贫血

Infants aged 3 months tol year were the high-risk population of iron deficiency anemia.

3月龄～1岁的婴幼儿是缺铁性贫血的高发人群。

The ability of bacteria to be genetically transformable.

由于血色素合成有误引起的遗传性贫血症。

Methods The present study included twelve undialyzed ESRD patients with anemia.The sera from the uremic patients were added to CFU-E and BFU-E culture in the concentrations ranging from 1.25% to 5%.In vitro CFU-E and BFU-E growth in the presence of sera from ESRD patients was compared with in the presence normal human subjects with the use of normal mice bone marrows.

选择12例尿毒症肾性贫血未透析患者为试验组，另选正常健康体检者12例为正常对照组，将实验组、正常对照组血清分别稀释成不同终浓度，采用甲基纤维素细胞培养的方法对小鼠骨髓细胞进行培养，对比不同浓度血清组红系集落形成单位、红系爆式形成单位的集落数。

objective to investigate the existence of the erythropoiesis inhibitors.methods the present study included twelve undialyzed esrd patients with anemia.the sera from the uremic patients were added to cfu-e and bfu-e culture in the concentrations ranging from 1.25% to 5%.in vitro cfu-e and bfu-e growth in the presence of sera from esrd patients was compared with in the presence normal human subjects with the use of normal mice bone marrows.results the effects of the sera from uremic patients on cfu-e and bfu-e colony growth in concentrations ranging from 1.25% to 5% were investigated to be dose-dependent.the effect increased with the concentrations increasing of the sera（p＜0.05）.there were not significant inhibitory effect on the cfu-e and bfu-e growth of mice bone marrow in vitro from sera of the normal subjects.conclusion the erythropoiesis inhibitors exist in uremic sera which has a dose-dependent inhibitive effects on the growth cfu-e and bfu-e of normal mice bone marrow cells.

选择12例尿毒症肾性贫血未透析患者为试验组，另选正常健康体检者12例为正常对照组，将实验组、正常对照组血清分别稀释成不同终浓度，采用甲基纤维素细胞培养的方法对小鼠骨髓细胞进行培养，对比不同浓度血清组红系集落形成单位、红系爆式形成单位的集落数。结果在实验组中，与血清浓度为0的浓度组相比，与各浓度组血清共同培养的小鼠骨髓cfu-e和bfu-e的集落数均明显减少，且随血清浓度的增加，小鼠骨髓cfu-e和bfu-e的集落数逐渐减少，各浓度组间差异有显著性（p＜0.05）。结论尿毒症患者血清抑制小鼠骨髓红系祖细胞集落形成，随患者血清浓度的增加，抑制作用增强，具有剂量依赖性。

HbJ Tashikuergan was firstly reported in the world, and CD8and CDs8/9 were firstly discovered in China.Conclusion:The types and distribution of abnormal hemoglobin and thalassemia in Kashi district were? different from those in other areas of our country,and also unsimilar to our neighbour countries.

对喀什地区血红蛋白病的研究表明，异常血红蛋白和地中海贫血的类型特点既有别于我国其它地区，又与邻近的中亚等国不完全相同，形成了该地区独有的遗传特征。

Gastrointestinal parasitism is characterized gastroenteritis, unthriftiness and anemia.

胃肠道寄生虫病的特征是：胃肠炎，瘦弱和贫血。

Haemolytic uraemic syndrome is characterized by the triad of microangiopathic haemolytic anaemia, thrombocytopenia and acute renal failure.

溶血尿毒综合徵以微血管病性溶血性贫血，血小板减少症及急性肾功能衰竭三联症为特点。

Abstract］ Objective To compare with curative effect and adverse reaction on renal anemia of hemodialyses patients with Fe3dextran venously and ferromyn orally.

摘要］ 目的比较静脉注射右旋糖酐氢氧化铁和口服琥珀酸亚铁治疗血液透析患者肾性贫血的疗效和不良反应。

Abstract］ objective to compare with curative effect and adverse reaction on renal anemia of hemodialyses patients with fe3 dextran venously and ferromyn orally.methods 60 hd patients were divided into venous group and oral group randomly and there were 30 patients in each group,100 mg cosmofer were used one hour by vein point of dialyser before hd was completed in hemodialyses patients in venous group 200 mg amber acid subiron was taken by the patients in oral group three times a day and two months in total.recombinant human erythropoietine was used at a dose of 100～150 u/kg?

摘要］ 目的比较静脉注射右旋糖酐氢氧化铁和口服琥珀酸亚铁治疗血液透析患者肾性贫血的疗效和不良反应。方法选择60例hd患者，分为静脉补铁组和口服补铁组，每组30例。静脉补铁组：每次透析结束前1 h注射100 mg右旋糖酐氢氧化铁，从透析器静脉端输入，时间维持1 h；口服补铁组：琥珀酸亚铁200 mg，每日3次，连续口服2个月。两组同时使用基因重组人红细胞生成素100~150 u/kg？

Abstract］ Objective To compare with curative effect and adverse reaction on renal anemia of hemodialyses patients with Fe3dextran venously and ferromyn orally.

作者：赵晋媛，袁利，徐贵华，陈永华，李雁，谢平右旋糖酐氢氧化铁；肾性贫血；血液透析

Do you know, i need you to come back

你知道吗，我需要你回来

Yang yinshu、Wang xiangsheng、Li decang,The first discovery of haemaphysalis conicinna.

1〕 杨银书，王祥生，李德昌。安徽省首次发现嗜群血蜱。