1)  IPF
IPF
1.
Objective To evaluate the relationship between idiopathic pulmonary fibrosis(IPF)patients and the level of cAMP and cGMP in the peripheral blood of IPF patients,and to find the functional status of glucocorticoid receptor of IPF patients,then to provide the experimental foundation of the application of cAMP for curing IPF.
目的检测特发性肺纤维化(IPF)患者外周血液中环核苷酸:环磷酸腺苷(cAMP)、环磷酸鸟苷(cGMP)的水平,探讨其与IPF的关系,以间接了解IPF患者糖皮质激素受体功能状态,并为cAMP在IPF治疗中的临床应用提供依据。
2.
Idiopathic Pulmonary Fibrosis (IPF) is a pulmonary disease belonging to Idiopathic Interstitial Pneumonia (IIP) and which patho-manifestation is Usual Interstitial Pneumonia (UIP).
特发性肺纤维化(idiopathic pulmonary fibrosis,IPF)系指特发性间质性肺炎(idiopathic interstitial pneumonia,IIP)中病理表现为普通型间质性肺炎(usual interstitial pneumonia, UIP)的一种类型,是IIP中最常见的一种,占47%-71%。
2)  IPF
特发性肺纤维化
1.
THE EXPRESSION AND CLINICAL SIGNIFICANCE OF SIGNAL TRANSDUCER AND ACTIVATOR OF TRANSCRIPTION 1 (STAT_1) IN LUNG TISSUE OF IDIOPATHIC PULMONARY FIBROSIS (IPF);
特发性肺纤维化肺组织STAT_1的表达及其临床意义
2.
To Study Effects and Feasibility of Life Quality List for IPF Patients;
特发性肺纤维化患者生存质量评价研究
3.
Objective To evaluate the relationship between idiopathic pulmonary fibrosis (IPF) patients and the level of cAMP and cGMP in the peripheral blood of IPF patients, and to find the functional status of glucocorticoid receptor of IPF patients, then to provide the experimental foundation of the application of cAMP for curing IPF.
在呼吸系统疾病方面,环核苷酸与哮喘、肺癌、慢阻肺、肺心病的相关性研究较多,但对特发性肺纤维化(IPF) 的研究却未见报道。
3)  IPF
含冰率
1.
The results show that the mixed liquor of sodium dodecyl sulfate & glycerin is the best additive for making ice slurry based on the liquidity of ice slurry,ice percent factor(IPF),and whether HCFC123 ca.
提出了喷射载冷剂HCFC123动态制冰的基本原理和制取冰浆的方法,分析了乙二醇、Tween-80、十二烷基硫酸钠及十二烷基硫酸钠+丙三醇复配溶液等4种添加剂在制取冰浆过程中的特点,以冰浆的流动性、含冰率(IPF)、HCHFC123能否从冰浆和含添加剂的溶液中析出作为判断依据,找到了十二烷基硫酸钠和丙三醇复配溶液是制取冰浆的最佳添加剂。
4)  IPF
Itanium处理器系统
5)  IPF algorithm
IPF算法
6)  idiopathic pulmonary fibrosis(IPF)
特发性肺纤维化
1.
Objective:To investigate the expression and significances of connective tissue growth factor in fibrotic lung tissue of patients with idiopathic pulmonary fibrosis(IPF).
目的:研究结缔组织生长因子(CTGF)在特发性肺纤维化(IPF)患者肺组织的表达及意义。
2.
Objective: To Study the effects and feasibility of life quality list for idiopathic pulmonary fibrosis(IPF) patients.
目的:探讨研究特发性肺纤维化患者的生存质量评价体系,评估生存质量测评表对特发性肺纤维化患者评价的可行性。
参考词条
补充资料：特发性纤维化肺泡炎


特发性纤维化肺泡炎
idiopathic fibrosing alveolitis

又称Hamman-Kich综合征。是一种原因不明的弥漫性进行性肺纤维间质化状态，可能不是一种疾病，而是多种原因所致的慢性间质性肺炎之终末阶段。临床起病多隐匿，以干咳、气短、进行性呼吸困难及发绀为主，一般不发热，肺活量减低，肺X线各期依次出现弥漫网点状阴影、粗条索阴影及蜂窝状肺。现无特殊疗法，预后不良。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。