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- secondary pulmonary fibrosis 肺纤维化
- Quercetin could prevent and treat BLM induced pulmonary fibrosis. 槲皮素对博莱霉素致肺纤维化有一定的防治作用
- Pulmonary fibrosis is an important toxic effect of paraquat. 在各种肺组织损伤中又以肺纤维化损伤最为突出。
- The most likely diagnosis is Idiopathic pulmonary fibrosis (IPF). 最可能的诊断是特发性肺纤维化(IPF)。
- Only about 1% of such persons get a significant degree of pulmonary fibrosis. 仅有大约1%25的这种病人出现明显的肺纤维化。
- Objective: Acute idiopathic pulmonary fibrosis (AIPF) is a rare disease. 目的:急性特发性肺间质纤维化是少见疾病。
- secondary diffuse interstitial pulmonary fibrosis 继发性弥漫性肺间质纤维化
- Taking little dose fluconazole orally for preventing the secondary pulmonary fungal infection in patients with PHD is effect and safe. 小剂量(100mg)氟康唑口服预防肺心病住院患者继发肺部真菌感染,疗效确切,使用安全。
- Methods Ninety-eight cases of secondary pulmonary tuberculosis and hematogenous disseminated pulmonary tuberculosis were clinically analyzed. 方法对98例确诊为继发型肺结核和血行播散型肺结核患者,统计分析痰液及纤支镜刷检液涂片抗酸染色情况。
- The results indicate that rat model of pulmonary fibrosis replicated by BLM is similar to that of mankind. 结果表明:博莱霉素肺纤维化动物模型的肺病理组织学与病理生理学改变与人肺纤维化相似。
- Improements in right heart hemodynamics and exercise capacity were confined to patients with secondary pulmonary hypertension (rest pulmonary arterial pressure >25 mm Hg). 患有继发性肺动脉高压(静息时肺动脉压>25mmHg)的患者,其右心血流动力学以及运动量的改善受到限制。
- It was similar to the two groups in late reaction to radioactive pulmonary fibrosis. 在减轻放射性肺纤维化等晚反应方面两组相似。
- These morphologic changes provide basis for formation of idiopathic pulmonary fibrosis. 上述形态学改变对特发性肺纤维化的形成提供了一些依据。
- 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枯所致肺纤维化发生机制的研究进展进行综述。
- Objective To evaluate the effect of dipyridamole (DPM) and adenosine(ADO) on interstitial pulmonary fibrosis in mice. 目的 通过腺苷 (ADO)受体拮抗剂 茶碱 (TH) ,探讨ADO、双哌达莫 (DPM)对小鼠肺间质纤维化过程的干预作用。
- Objective To observe ultrastructural changes and study the pathogenesis of idiopathic pulmonary fibrosis. 目的观察特发性肺纤维化的超微结构变化并探讨其发病机理。
- To determine the visibility of the normal secondary pulmonary lobule on HRCT scans,the HRCT images of three fresh cadavers thorax were correlated with gross and histologic cross-sectional anatomy of the lung. 为了明确正常肺小叶HRCT表现,本文仅将标本处理前的HRCT像与相应的横断大体标本、组织学切片行对照观察。
- Objective To study the role of matrix metalloproteinase-2 (MMP 2) in rat pulmonary fibrosis. 目的 研究基质金属蛋白酶 2 (MMP2 )在肺纤维化中的作用。
- Only patients with secondary pulmonary hypertension, defined as a resting pulmonary arterial pressure of more than 25 mmHg, demonstrated improements in right heart hemodynamics and exercise capacity. 而继发性肺动脉高压患者(静息时肺动脉压>25mmHg)右心血流动力学和运动耐量的改善受到限制。
- Diagnosis: Idiopathic pulmonary fibrosis, with intralobular interstitial thickening. 诊断:特发性肺纤维化并小叶间质增厚。