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。
OBJECTIVE: To study the status of iron metabolism and erythropoietic proliferation in children with various genotypes of thalassemia. 目的:探讨不同基因型地中海贫血(地贫)患儿体内铁代谢和红细胞系造血状况。
He was also informed that, due to thalassemia gene deletion or mutation is caused by, but not its genetic transmission. 同时他还得知,地中海贫血由于是基因缺失或突变引起的,因此它遗传但不传染。
Prenatal Diagnosis of β-Thalassemia by PCR and Dot Blot 应用聚合酶链反应与斑点印迹杂交产前诊断β地中海贫血
Detection of β-thalassemia by Suspension Array Technology and Denaturing High-Performance Liquid Chromatography 应用悬浮点阵和变性高效液相色谱技术检测β地中海贫血基因的比较
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
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。
Objective To investigate the carrier rate of thalassemia gene in children with decreased mean corpuscular volume ( MCV). 目的了解平均红细胞体积(MCV)降低儿童的珠蛋白生成障碍贫血(地贫)基因携带率。
The Best Threshold Value of Hemoglobin A_2 for Diagnosis of β-Thalassemia Carriers by High Performance Liquid Chromatography 高效液相色谱法检测血红蛋白A2诊断β-地中海贫血携带者的最佳阈值
Raman Spectroscopy-Based Study of the Discrimination and Oxygen Carrying Capacity of Thalassemia Erythrocytes 基于拉曼光谱的地中海贫血红细胞判别和携氧功能研究
Investigation of the Incidence of Thalassemia in the East of Shenzhen City 深圳东部地区地中海贫血发病率的调查研究
Analysis of β-thalassemia Mutation in east area of Sichuan 四川东部地区β地中海贫血基因突变分析
Conclusions Both MCV and erythrocyte fragility can serve as markers for the diagnosis of neonatal thalassemia, and MCV appears to be a better one. 结论MCV和红细胞脆性均可作为新生儿地贫诊断的有效指标,且MCV的诊断价值优于红细胞脆性。
Study of the Parathyroid Gland Function in Thalassemia Children 地中海贫血儿童甲状旁腺功能的研究
DNA methylation in β-thalassemia by oligonucleotide microarray 基于寡核苷酸芯片的β-地中海贫血DNA甲基化的研究
Aanalysis and clinical significance of serum lactate dehydrogenase activity in patients with Thalassemia 地中海贫血患儿血清乳酸脱氢酶活性分析及临床意义
Pedigree analysis of the double heterozygote of hemoglobin G disease combined with alpha thalassemia 2 血红蛋白G病复合α地中海贫血2的家系分析
The Impact of Splenectomy to Thalassemia Children's Humoral and Cell-mediated Immunity 脾切除术对地中海贫血儿童体液和细胞免疫功能的影响
Analysis on types of gene mutation in 184 patients with β-thalassemia in Baise 百色地区184例β-地中海贫血患儿基因突变类型分析
Objective To explore the value of red blood cell parameters ( MCV/ RDW) and red blood cell morphology combined detection in thalassemia diagnosis. 目的探讨红细胞参数(MCV/RDW)和红细胞形态学联合检测在地中海贫血诊断中的应用价值。
Meta-analysis of the efficacy and safety of combined therapy with deferiprone and deferoxamine in thalassemia major patients 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
Investigation the carrier rate and fetal diagnosis of thalassemia in zhanjiang city 湛江地区地中海贫血基因携带率及产前基因诊断的研究
Beta thalassemia on children: the molecular basis and treatment 儿童β地中海贫血的分子基础和治疗
Study of prenatal diagnosis in α-thalassemia by non-invasive method based on oligonucleotide microarray 利用寡核苷酸芯片诊断α-地中海贫血无创方法的探讨
Objective To detect the type of gene mutation of thalassemia in Kunming city. 目的探讨昆明市珠蛋白生成障碍贫血(地贫)的基因突变类型。
Lead Exposure from Transfusion Therapy in Children with Thalassemia in Industrial City 工业城市地中海贫血患儿输血治疗的血源性铅暴露
Objective: To study the rate of the combined tests of thalassemia and G6PD deficiency in detection of before marriage, to direct aristogenesis and good brood. 目的探讨地中海贫血和G6PD缺乏联合检测在婚前检查中的发病率,并指导优生优育。
Single-Cell Raman Spectral Analysis of Oxygenated and Deoxygenated Thalassemia Erythrocytes 单细胞拉曼光谱分析地中海贫血红细胞的氧合态和去氧态
Diagnosis of β-thalassemia by single cell nested polymerase chain reaction 单细胞巢式聚合酶链反应诊断β地中海贫血