idiopathic pulmonary fibrosis, which has no known cause, affects 70,000 to 200,000 americans, according to various estimates.

1、

pfd was used as multi-target drug and was approved in japan for the treatment of idiopathic pulmonary fibrosis.

该药物于2008年11月在日本上市，用于治疗特发性肺纤维化。

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2、

changes of cyclic nucleotides and nitric oxide in the plasma of patients with idiopathic pulmonary fibrosis

特发性肺纤维化患者血浆环核苷酸和一氧化氮水平研究

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3、

experimental imaging studies of early-stage idiopathic pulmonary fibrosis-animal model and preliminary results

实验性特发性肺纤维化的早期影像研究&动物模型的建立

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4、

study on the treatment of idiopathic pulmonary fibrosis with prednisone, n-acetylcysteine combined captopril

强的松、N-乙酰半胱氨酸和卡托普利联合治疗特发性肺纤维化

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diagnostic value of left ventricular geometry and function by echocardiography in idiopathic pulmonary fibrosis

特发性肺纤维化左心构型及功能的超声心动图诊断价值初探

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6、

idiopathic pulmonary fibrosis; tumor biomarkers; prognosis;

特发性肺纤维化；肿瘤标志物；预后；

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effects of bcg-psn combined with glucocorticoid on patients with idiopathic pulmonary fibrosis

卡介菌多糖核酸与糖皮质激素联合应用对特发性肺纤维化的抑制作用

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the measurement of glutathione in bronchoalveolar lavage fluid with idiopathic pulmonary fibrosis

特发性肺纤维化患者支气管肺泡灌洗液谷胱甘肽的检测

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lung function tests and corticosteroid therapy in idiopathic pulmonary fibrosis

特发性肺纤维化肺功能测定与激素治疗

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bone marrow derived stem cells for idiopathic fibrosis of the lung

骨髓源干细胞与特发性肺纤维化的治疗

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expression of type ⅲ collagen in bleomycin-induced pulmonary fibrosis

Ⅲ型胶原纤维在实验性特发性肺纤维化早期的动态研究

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12、

backgrounds: idiopathic pulmonary fibrosis ( ipf) is a progressive lung disorder of unknown etiology. the disease is characterized by aberrant proliferation of fibroblasts and finally by formation of scar tissues with the subsequent destruction of the lung architecture.

研究背景：特发性肺纤维化（IPF）是一种以肺内成纤维细胞不明原因的异常增殖形成瘢痕组织为主要特征的进行性肺部纤维化疾病，其病理机制目前还不清楚。

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13、

we compared the effect of intermittent, intravenous cyclophosphamide ( ctx) and low dose prednisone ( c ± p) in 16 patients with idiopathic pulmonary fibrosis ( ipf) with that of high dose prednisone alone ( p) in 18 cases of iff.

以大剂量强的松（P组）治疗18例特发性肺纤维化（IPF）作为对照，与间断静脉滴注环磷酰胺（CTX）加小剂量强的松（C+P）组治疗的16例IPF患者进行了对比观察。

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14、

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。

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15、

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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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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17、

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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18、

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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19、

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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20、

molecular mechanism of activation of microglial cell

小胶质细胞激活的分子机制

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