在包头市约1，000名汉族中，发现一例快泳异常血红蛋白。
A fast-moving abnormal hemoglobin was discovered in about 1, 000 Han men (Chinese) at Paotow.
本文报告广西地区发现的一个壮族异常血红蛋白家系的研究结果。
This paper presents the results of a study of abnormal hemoglobin on a family of Chuang ancestry in Guangxi region.
本文叙述了改进的硅胶薄板指纹图谱法用于异常血红蛋白结构分析中的肽段分离工作。
A modification of the thin-layer fingerprint procedure for the structural analysis of abnormal hemoglobin in red cells is described.
结论G 6 PD溶血虽然是自限性的，但当合并地中海贫血时，往往加重病情，尤其是某些特殊类型的异常血红蛋白。
ConclusionG6PD hemolysis is a self-limited disease, but it can grew worse when it is complicated by thalassemias, especially with some special types of abnormal hemoglobin.
它可以比较容易地分开血红蛋白a和血红蛋白f、可将异常血红蛋白分成两大类，即酸性电泳阳性和酸性电泳阴性两类异常血红蛋白。
Abnormal hemoglobin may be divided into two classes by acid AGAR gel electrophoresis. some variants may be separated from HbA by this method and others could not be separated from HbA.
他的团队探讨骨髓增生异常综合征的患者血红蛋白合成异常的情况。
His team investigated the state of abnormal composition of hemoprotein in myelodysplastic syndrome.
结论糖化血红蛋白异常与足溃疡风险程度密切相关，是足溃疡风险程度的影响因素。
Conclusion the abnormal glycosylated hemoglobin was closely related to level of risk in foot ulcers. It was the impacted factors to level of risk.
目的：探讨血细胞膜表面糖基磷脂酰肌醇（GPI）锚蛋白分子表达异常在诊断阵发性睡眠性血红蛋白尿症（PNH）时的意义。
Objective:To detect the expression of glycosyl phosphatidyl inositol (GPI) anchored protein on the blood cell membrane and its implication in the diagnosis of paroxysmal nocturnal hemoglobinuria(PNH).
营养状况与血红蛋白及血清蛋白异常率呈正相关，中度营养不良重病人的白球比值倒置比例明显增高。
The nutritional status was well compared with the abnormal ratio of hemoglobin and serum protein, and A/G reverse was increased in some middle malnutrition patients.
糖化血红蛋白异常与足溃疡风险程度正相关。
The correlation between abnormal glycosylated hemoglobin and the risk level of foot ulcers was positive.
实验室指标中血红蛋白、血小板计数、白蛋白、血沉以及电解质都有较高的异常率。
The process of extra-intestine isn't common. HB, PLT, ESR, ALB as well as dielectric have higher abnormality.
前者表现为血红蛋白分子的珠蛋白肽链结构异常，如镰刀状贫血；
The former is categorized by globin structural abnormality, like sickle cell disease;
前者表现为血红蛋白分子的珠蛋白肽链结构异常，如镰刀状贫血；
The former is categorized by globin structural abnormality, like sickle cell disease;
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