similar to the silicosis, idiopathic pulmonary fibrosis ( ipf), which is another lung interstitial disease, is characterized by lung fibrosis.

1、

methods retrospective analysis was conducted on 48 cases of ipf according to the diagnostic criteria formulated by the ats/ ers.

方法对48例符合ATS/ERS提出的特发性肺纤维化诊断标准IPF患者进行回顾性分析。

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2、

idiopathic pulmonary fibrosis is clinically characterized by progressive dyspnea and is similar to shortness of breath described in tcm.

特发性肺纤维化（IPF）临床以进行性呼吸困难为特征，与中医所论短气相似。

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3、

high resolution ct evaluation of idiopathic pulmonary fibrosis

特发性肺纤维化的高分辨率CT评价

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idiopathic pulmonary fibrosis: correlation between helical ct features and clinical stage

特发性肺纤维化的螺旋CT表现特征与临床病程的相关性

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5、

protein c anticoagulant system in patients with idiopathic pulmonary fibrosis

特发性肺纤维化患者蛋白C系统的研究

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6、

molecular mechanism of activation of microglial cell

小胶质细胞激活的分子机制

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7、

technology and mechanism of activation for membrane electrode assembly in proton exchange membrane fuel cell

质子交换膜燃料电池膜电极活化工艺及机理

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8、

this effect by using a device made of a vacuum phototube, photomultiplier tubes.

利用这种效应所做成的器件有真空光电管、光电倍增管等。

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9、

mix the poppyseed-fix with other ingredients for the filling in a bowl.

混合馅料的所有原料在一个碗里备用。

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10、

pulmonary interstitial fibrosis is a kind of pulmonary interstitial disease which manifested by progressing dyspnea, asthma, short breath, dry cough and characterized by limiting ventilation perfusion ratio, hypoxemia, chronic progressing diffused pulmonary interstitial fibrosis.

肺间质纤维化是以进行性呼吸困难、喘息、气短、干咳、喘憋为临床表现、以限制性通气功能障碍、低氧血症、慢性进行性弥漫性肺间质纤维化为特点的肺间质性疾病。

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11、

objective: interstitial pulmonary fibrosis is a series of diseases characterized by early alveolus lesion, inflammatory cells infiltration, followed with collagen aggradation and finally changed into interstitial fibrosis.

目的：肺间质纤维化是一组早期有肺泡细胞损伤和各种炎性细胞浸润，继后出现胶原纤维沉积，并逐渐演变了弥漫性肺间质纤维化的疾病群。

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12、

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是一组病因各异，病理形态相似的疾病。

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13、

kangxian granule therapy in patients with diffuse pulmonary fibrosis and effect on cell factor

弥漫性肺间质纤维化细胞因子改变及抗纤颗粒的作用

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14、

diagnostic value of exercise diffusion capacity test on diffuse pulmonary fibrosis

运动弥散量测定对弥漫性肺间质纤维化的诊断价值

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15、

abstracts idiopathic diffusive pulmonary interstitial fibrosis: report of 13 cases

特发性弥漫性肺间质纤维化13例治疗报告

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16、

there were also 5 cases of pneumonia ( 76.7%), 3 cases of uremia pneumonedema ( 10%), 2 cases of diffuse pulmonary interstitial fibrosis ( 6.7%) and one case of atelectasis ( 3.3%).

其次为SLE肺炎5例（16.7%），尿毒症肺水肿3例（10%），弥漫性肺间质纤维化2例（6.7%），肺不张1例（3.35%）。

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17、

one hundred thirty-nine cases of diffuse interstitial fibrosis of lung were pre-sented, 34 cases of them being idiopathic pulmonary fibrosis.

本文报告139例弥漫性肺纤维化，内含34例特发性纤维化。

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18、

validity of names and nomenclatural acts

名称的有效

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19、

of an available name or a nomenclatural act: one that is not valid under the code.

一适用名称或命名举动：依本规约的规定为无效者。

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20、

nomenclatural relating to a system of names.

命名的与命名法有关的。

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