• Results: The rat model of pulmonary fibrosis was established.

    结果大鼠实验性肺纤维化模型成功;

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  • Pulmonary fibrosis is difficult to cure and has a bad prognosis.

    纤维化治疗困难,预后

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  • Idiopathic Pulmonary Fibrosis; Lung paralysis; TCM clinical study.

    特发性纤维化中医临床研究

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  • So far, no pulmonary fibrosis a safe and effective therapeutic drugs.

    迄今为止,间质纤维化尚无一种安全有效治疗药物。

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  • Objective To study the roles of fibronectin played in rat pulmonary fibrosis.

    目的研究纤维连接蛋白纤维化中的作用

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  • Only about 1% of such persons get a significant degree of pulmonary fibrosis.

    仅有大约1%这种病人出现明显的纤维化。

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  • Objective: To study the relation of pulmonary fibrosis and bioactivity mediums.

    目的探讨矽肺纤维化生物活性介质之间关系

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  • Lung distortion, honeycomb cysts, traction bronchiectasis and pulmonary fibrosis.

    结构变形蜂窝状囊性变牵引性支扩纤维化。

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  • It was similar to the two groups in late reaction to radioactive pulmonary fibrosis.

    减轻放射性纤维化等晚反应方面相似

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  • Pulmonary fibrosis caused by respiratory and circulatory failure is the main cause of death.

    纤维化所致呼吸循环衰竭致死主要原因

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  • A trichrome stain highlights the collagenous connective tissue of pulmonary fibrosis in blue.

    三色染色把纤维化病人结缔组织中的胶原纤维染成蓝色。

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  • Method A single dose of BLM was intratracheally injected to induce pulmonary fibrosis of mice.

    方法小鼠气管内注入BLM复制纤维化模型。

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  • Pulmonary fibrosis is caused by many factors and shows diffuse interstitial tissue hyperplasia.

    纤维化多种原因导致的,以弥漫性肺间质组织增生为特征的疾病。

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  • Conclusion Lowere dose quartz has very strong toxicity to the lungs leading to pulmonary fibrosis.

    结论剂量石英具有很强毒性和致纤维化能力。

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  • By dust spot with focal weeks emphysema is given priority to, with mild diffuse pulmonary fibrosis.

    肺气肿为主,可轻度弥漫性纤维化

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  • Recent studies on the pathogenesis of paraquat-induced pulmonary fibrosis are reviewed in this paper.

    该文就近年来关于百草所致肺纤维化发生机制研究进展进行综述。

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  • The main histopathological changes were diffuse pulmonary fibrosis and deposition of large amount of dust.

    主要病变弥漫性纤维化,有纤维细胞结节形成

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  • All of this shows that scleroderma patients with pulmonary fibrosis than before treatment significantly improved.

    这些都表明硬皮病患者间质纤维化的程度较治疗明显好转。

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  • No pulmonary fibrosis, secondary malignancies and abnormity of growth and development were found during follow-up.

    随访期间发生纤维化继发肿瘤生长发育异常等不良事件。

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  • Diffuse interstitial pulmonary fibrosis was a group of diseases which had the similar morphology and different etiology.

    弥漫性肺间质纤维化病因各异,病理形态相似疾病

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  • The X-ray changes of 10 cases of pathologically proved cryptogenic diffuse interstitial pulmonary fibrosis are reported.

    本文报道活检证实10隐原性弥漫性肺间质纤维化X线改变

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  • AIM: To study the effect of Chinese medicine Feining on early experimental pulmonary fibrosis in rats induced by bleomycin.

    目的观察中药博莱霉素诱导大鼠纤维化早期的防治作用

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  • Objective to study the injury effect of ammonium perchlorate (AP) to lung and to explore whether AP can cause pulmonary fibrosis.

    目的研究过氯酸(AP)组织损害作用探讨AP有无纤维化作用

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  • The drug decreases the inflammation that causes pulmonary fibrosis and has been used on scleroderma patients for the last 10 years.

    该药使导致纤维化炎症得以减轻过去10年里应用硬皮病患者

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  • Objective: to observe the effect of inhaled budesonide on pulmonary fibrosis induced by bleomycin in rats and to explore its mechanism.

    目的观察雾化吸入布地奈德纤维化干预作用探讨作用机制

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  • Pulmonary fibrosis caused by the end of the respiratory and circulatory failure in patients with scleroderma is the main factor of death.

    间质纤维化最终引起呼吸循环衰竭硬皮病患者主要致死因素之一。

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  • AIM: To investigate the protective effect of Okam extract J201 on bleomycin induced pulmonary fibrosis in rats and the underlying mechanism.

    目的研究昆布提取物j201纤维化治疗作用及其可能作用机制。

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  • Objectives:To observe the effect of kangqian Granule in treating diffuse pulmonary fibrosis and the effect on extracellular matrix of serum.

    目的观察特发性间质纤维化患者血清细胞外基质成分改变中药抗纤颗粒影响

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  • Similar to the silicosis, idiopathic pulmonary fibrosis (IPF), which is another lung interstitial disease, is characterized by lung fibrosis.

    矽肺的发病相似,特发性纤维化(IPF)也是成纤维细胞大量增殖主要特征的肺纤维化疾病

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  • Objective: to study the formation of pulmonary fibrosis from morphological and functional aspects and to offer therapy for pulmonary fibrosis.

    前言:目的:形态学功能研究纤维化形成过程治疗肺纤维化提供依据。

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