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fibrotic相关的网络例句

查询词典 fibrotic

与 fibrotic 相关的网络例句 [注:此内容来源于网络,仅供参考]

Objective To investigate the effects of Qing Gan Yin on collagen fibers and reticular fibers in hepatic fibrotic rats.

目的 研究中药清肝饮对大鼠肝纤维化模型胶原纤维和网状纤维的影响。

RESULTS: HSC were mostly detected close to areas of lobular necroinflammation or lining fibrotic septa.

结果:肝星状细胞与肝小叶炎症损伤区或内壁纤维化区接近。

SPARC (secreted protein, acidic and rich in cysteine) is a key determinant of progressive fibrotic diseases.

富含半胱氨酸的酸性分泌糖蛋白是纤维化疾病进程中的一个关键因素。

Splenomegaly is the leading factor of peripheral blood cells decrease in patients with chronic hepatitis, and blood platelet count is valuable for predicting fibrotic degree.

脾脏增大是慢性肝炎外周血细胞计数减少的主要原因,血小板计数有预测肝纤维化程度的价值。

Esophageal motility problems can occur in patients with progressive systemic sclerosis because the submucosa becomes fibrotic .

在进行性系统性硬化症的患者可以发生食管黏膜蠕动减弱的问题,是由于黏膜下层的组织发生了纤维化。

One of most possible cause of sudden death may be fibrotic quiver of left ventricle.

猝死的常见的原因是心脏的左心室发生了无规则的纤维性颤动。

From June 2002 to March 2003, 29 men with obliterative strictures of the bulbomembranous urethra underwent the core-through procedure. The length of the stricture was 2.5 cm or shorter in all patients, with good alignment between the two urethral ends. The obliterative fibrotic tissue was vaporized by a holmium laser guided by a metal sound introduced through the suprapubic tract.

从2002年6月到20033月,29位球膜尿道的闭锁性尿道狭窄的男性接受穿越核心的外科手术,所有患者的狭窄部位长度为2.5公分或小于2.5公分,其手术部位尿道两端的精准度相当好,闭锁纤维化组织藉由钬雷射的金属探针经由上耻骨通道被蒸发。

From June 2002 to March 2003, 29 men with obliterative strictures of the bulbomembranous urethra underwent the core-through procedure. The length of the stricture was 2.5 cm or shorter in all patients, with good alignment between the two urethral ends. The obliterative fibrotic tissue was vaporized by a holmium laser guided by a metal sound introduced through the suprapubic tract.

从2002年6月到20033月,29位球膜尿道的闭锁性尿道狭窄的男性接受穿越核心的外科手术,所有患者的狭窄部位长度为2.5公分或小於2.5公分,其手术部位尿道两端的精准度相当好,闭锁纤维化组织藉由钬雷射的金属探针经由上耻骨通道被蒸发。

Congenital fibrosis syndrome is a rare familial hereditary disease, characterized by fibrotic change of extraocular muscles.

摘要先天性纤维化症候群是一少见的家族性遗传疾病。

It is closely related to the occurrence and progress of fibrotic diseases.

这些功能同纤维化的发生、发展密切相关。

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