thalassemia
英式音标：[θælə\'si:mɪə] 美式音标：[θælə\'simɪr]
thalassemia基本解释 n. 地中海贫血；库利氏贫血 thalassemia的意思释义 n.珠蛋白生成障碍性贫
thalassemia怎么读
英式音标：[θælə\'si:mɪə]
美式音标：[θælə\'simɪr]
thalassemia基本解释
n. 地中海贫血；库利氏贫血
thalassemia的意思释义
n.
珠蛋白生成障碍性贫血；
英英释义
thalassemia[ ,θælə\'si:miə ]n.an inherited form of anemia caused by faulty synthesis of hemoglobin
同义词：thalassaemiaMediterranean anemiaMediterranean anaemia
thalassemia用法及例句
双语例句
用作名词(n.)
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。
Recently, the team reported the first case of successful non-myeloablative matched unrelated stem cell transplantation in a thalassemia major patient.
较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。
例句参考
Role of γG XmnI polymorphism in thalassemia intermedia patientsBone Marrow Transplantation in Patients with Thalassemia
Survival in medically treated patients with homozygous beta-thalassemia.
Survival and complications in patients with thalassemia major treated with transfusion and deferoxamine
Related umbilical cord blood transplantation in patients with thalassemia and sickle cell disease
Cardiac T2* Magnetic Resonance for Prediction of Cardiac Complications in Thalassemia Major
HbVar: A relational database of human hemoglobin variants and thalassemia mutations at the globin gene server
Long-term safety and effectiveness of iron-chelation therapy with deferiprone for thalassemia major.
Randomized controlled trial of deferiprone or deferoxamine in beta-thalassemia major patients with asymptomatic myocardial siderosis
Mutations in a putative global transcriptional regulator cause X-linked mental retardation with alpha-thalassemia (ATR-X syndrome).
thalassemia词源
thalassemia (n.)
from thalasso- \"sea\" + haima \"blood\" (see -emia).
thalassemia相关例句
1. Other anemias. There are several other, rarer forms of anemia, such as thalassemia and anemias caused by defective hemoglobin.
其它类型比如地中海贫血、血红蛋白病等相对较为罕见的类型。
2. Diseases such as sickle cell anemia and beta thalassemia result from abnormal red blood cells and can be treated with bone-marrow transplants.
诸如因为先天性恶性红细胞而导致的贫血都可以通过骨髓移植解决。
3. The medicines now under threat are for childcare, in the maternity departments, and for conditions such as cancer, epilepsy, haemophilia and thalassemia.
现在供应颇为紧张的是产科的儿童保育用药及癌症、癫痫、血友病、地中海贫血病用药。
5. 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。
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6. 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。
7. 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。
8. Thalassemia is considered a kind of heritable hemolytic disease with high heterology.
地中海贫血是一组高度异质性的遗传性溶血性疾病。
9. Objective:To study the relationship between mean corpuscular volume(MCV), mean corpuscular hemoglobin(MCH) of umbilical blood and thalassemia.
目的：探讨新生儿脐血红细胞平均体积（MCV）和红细胞平均血红蛋白（MCH）与地中海贫血的关系。
10. Objective To investigate the incidence and types of genic mutations for thalassemia in Shenzhen area and perform the prenatal diagnosis in high risk fetus.
目的调查深圳市孕妇地中海贫血发病率、基因突变类型，对高风险胎儿进行产前诊断。
11. Conclusion The simple and quick blood test, in particular, MCV, RDW of iron deficiency anemia and thalassemia clinical identification, have some diagnostic value, should be applied.
结论简便、快捷的血常规检测，尤其MCV，RDW对缺铁性贫血和地中海贫血的临床鉴别，有一定诊断价值，值得应用。
12. Methods A retrospective analysis, statistical analysis of 80 patients with iron deficiency anemia, 30 patients with thalassemia patients and 100 healthy blood test medical staff changes.
方法采用回顾性分析的方法，统计分析了80例缺铁性贫血患者，30例地中海贫血患者及100例健康体检人员的血常规检查的变化情况。
13. Probably because it is itself so my lip thalassemia have been a bit like a darker color red purple side first meeting so often they say are you okay?
可能因为是本身有地中海贫血所以我的唇色一直都偏深颜色有点像偏紫的红所以第一次见面常被人家说你还好吧？
16. Methods: Using mon-vessel screen method of thalassemia and relative value of G6PD detect thalassemia and G6PD deficiency for man and woman of detection of before marriage in 4268 duplet.
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。
17. Objective To investigate the clinical significance of automated reticulocyte multiple parameters analysis in thalassemia patients.
目的：探讨网织红细胞参数在地中海贫血检测的临床意义。
18. Objective: To using umbilical blood detect the thalassemia to neonate.
目的应用脐血对新生儿进行地中海贫血的筛查。
19. Objective To investigate the effects and side reaction of hydroxyurea on HbE/β-thalassemia patients, then explore the correlated factors between hydroxyurea with fetal hemoglobin and total hemoglobin.
目的：观察羟基脲对血红蛋白E/β-地中海贫血患者的疗效及毒副作用，寻找羟基脲提高胎儿血红蛋白与总的血红蛋白的相关因素。
20. ObjectiveTo explore the changes of reticulocyte multiple parameters and their clinical significance in patients with thalassemia minor.
目的探讨轻型地中海贫血患者网织红细胞参数的变化及临床意义。
21. Objective:To approach the value and applicability of the activity of Glucose-6-phosphate dehydrogenase (G6PD) for the auxiliary diagnosis of thalassemia.
目的：探讨葡萄糖六磷酸脱氢酶（G6PD）活性对地中海贫血（地贫）的辅助诊断价值及其适用范围。
22. Objective:To evaluate the application of multiple polymerase chain reaction(multiple PCR)and PCR/reverse dot blot(RDB)in gene diagnosis of thalassemia.
目的：探讨多重PCR和PCR/反向点杂交（RDB）在珠蛋白生成障碍性贫血基因诊断中的应用。
23. 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。
24. 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。
25. Objective To investigate the feasibility of bone marrow hematopoietic stem cell transplantation in treating β-thalassemia major.
目的探讨骨髓移植治疗重型地中海贫血的可行性。
26. A usually fatal form of thalassemia in which normal hemoglobin is absent, characterized by severe anemia, enlargement of the heart, liver, and spleen, and skeletal deformation.
库利氏贫血病：一种通常能致命的地中海贫血病，患者无正常的镰刀细胞血红素，症状为严重贫血，心脏、肺及脾变大并且骨骼变形。
28. Objective To explore the value and applicability of the activity of glucose-6 phosphate dehydrogenase(G-6PD) for the auxiliary diagnosis of thalassemia.
目的探讨葡萄糖-6磷酸脱氢酶（G-6PD）活性对珠蛋白生成障碍性贫血（地贫）的辅助诊断价值及其适用范围。
29. Objectives To evaluate the early diagnosis way of thalassemia major.
评价重型地中海贫血（地贫）的早期诊断方法。
30. Human umbilical cord blood (UCB) has plenty of hematopoietic stem cells (HSCs) and can be used in the cure of leukaemia, malignancy and thalassemia major.
脐血中含有丰富的造血干细胞，可以治疗白血病、恶性肿瘤、重型地中海贫血等多种疾病。
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31.thalassemia anemia
库利氏贫血
32.a fatal form of thalassemia in which there is no hemoglobin; skeletal deformations; heart and spleen and liver enlarged.
没有血色素的一种贫血症。
34.minor thalassemia
轻地中海型贫血
35.major thalassemia
重地中海型贫血
36.To study the types and frequency of gene mutations ofβ- thalassemia in Jiangxi area.
目的探讨江西地区β中海贫血基因突变类型及其频率。
-- 来源 -- dict.cnki.net
