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- In fact, couples are able thalassemia gene carriers. 原来，余力夫妇都是地中海贫血基因的携带者。
- METHODS Using the auantitative method to detect the riemolysts rate of thalassemia. 方法用地中海贫血一管定量法,查出地中海贫血溶血率。
- Hajjar FM,Pearson HA.Pharmacologic treatment of of thalassemia intermedia with hydroxyurea. 程少杰;朱为国;钱新华.;脾栓塞治疗地中海贫血的并发症
- 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。
- The Hematology Lab is responsible for blood and bone marrow cytology tests, Diabetes and Thalassemia tests. 临床血液室负责血细胞、骨髓细胞学检查及糖尿病和地贫项目的检验；
- Free erythrocyte Protoporphyrin(FEP)were determined in 116 thalassemia patients,37 iron deficiency anemia patients and 45 normal subjects. 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。
- Recently, the team reported the first case of successful non-myeloablative matched unrelated stem cell transplantation in a thalassemia major patient. 最近成功完成了国际首例非清髓，非血缘供者造血干细胞移植治疗重型地中海贫血。
- Thalassemia (American English) or thalassaemia (British English) is a dominant trait inherited disease of the red blood cells. 什么是'地中海贫血中间-遗传性疾病导致贫血'?
- Following the development of molecular biology in thalassemia,the state in gene defect of thalassemia in china becomes more and more clear. 随着地中海贫血(地贫)分子生物学的研究进展,地贫基因缺陷状况也愈来愈清晰地显露出来。
- Rogers M,Phelan L,Bain B.Screening criteria fOr beta thalassemia trait in pregnant women.J Clin Pathol,1995,48(11):1054. 江肖兴;麦霭君.;平均红细胞体积筛查妊娠合并地中海贫血的价值
- In addition, serious impact on family health and stability of many genetic diseases, such as hemophilia, thalassemia, Down's syndrome, and so on. 此外，严重影响家庭健康和稳定的遗传性疾病也很多，如血友病、地中海贫血、唐氏综合症等等。
- 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。
- The hemoglobin disorders of thalassemia is the most prevalent group of human monogenic diseases,which results from globin protein chain peptide synthesis imbalance. 地中海贫血是最常见的单基因遗传病,它是由于珠蛋白肽链合成量之间不平衡导致,所以纠正珠蛋白肽链失衡成为地中海贫血治疗研究的关键。
- Mediterranean anemia(thalassemia),occurring relatively often in southern China,is a genetic and hemolytic disease induced by disfunction of globin synthesis. 地中海贫血是我国南方常见的因珠蛋白合成障碍所致的遗传性溶血性疾病。
- Clinic Test Observation of New Types of Thalassemia Hemoglobinopathy Syndrom. It won the 2nd prize of "Guangxi scientific and technological progress" in 1994,Experment in Process. 抗人甲胎蛋白单克隆抗体的研制和应用研究1997年获广西科技进步二等奖。图为研究人员进行检测。
- Objective: To evaluate the safety and efficacy of combining deferiprone(DFP)and deferoxamine(DFO)in iron chelation therapy in patients with thalassemia. 目的:探讨去铁酮(DFP)和去铁胺(DFO)联合用药对重症地中海贫血螯合治疗的安全性和有效性。
- Many genetic diseases that can be used PGD to prevent the generations to come, such as hemophilia, color blindness, thalassemia, Down's syndrome and so on. 很多遗传性疾病都可以使用这种PGD方法避免遗传给后代，譬如血友病、色盲、地中海贫血、先天愚型等等。
- 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。方法应用地中海贫血一管筛查法和G6PD比值法检测4268对婚前男女的地中海贫血和G6PD缺乏。
- Leukemia, cancer, aplastic anemia, thalassemia, muscular dystrophy, there are other diseases such as glaucoma patients, can also be used over the same treatment modalities. 白血病、癌症、再生障碍性贫血、地中海贫血、进行性肌营养不良，还有青光眼等其他病症的患者，同样也可以采用以上救治方式。
- Our study demonstrated that the implementation of national health insurance program may play an important role in the decrease of both prevalence and incidence rates of thalassemia major in Taiwan. 本研究显示台湾罹患重型乙型海洋性贫血病患于全民健保实施后明显减少，而对于重型乙型海洋性贫血病患的照顾虽有进步，但仍有努力的空间。
