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In sickle-cell disease, the haemoglobin is abnormal and this causes a change in the shape of the red blood cells.

在镰状细胞病,血红蛋白是不正常的,这造成的改变形状的红血细胞。

Not as much analysis has been completed on the children's cases, but health officials noted that 6 per cent were kids with sickle-cell disease or another condition from the same family of blood diseases.

没有那么多的分析已经完成了对儿童的个案,但卫生官员指出,百分之6例镰状细胞病或另一血液疾病的同一家庭状况的孩子。

OBJECTIVE: To alert the medical community about this unusual association of infectious diseases in a healthy patient without sickling or immunosuppression.

目的:警告医学界在没有镰状红细胞改变或免疫抑制的健康病人,这种罕见的感染性疾病的联合。

SUMMARY OF BACKGROUND DATA: Human leptospirosis has been intensively studied, and there are several reports of salmonella vertebral osteomyelitis in patients without sickling.

背景数据信息概要:人类钩端螺旋体病的研究很多,也有一些无镰状红细胞改变的病人发生沙门氏菌性脊椎骨髓炎的报道。

Those include the most prevalent types of leukemia, metabolic disorders like Tay-Sachs disease, blood-related conditions such as sickle cell anemia and severe anemia problems.

这些措施包括最普遍的类型的白血病,代谢性疾病一样,泰-萨克斯疾病,血液相关的条件,如镰状细胞性贫血和严重贫的问题。

Heterozygote screening : Screening a susceptible population (eg, Tay-Sachs disease in Ashkenazic Jews, sickle cell anemia in blacks, thalassemia in various ethnic groups) may be appropriate because of the high frequency of heterozygotes.

杂合子筛查由于某些易患人群中有较高的杂合子发生率,在他们中筛查某些疾病是合适的(如在以色列的阿斯克那士犹太人中查Tay-Sachs病,黑人中查镰状细胞贫血,少数民族中查地中海贫血)。

Heterozygote screening : Screening a susceptible population (eg, Tay-Sachs disease in Ashkenazic Jews, sickle cell anemia in blacks, thala emia in various ethnic grou ) may be a ropriate because of the high frequency of heterozygotes.

杂合子筛查由于某些易患人群中有较高的杂合子发生率,在他们中筛查某些疾病是合适的(如在以色列的阿斯克那士犹太人中查Tay-Sachs病,黑人中查镰状细胞贫血,少数民族中查地中海贫血)。

While symptoms may seem to improve almost immediately after surgery, it takes approximately 6-12 months before new vessels develop sufficiently. Diseases associated with moyamoya include sickle cell anemia, atherosclerosis, prior radiation therapy to the skull base in children, and less commonly neurofibromatosis, tuberous sclerosis, meningitis, retinitis pigmentosa, fibromuscular dysplasia, Down's syndrome and Fanconi's anemia.

手术之后几乎立即可以看到症状的好转,新的血供充分发展起来大概要花6-12月时间。moyamoya相关的疾病包括镰状细胞性贫血、动脉粥样硬化、颅底部放疗,不太常见的有神经纤维瘤病,结节性硬化、脑膜炎、色素性视网膜炎、纤维性肌发育不良、Down氏综合症和Fanconi's 贫血症

Methods:All cases of nasal alar defect that were repaired by auricular composite graft.temporal L shape shin flap、tubed shin flap、z-plasty by residual nasal ala.expanded forehead flap and full-thickness skin graft,were reviewed and analyzed.

对既往采用的耳廓复合组织瓣、颞部镰状皮瓣、残存鼻翼的局部皮瓣、上臂内侧皮管、额部扩张皮瓣及全厚皮片所修复的鼻翼缺损共48个病例进行回顾性分析。

A protocol for nonmyeloablative allogeneic hematopoietic stem-cell transplantation that includes total-body irradiation and treatment with alemtuzumab and sirolimus can achieve stable, mixed donor-recipient chimerism and reverse the sickle cell phenotype.

包括全身照射以及阿仑单抗和西罗莫司治疗在内的非清髓性异基因造血干细胞移植方案,可取得稳定的混合供者—受者嵌合性,并且可逆转镰状细胞表型。

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