thalassemia是什么意思   thalassemia怎么读

英式:[θælə'si:mɪə]    美式:[θælə'si:mɪə]

thalassemia单词基本解析:

n.珠蛋白生成障碍性贫血
n. 地中海贫血
n.珠蛋白生成障碍性贫血;

thalassemia变化用词:


形容词: thalassemic |

thalassemia英英释义:

Noun

1. an inherited form of anemia caused by faulty synthesis of hemoglobin

名词 thalassemia:

an inherited form of anemia caused by faulty synthesis of hemoglobin

同义词:thalassaemia, Mediterranean anemia, Mediterranean anaemia



thalassemia[ ,θælə'si:miə ]n.an inherited form of anemia caused by faulty synthesis of hemoglobin

同义词:thalassaemiaMediterranean anemiaMediterranean anaemia

thalassemia中文词源:

thalassemia用法和例句:

We found 10 types of rnutation and 28 com - pound genotypes of � � - thalassemia.

结果表明,有10种β地中海贫血珠蛋白基因突变类型和28种β珠蛋白突变基因的组合形式.

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To study the types and frequency of gene mutations of � � - 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.

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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.

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thalassemia


A/gamma/ delta beta0 Thalassemia

A/γ/δβ0地中海贫血


F thalassemia

F-地中海贫血


Keywords G6PD activity;Auxiliary diagnosis;Thalassemia;

G6PD活性;辅助诊断;地中海贫血;


Hb Lepore thalassemia

Hb Lepore地中海贫血


HPFH A gamma beta+ thalassemia

HPFH A γβ+地中海贫血


HPFH G gamma beta+ thalassemia

HPFH Gγβ+ 地中海贫血


HPFH delta beta0 thalassemia

HPFH δβ0地中海贫血


thalassemia minima

[医] 极轻型地中海贫血


thalassemia minor

[医] 轻型地中海贫血


alpha+ Thalassemia

α+地中海贫血


α - thalassemia

α-地中海贫血


alpha0 Thalassemia

α0地中海贫血


alpha Thalassemia

α地中海贫血


alpha Thalassemia 1

α地中海贫血 1


alpha Thalassemia 2

α地中海贫血 2


beta+ Thalassemia

β+地中海贫血


beta- thalassemia

β-地中海贫血


beta0 Thalassemia

β0地中海贫血


beta Thalassemia

β地中海贫血


delta0 Thalassemia

δ0地中海贫血


delta beta0 Thalassemia

δβ0地中海贫血


delta beta Thalassemia

δβ地中海贫血


delta Thalassemia

δ地中海贫血


epsilon gamma delta beta Thalassemia

εγδβ地中海贫血


thalassemia intermedia

中间型地中海贫血


Keywords thalassemia intermedia;polymerase chain reaction;reverse dot blot hybridization;prenatal diagnosis;

中间型地中海贫血;聚合酶链反应;反向斑点杂交;产前诊断;


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;


human thalassemia

人地中海贫血


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'?


they are suffering from thalassemia, such as hemophilia or blood disease;

他们因为患血友病或地中海贫血等血液病;


Keywords Thalassemia;Hemoglobin electrophoresis;MCV;RDW;

关键词地中海贫血;血红蛋白电泳;MCV;RDW;


simple thalassemia

单纯型β地中海贫血


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。


Keywords deferiprone;deferoxamine;thalassemia;ferritin;iron;

去铁酮;去铁胺;地中海贫血;铁蛋白;铁;


The assessment of Effectiveness and Safety of Combined Therapy with Deferiprone and Deferrioxamine in Patients with Thalassemia Major

去铁酮和去铁胺联合治疗重症地中海贫血的安全性和有效性评估


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。


Beta - thalassemia

地中海贫血


Keywords Thalassemia;G6PD deficiency;Aristogenesis and good brood;

地中海贫血;G6PD缺乏;优生优育;


Keywords Thalassemia;Antenatal examination;Meam corpuscular volume;Red cell osmotic fragility;Hemoglobin electrophoresis;

地中海贫血;产前筛查;红细胞平均体积;红细胞脆性试验;血红蛋白电泳;


Keywords Thalassemia;Gene;Heterozygote;Polymerase chain reaction;Reverse dot blot;

地中海贫血;基因;杂合子;聚合酶链反应;反向点杂交;


Keywords Thalassemia;DNA microarray;Gene diagnosis;

地中海贫血;基因芯片;基因诊断;


Keywords thalassemia;gene diagnosis;clinical manifestation;

地中海贫血;基因诊断;临床分析;


Keywords beta Thalassemia;Globins;Gene expression;Indoles;

地中海贫血;珠蛋白类;基因表达;吲哚类;


Keywords Thalassemia;screening;MCV;Cutoff value;

地中海贫血;筛查;MCV;截断值;


Keywords beta Thalassemia;Polymerasa chain reaction;Parents Genes;mutation;

地中海贫血;聚合酶链反应;双亲;基因;突变;


Keywords Thalassemia;Polymerase chain reaction;Oligomuleotide array seguence analysis;

地中海贫血;聚合酶链反应;寡核苷酸;序列分析;


Keywords Alpha thalassemia;Polymerase chain reaction;Genetic screening;Prenatal diagnosin;

地中海贫血;聚合酶链式反应;遗传筛查;产前诊断;


Keywords Thalassemia;Serum iron;Mean corpuscular volume;

地中海贫血;血清铁;红细胞平均体积;


Study of prenatal screening and gene diagnosis of thalassemia

地中海贫血产前筛查及基因诊断研究


Gene Diagnosis, Carrier Detecting and Prenatal Diagnosis for Thalassemia

地中海贫血基因诊断、携带者检查、产前诊断


Thalassemia family marriage and birth defect intervene

地中海贫血家系婚配与出生缺陷干预


ulcer of the leg in thalassemia

地中海贫血性小腿溃疡


Observations on erythrocyte parameters and histograms from patients with thalassemia

地中海贫血患者红细胞参数及直方图观察


The significance of automated reticulocyte multiple parameters analysis in patients with thalassemia

地中海贫血患者网织红细胞多参数分析的意义


An Analysis of Blood-lipid and Apolipoprotein in? Thalassemia Patients

地中海贫血患者血脂及载脂蛋白分析


Thalassemia trait

地中海贫血特征


Thalassemia genotyping and comparison of two diagnostic reagent

地中海贫血的基因诊断及两种试剂比较


thalassemia syndrome

地中海贫血综合征, 库利(氏)贫血, 遗传性薄红细胞增多


Relationship between the genotype and hematologic characteristics in the fetuses with thalassemia

地中海贫血胎儿产前基因型诊断结果与血象特点的分析


Ascertaining and Application of Cutoff Values of Mean Corpuscular Volume and Mean Hemoglobin Concentration in Positive Thalassemia Phenotype People

地中海贫血表型阳性平均红细胞体积和平均血红蛋白浓度截断值及应用


Abnormalities of the erythrocyte membrane ultrastructure and the membrane proteins in a patient with HEMPAS, alpha thalassemia and complicated diabetes

型先天性红细胞生成异常性贫血患者红细胞膜超微结构和膜蛋白变化


complex thalassemia

复合型地中海贫血


Screeing and diagnostic of childbirth front for thalassemia in the crowd of wed front check

婚检人群地中海贫血筛查与产前诊断


Keywords Microcytosis;Thalassemia;Iron-deficiency anemia;Red cell osmotic fragility tests;Molecular diagnosis;

小红细胞症;地中海贫血;缺铁性贫血;红细胞渗透脆性试验;分子诊断;


Comparison between mean corpuscular volume stereometry and simple tube red cell osmotic fragility quantitative test in antepartum detection of Thalassemia

平均红细胞体积测定法与红细胞脆性一管定量法用于地中海贫血产前筛查的比较


Study on the screening program of thalassemia and the genotype and hematologic parameter among people of productive age in a village, Nanning Guangxi

广西南宁市农村育龄人群地中海贫血筛查及基因型和血液学参数分析


thalassemia anemia

库利氏贫血


Cooley anemia, thalassemia

库利贫血, 地中海贫血, 珠蛋白生成障碍性贫血


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。


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。


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。


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。


Heterozygous thalassemia

杂合子性地中海贫血


Keywords preimplantation genetic diagnosis;nested-polym erase chain reaction;whole genome amplification;primer extension preamplific ation;embryo biopsy;thalassemia;

植入前遗传学诊断;巢式-聚合酶链反应;全基因组扩增;扩增前引物延伸法;胚胎活检;地中海贫血;


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。


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.中国优生与遗传杂志,2003,11(1):107.


a fatal form of thalassemia in which there is no hemoglobin

没有血色素的一种贫血症


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。


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。


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

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.
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。