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红细胞增多

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The appearance of increased poikilocytosis, anisocytosis, and RBC inclusions suggests that a spleen is not present.

异形红细胞增多、红细胞大小不等以及红细胞内容物的出现均提示脾已不存在。

This CBC demonstrates findings suggestive of spherocytosis, a condition in which the RBC's are small and round (rather than the normal biconcave appearance) with increased hemoglobin content.

全血细胞计数提示球形红细胞增多症,其红细胞小而圆(而不是正常的双面平凹外观),且血红蛋白含量增加。

These findings support the importance of HIF-2 alpha in human Epo regulation and warrant investigation of HIF2A in patients with unexplained erythrocytosis.

这个发现支持HIF-2 alpha在红细胞生成素调节的重要作用,为研究不明原因的红细胞增多症病人的HIF2A提出了新的途径。

Objective: As an important adaptation mechanism to hypoxia, erythrocytosis resulting from high altitude hypoxia maintains an adequate Oa delivery in blood.

目的:高原缺氧时红细胞增多,红细胞适度增多可以改善组织供氧,是缺氧习服-适应的重要机制之一。

Methods OSAHS patients with and without erythrocytosis were 1∶3 matched in age, sex, the apnea/ventilation index,weigh index and diagnostic time.

收集 1 995年 1月至 2 0 0 2年 1 2月门诊及住院的OSAHS患者的资料,红细胞增多症病例组与无红细胞增多症对照组按年龄、性别、体质指数及就诊时间行 1∶3匹配。

Paradoxically,despite iron deficiency,there was erythrocytosis (red cell count 5.96*10 12/L;NR 3.8-4.8*10 12/L)indicating loss of homoeostatic control of erythropoiesis.

矛盾的是,虽然有铁缺乏,但仍存在红细胞增多症(红细胞计数5.96*10 12/L;NR 3.8-4.8*10 12/L)提示丧失了红细胞生成稳态的控制。

NEW YORK Feb 01 - Researchers have identified a myeloproliferative syndrome, defined by mutations in the Janus kinase 2 gene, that includes patients with a current diagnosis of polycythemia vera or idiopathic erythrocytosis.

纽约 二月一日-研究者已经确认了一种由Janus激酶2基因变异引起的新型骨髓增生综合症,这一症状现在被诊断为真性红细胞增多症或自发性红细胞红细胞增多

Methods Analyzed the clinical observation and nursing from 2004 to 2008 116 examples of monge disease patients,introduced the clinical manifestation,the prevention and the remedial measure with emphasis,as well as psychology and treatment and so on nursing.

回顾性分析2004年至2008年我院116例高原性红细胞增多症患者患病期间的临床观察和护理,重点介绍高原性红细胞增多症的临床表现、预防和治疗措施,以及心理及治疗等的护理。

In contrast to the homozygous mutated colonies seen with V617F-positive polycythemia vera, the colonies with this disorder featured heterozygous mutations.

V617F阳性的真性红细胞增多症的红细胞群落多为突变,与此对应的是:这类病症的红细胞群落以杂合变异为主要特征

To study the microrheological characteristics of RBCs underabnormal physiological conditions in vivo,a model of anemia models of rabbit induced by phenylhydrazine injection was built.

在Brunara等人用苯肼使动物造成急性溶血性贫血的方法基础上,建立一种由急性溶血性贫血后,而诱发家兔幼红细胞增多的非正常生理状态的红细胞在体衰老模型,继而研究新生红细胞从产生到死亡过程,即衰老过程的流变学特性的变化规律。

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