemia major in children
单倍体造血干细胞移植治疗儿童重型β-地中海贫血
8.
Effect of siRNA on the Alpha-Globin of Major Beta-Thalassemia Erythroid Cells Cultured in Vitro;
siRNA对体外培养重型β地中海贫血红系细胞α-珠蛋白的调控作用
9.
MR imaging of liver iron storage in patients with β-thalassaemia major:correlation analysis with pathology
重型β地中海贫血肝脏铁沉积的MRI与病理学相关分析
10.
Analysis of Paramenters of Red Blood Cell in the Screening of β-Thalassaemia Minor
轻型β-地中海贫血的红细胞参数分析
11.
Phenotypic Analysis of Silent α-Thalassemia the Young Popultion
育龄青年静止型α-地中海贫血的表型分析
12.
Genotypes of β Thalassemia in Guangxi
广西地区β地中海贫血基因突变类型分析
13.
Relationship between cellular immune function during conditioning and graft rejection in patients with beta-thalassemia major
重型β地中海贫血造血干细胞移植排斥与受者细胞免疫功能的关系
14.
Combined transplantation of bone marrow and umbilical cord blood of same sibling in eight children with beta-thalassemia major
动员后的同胞骨髓联合脐血混合移植治疗儿童重型β-地中海贫血8例
15.
The sensitiveness of light-duty Mediterranean anaemia is 93. 2% , peculiar is 94. 1%;
轻型地中海贫血的敏感性为93.2%、特异性为94.1%;
16.
Rapid Diagnosis of Nondeletion α-thalassemia by Reverse Dot Blot;
反向点杂交快速诊断非缺失型α-地中海贫血
17.
Identification of a Novel Silent β Thalassemia Gene;
一种新的静止型β地中海贫血基因的鉴定
18.
Prenatal diagnosis of a case at-risk for compound heterozygotes of SEA HPFH deletion and β-thalassemia in a Chinese family.
缺失型β-地中海贫血一个家系的产前诊断