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

1、

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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2、

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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4、

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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5、

molecular mechanism of activation of microglial cell

小胶质细胞激活的分子机制

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6、

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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7、

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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8、

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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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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10、

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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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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12、

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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13、

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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14、

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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15、

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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16、

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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17、

validity of names and nomenclatural acts

名称的有效

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18、

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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19、

nomenclatural relating to a system of names.

命名的与命名法有关的。

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20、

the work in which a name or nomenclatural act was first published . ( 2 ) of a name or nomenclatural act : publication for the first time.

含有首次发表的名称或命名举动的著作物。（2）一名称或命名举动：首次发表者。

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