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thalassanemia怎么读
thalassanemia的读音:[ˌθæləseiˈni:miə]
thalassanemia的意思
1、n.地中海贫血,库利氏贫血
thalassanemia的双语例句
1、Objective To evaluate the long term efficacy of partial splenic embolization ( PSE) for thalassanemia major.
目的评价部分性脾栓塞（Partial Splenic Embolization，PSE）治疗地中海贫血的长期疗效。
2、Gene Types in 252 Children Carried β-Thalassanemia
β地中海贫血患儿252例基因缺陷类型分析
3、Study of immune function in children with thalassanemia major after partial splenic embolization
部分性脾栓塞术对地中海贫血患儿免疫功能的影响
4、Long term efficacy of partial splenic embolization for thalassanemia major
部分性脾栓塞术治疗地中海贫血的长期疗效观察
5、Objective: To discuss the intervention of thalassanemia in Baise city.
目的：初步探讨广西省百色市地中海贫血干预模式。
6、The Value of Erythrocytic Parameters on Screening Thalassanemia in Prenatal Diagnosis
红细胞参数筛查地中海贫血在产前检查中的应用价值
7、Conclusions PSE is helpful for improving immunologic function of children with thalassanemia major.
结论PSE术有助于改善地中海贫血患儿的免疫功能。
8、Conclusion The total of 11 types of gene mutation in β-thalassanemia carriers are multiple in Shenzhen area.
结论深圳地区β地中海贫血患儿珠蛋白基因缺陷类型共有11种，呈现多样性。
9、Exploration of Tumor-like Hyperplasia in Extramedullary Hematopoietic Tissue of β-Thalassanemia Patients
β地中海贫血伴髓外造血组织瘤样增生的探讨
10、Objective To evaluate the changes of immunologic function in children with thalassanemia major after partial splenic embolization ( PSE).
目的探讨部分性脾栓塞术（PSE）对地中海贫血患儿免疫功能的影响。
11、The total effective rate was 86 7%, in which α,β thalassanemia major were 100 0%, 81 8% respectively.
总有效率为867%，其中α、β型地中海贫血患者的有效率分别为1000%、818%。
12、Objective To analyze the genes type in offspring of β-thalassanemia carriers in Shenzhen, and to provide evidence for related research and treatment.
目的分析深圳地区β地中海贫血（简称地贫）患儿珠蛋白基因缺陷类型，为开展相关的研究与治疗提供依据。
13、Result: The results of MCV, MCH and RDW showed significantly different between the thalassanemia group and the control group ( P < 0.01).
结果：地中海贫血组MCV、MCH、RDW与对照组比较有显著性统计学意义（P
14、For 36 cases, incision healed primarily, however, 6 cases belonged to secondary healing which included one case of diabetes and thalassanemia seperately.
36例术后伤口I期愈合，骨外露软件组织缺损覆盖修复满意，6例II期愈合，其中糖尿病，地中海贫血各一例。
15、Methods β-thalassanemia carriers were screened by using routine examination and the red cell osmotic fragility analysis. Hb electrophoresis and reverse dot blot hybridization were used to diagnose and analyze gene types.
方法通过血液常规检查和红细胞渗透脆性分析筛查地贫患儿，用血红蛋白电泳和基因诊断明确诊断并分析基因型。
16、The percentage of ones who received prenatal diagnosis improve 37% after the thalassanemia intervention, and 1 case among every 2.7 cases receiving prenatal diagnosis was achieved because of the intervention. 4 babies with severe thalassanemia were avoided.
干预后促进的产前诊断比干预前提高了37%，每2.7例产前诊断就有1例是由于预措施促成，并避免了4例重型地贫儿的出生。
17、To investigate the morphological features of mediastinal extramedullary hematopoietic tissue in β-thalassanemia patients and its diagnosis, the morphological features of tumor-like hyperplastic in extramedullary hematopoietic tissue were analyzed by using fine needle aspiration cytological ( FNAC) biopsy and compared with bone marrow smear sample.
为了研究β地中海贫血伴髓外造血组织瘤样增生细胞形态特点其及诊断，对纵隔髓外造血组织瘤样增生用细针抽吸活组织行细胞学检测（FNAC），并与骨髓片进行比较分析。
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