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1·The most likely diagnosis is Idiopathic pulmonary fibrosis (IPF).

最可能的诊断是特发性肺纤维化（IPF）。

2·XE-5000 is a practical and valid device for the detection of IPF.

XE-5000全自动血液分析仪是一种实用和有效的IPF检测仪器。

3·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。

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

随着流速的增大，流动阻力都呈现出增大的趋势。

5·The most notable characteristic feature of IPF is presence of fibroblastic foci.

IPF最显著的病理特征是成纤维细胞灶的存在。

6·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。

7·Methods The serum level of MMP-9 in 40 patients with IPF and 30 healthy subjects was measured by ELISA.

方法采用酶联免疫吸附法对40例特发性肺纤维化患者和30例健康人血清基质金属蛋白酶- 9进行测定。

8·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。

9·Conclusion Endogenous H2S was probably involved in the course of IPF, and was associated with the progress of the disease.

结论内源性H2S可能参与了IPF的疾病过程，可能与疾病的严重程度相关。

10·Conclusion: the IPF has characteristics on clinic and HRCT, and is different from interstitial lung disease with other causes.

结论：IPF在临床及HRCT表现上有其特点，有别于继发性肺间质性病变。