The most likely diagnosis is Idiopathic pulmonary fibrosis (IPF).
最可能的诊断是特发性肺纤维化（IPF）。
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。
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。
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。
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。
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。
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。
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。
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。
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。
Results The serum levels of MMP-9 in IPF were significantly higher than that of healthy control, with significant difference (P<0.01).
结果患者血清基质金属蛋白酶-9水平高于健康对照组，差异有显著性意义（P<0.01）；
Similar to the silicosis, idiopathic pulmonary fibrosis (IPF), which is another lung interstitial disease, is characterized by lung fibrosis.
与矽肺的发病相似，特发性肺纤维化(IPF)也是以肺成纤维细胞大量增殖为主要特征的肺纤维化疾病。
Both Provident Financial and IPF collect loan payments from borrowers' homes each week, giving them instant information if a customer is struggling.
每周，远景金融和国际个人金融(IPF)公司的职员会到次贷者家中，收取还款。这样，一旦某个客户出现还款困难，他们就会立刻知道。
Enhanced Search provides a sample ipf file called ipfcsnclientconfig.xml (located in the configuration folder) which by default produces some basic logging.
EnhancedSearch提供名为ipfcsnclientconfig . xml(位于配置文件夹中)的示例ipf文件，其在默认情况下产生一些基本日志。
Objective To highlight the characteristics of Idiopathic pulmonary fibrosis(IPF) with marked elevated serum carbohydrate antigen sialyl Lewis(a)(CA19-9).
目的提高对CA19 9显著升高的特发性肺纤维化（IPF）的认识，评价CA19 9的升高与IPF进展的相关性。
The results showed that the main manifestations of IPF were severe dry cough, progressive short breath, cyanosis, clubbed fingers and crepitant rales in lungs.
结果发现，IPF主要表现为剧烈干咳、进行性气短、紫绀、杵状指趾和肺部捻发音。
Conclusions ET1 might play an important role in pathogenic of the patients with sarcoidosis and IPF. The levels of ET1 can act as the markers of activity of disease.
结论ET1在肺结节病和IPF发病机制中起着重要作用，并可作为疾病活动性判定的一项重要参考指标。
Most collagen-vascular diseases can cause chronic interstitial pneumonia with clinical, radiologic, HRCT, and pathologic features indistinguishable from those of IPF.
大部分胶原血管病在临床上会出现慢性间质性肺炎，无论平片、HRCT还是病理均无法于IPF鉴别。
The appeal of pulmonary hypertension in IPF is that it may be an enticing therapeutic target in a disease that otherwise does not have any proven effective therapies.
之所以重视IPF患者的肺动脉高压，是因为肺动脉高压可以成为治疗靶向，而除此之外IPF尚没有证明有效的治疗方法。
Meanwhile, given the weak accuracy of LS algorithm, IPF-LS and IDF-LS are proposed which can enhance the accuracy of channel estimation by employing time-domain low-pass filter.
同时，针对梳状导频ls信道估计精度较低的情况，提出了通过时域低通滤波提高其估计精度的IPF -LS和IDF - LS改进算法。
Conclusion IPF in peripheral blood can reflect the amount of platelets produced by megakaryocytes, thus contributing to the diagnosis and differential diagnosis of hematological diseases.
结论 外周血网织血小板数量可反映骨髓巨核系统生成血小板的情况，从而用于疾病的诊断和鉴别诊断。
Methods: Applying the self-made life quality evaluating list, life qualities of 36 cases of IPF patients were analyzed and compared before and after the intervention of traditional Chinese medicine.
方法：应用自制的生存质量测评表对36例特发性肺纤维化患者中医药干预前后的生存质量进行分析比较。
Methods: Applying the self-made life quality evaluating list, life qualities of 36 cases of IPF patients were analyzed and compared before and after the intervention of traditional Chinese medicine.
方法：应用自制的生存质量测评表对36例特发性肺纤维化患者中医药干预前后的生存质量进行分析比较。
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