hemolytic anemia的例句大全

relationship between genetic mutations of glucose-6-phosphate dehydrogenase deficiency and infantile acute hemolytic anemia in changsha city

长沙地区婴幼儿G6PD基因突变与急性溶血性贫血关系的研究

minerals are important for normal hematopoiesis and may play a role in acute hemolytic anemia induced by g6pd deficiency.

矿物质对正常血作用而言是重要的，而且其在G6PD缺乏造成之急性溶血性贫血可能扮演某些角色。

all these cases had acute hemolytic anemia, jaundice, hemoglobinuria and reduced g6pd activity to different extents.

所有患者都具有急性溶血性贫血，黄疸等临床表现及不同程度的血红蛋白尿、G6PD酶活性降低。

objective to understand gene mutant types of glucose 6 phosphate dehydrogenase ( g 6 pd) deficiency among local guangdong children and to evaluate the method using dried blood spots on filter paper in examination of patients suffered from acute hemolytic anemia caused by g 6 pd deficiency.

目的了解广东人葡萄糖6磷酸脱氢酶（G6PD）缺陷的基因突变型。

the application of microcolumn coomb's test in the diagnosis of autoimmune hemolytic anemia

凝胶直接抗球蛋白试验在自身免疫性溶血性贫血实验诊断中的应用

Occasionally, it may be seen with hemolytic anemia, porphyria cutanea tarda, excessive oral iron ingestion, or chronic alcoholism.

偶尔，可以看到有溶血性贫血、迟发性皮肤卟啉、铁摄取过量口服或慢性酒精中毒。

In recent 10 years, pulse_dose methylprednisolone combined with anticoagulation therapied and early preventive dialysis were discovered to be the measures conductive to put the microangiopathic hemolytic anemia ( MAHA) under control and improve the renal function.

近10年采用甲基泼尼松龙冲击配合抗凝疗法及早期实施预防性透析治疗对控制微血管性溶血性贫血和改善肾功能有效。

Postpartum hemolytic uremic syndrome is a complication that present with microangiopathic hemolytic anemia, thrombocytopenia, and acute kidney failure after delivery.

产后溶血性尿毒症综合征是指产后以急性微血管病性溶血性贫血、血小板减少及急性肾衰竭三大特征为主的综合征。

Objective Hemolytic uremic syndrome ( HUS) is characterized by the triad of thrombocytopenia, microangiopathic hemolytic anemia and acute renal failure.

目的溶血尿毒综合征（Hemolytic uremic syndrome，HUS）是一种以溶血性贫血、血小板减少和肾功能衰竭三联征为主要临床特点的疾病。

Objective To study the significance of the micro blood sample for surface antibody of red blood cells ( RBC) in the diagnosis of childhood autoimmune hemolytic anemia ( AIHA).

目的采用微量血检测自身免疫性溶血性贫血（AIHA）患儿的红细胞表面抗体，对其方法学与诊断学进行探讨。

Objective: To investigate the incidence and profile of adverse drug reactions ( ADRs) of puerarin injection, and explore the mechanism of Hemolytic Anemia ( HA) ADR due to puerarin.

目的：研究葛根素注射剂（GGS）引起的药物不良反应（ADR）发生率、ADR类型，探索GGS引起的溶血性贫血（hemolytic anemia，HA）的发生机制。

Objective The study was conducted to evaluate the diagnostic value of the mean corpuscular hemoglobin concentration ( MCHC) in hemolytic anemia ( HA).

目的观察平均红细胞血红蛋白浓度（MCHC）检测对溶血性贫血（HA）的诊断价值。

Hereditary non-spherocytic hemolytic anemia and clinic ( 4 cases reported)

遗传性非球形细胞溶血性贫血与临床研究（附4例报告）

Detection and Discuss of Neonatal Hemolytic Anemia Caused by Maternal-Fetal ABO Incompatibility

母婴ABO血型不配合引起的新生儿溶血病检测与讨论

in intravascular hemolytic anemia, more rbc are destroyed in the circulation (hemoglobinemia) than can be bound to haptoglobin.

当发生血管内溶血性贫血，更多红细胞在血液循环（血红蛋白血症）被破坏以至于超出肝球蛋白质的结合能力。

erythrocyte metabolism and antioxidant status of patients with wilson disease with hemolytic anemia

Wilson病合并溶血性贫血患者的红细胞代谢及抗氧化物水平

an analysis of relapse and risk factors of autoimmune hemolytic anemia and evans syndrome

自身免疫性溶血性贫血和Evans综合征复发及其相关因素分析

influences of reinforcing kidney drugs on dna and rna of immaturity red blood cells in bone marrow of mice with hemolytic anemia

补肾生血中药对溶血性贫血小鼠骨髓幼稚红细胞DNA和RNA影响

objective to evaluate the clinical implications of igg subclass in autoimmune hemolytic anemia ( aiha).

目的研究温抗体型自身免疫性溶血性贫血IgG亚型及其临床意义。

identification of abo and rh blood group in patients with autoimmune hemolytic anemia

自身免疫溶血性贫血患者ABO及Rh血型鉴定