ipf

Idiopathic pulmonary fibrosis ( IPF ) has a poor prognosis and a course that is unpredictable.

特 发性 肺纤维化预后不佳,其发展过程无法预知.

Although the modern medicine research has reached certain progress on IPF therapy, there is no ideal therapy drug for IPF.

随着现代医学的深入研究，特发性肺间质纤维化在治疗上有了一定的进展，但目前尚没有理想的治疗药物。

Results IPF algorithm could effectively fit the model for high way table and give a reasonable interpretation.

结果IPF算法能够很好地拟合高维表的模型，并得出了合理的结果。

There are multiple factors that might influence the onset and severity of pulmonary hypertension in IPF.

有很多因素可影响IPF过程中肺动脉高压的出现和严重度。

This paper discussed the IPF algorithm in practical aspect.

本文从应用角度探讨了IPF算法的有效性。

When the IPF increases, the flow resistance of the ice slurry became larger.

随着IPF的增大，二元冰的摩擦阻力变大。

To Study Effects and Feasibility of Life Quality List for IPF Patients

特发性肺纤维化患者生存质量评价研究

HRCT and cardiorespiratory exercise test could significantly raise the early diagnostic level of IPF.

HRCT与运动心肺功能试验联合检查能显著提高IPF的早期诊断水平。

Results: The evaluating list of life quality is available for IPF patients.

结果：本生存质量测评表能够有效地评价特发性肺纤维化患者的生存质量；

IPF Patients with Low-molecular-weight Heparin on Serum HGF Expression and Clinical Efficacy Study

低分子肝素钠对IPF患者血清中HGF表达的影响及临床疗效的研究

These results indicate the usefulness of lung function tests in the diagnosis of IPF and the value of corticosteroid therapy.

初步结论；肺功能检测对辅助诊断特发性肺纤维化和评价激素疗效，均有重要的临床价值。

Conclusions DcR 3 gene of PBMC over express in patients with IPF.

结论　IPF病人PBMC中DcR3基因的表达水平增高.

Objective: To Study the effects and feasibility of life quality list for idiopathic pulmonary fibrosis ( IPF) patients.

目的：探讨研究特发性肺纤维化患者的生存质量评价体系，评估生存质量测评表对特发性肺纤维化患者评价的可行性。

Methods An example of 5 way table was Analyzed using IPF algorithm.

方法采用IPF算法对一个五维表进行了分析。

IPF is characterized by progressive injury, inflammation, and fibrosis of the lung parenchyma.

特发性肺纤维化以进行性肺损伤、炎症、肺组织纤维化为特征。

Objective To evaluate the value of DR post process in diagnosis of IPF.

目的分析胸片DR后处理功能在特发性肺间质纤维化（IPF）诊断中的作用。

This article introduce some approaches that can learn speciation distribution of IPF of Fe, and some research of this field.

本文着重介绍了铁系絮凝剂中铁的形态分布的分析方法的发展。

Chapter 6 is about the study on the contract law system in IPF.

第八章主要研究国际项目融资有关的税法问题。

IPF clinical situation includes progressive dyspnea, dry cough and restrictive ventilatory disorder.

临床表现为进行性呼吸困难伴有刺激性干咳，肺功能为限制性通气障碍。

Correlation Between Curative Effect of Gingko Flavonoid Glycosides on IPF and Immune Cytokines

银杏黄酮甙治疗肺间质纤维化疗效与免疫细胞因子相关性研究

Analysing ultrastructure characteristic in the ruthenium red staining on the rats with IPF

钌红染色对大鼠特发性肺间质纤维化的超微结构分析

The early diagnostic value of cardiopulmonary exercise test in IPF

运动心肺功能试验对特发性肺纤维化早期诊断价值探讨

In the pulmonary tissue of patients with IPF, we observed the same as above.

IPF患者肺组织中也观察到同样的结果。

IPF Algorithm of Log-linear Model and Software Implement

对数线性模型的IPF算法及其软件实现

HRCT and exercise test could significantly raise the early diagnostic level of IPF.

HRCT与运动心肺功能试验联合检查能显著提高IPF的 早期诊断水平.

The literature about diagnosis and correlative study on IPF is reviewed.

现结合有关文献对特发性肺纤维化的诊断和相关研究作一综述。

Charge characteristics and infrared spectra of polymeric phosphate ferric sulfate of IPF

无机高分子絮凝剂聚磷硫酸铁的带电特征与红外光谱分析

The Treatment Mechanism of Cell Apoptosis of Yiqi Tongluo Decoction on IPF Fibrosis Phase

益气通络解毒方治疗IPF的细胞凋亡机制

One IPF case was complicated with lung cancer.

1例为IPF合并肺癌。

The adding of Si can enhance the structure ordering in IPF.

在TX203絮凝剂中Si有增强结构序性的作用。