hemoglobinuria

The evolution of paroxysmal nocturnal hemoglobinuria ( PNH) clone has been found very important in the pathogenesis of paroxysmal nocturnal haemoglobinuria.

随着阵发性睡眠性血红蛋白尿（PNH）发病机制研究的深入，很多学者都发现PNH细胞克隆的演变与疾病进展密切相关，可能是PNH发病的关键环节。

Paroxysmal nocturnal hemoglobinuria often goes unrecognized-its diagnosis may be delayed for more than 10 years.

该病往往难以发现,诊断延误可达十多年之久.

Objective : To study the effect of T-lymphocytes on hematopoietic progenitors in patients with paroxysmal hemoglobinuria ( PNH ).

目的: 研究阵发性睡眠性血红蛋白尿症 ( PNH ) 患者的 T 淋巴细胞对造血祖细胞的影响.

Although the dark urine may simply reflect dehydration, it could also reflect bilirubinuria or hemoglobinuria.

虽然黑尿可以简单地归因于脱水, 但是也可以归因于胆红素尿或血红蛋白尿.

OBJECTIVE: Paroxysmal nocturnal hemoglobinuria ( PNH ) is an acquired disease of the pluripotent hematopoitec stem cell.

[目的]阵发性睡眠性血红蛋白尿症 ( PNH ) 系后天获得性干细胞克隆性异常,临床表现为间断溶血、静脉血栓及不同程度的骨髓衰竭.

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。

hemoglobinuria, pnh hemolytic anemia of newborn

新生儿溶血性贫血

Objective To investigate the relationship between CD 59 and traditional hemolysis tests for paroxysmal nocturnal hemoglobinuria.

目的研究CD59抗原与传统的阵发性睡眠性血红蛋白尿症溶血试验之间的关系.