1) Idiopathic pulmonary fibrosis(IPF)
特发性肺间质纤维化(IPF)
2) Idiopathic Pulmonary Fibrosis
特发性肺间质纤维化
1.
Review on Recent Therapeutic Condition and Progress of Idiopathic Pulmonary Fibrosis;
特发性肺间质纤维化的治疗现状与进展
2.
Detection and significance of serum cytokines levels in patients with idiopathic pulmonary fibrosis;
特发性肺间质纤维化患者血清细胞因子的检测及其意义
3.
Treatment of idiopathic pulmonary fibrosis with Qihong Decoction;
芪红汤治疗特发性肺间质纤维化的临床研究
3) idiopathic pulmonary interstitial fibrosis
特发性肺间质纤维化
1.
Effects of sodium ferulate on oxidative stress and pulmonary function of idiopathic pulmonary interstitial fibrosis patients;
阿魏酸钠对特发性肺间质纤维化患者氧化应激及肺功能的影响
2.
Objective:To study the effect of rehmannia (RM) on expression of transforming growth factor β-receptor type I (TGF-βR I) in idiopathic pulmonary interstitial fibrosis (IPIF).
目的:研究生地干预对特发性肺间质纤维化中转化生长因子β受体Ⅰ(TGF-βRⅠ)表达的影响。
4) Idiopathic pulmonary fibrosis
特发性肺纤维化
1.
Determination of T lymphocytes subset and cytokine of Th1/Th2 lymphocytes in peripheral blood mononuclear cells from patients with idiopathic pulmonary fibrosis;
特发性肺纤维化患者外周血单个核细胞T淋巴细胞亚群及Th1/Th2型细胞因子的检测
2.
Effect of cells in bronchoalveolar lavage on pulmonary function in idiopathic pulmonary fibrosis;
特发性肺纤维化支气管肺泡灌洗液细胞对肺功能的影响
3.
Correlation between cells obtained by bronchoalveolar lavage and pulmonary function in idiopathic pulmonary fibrosis;
特发性肺纤维化患者支气管肺泡灌洗液细胞对肺功能的影响(英文)
5) 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。
6) 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。
补充资料：弥漫性肺间质纤维化
弥漫性肺间质纤维化
，多种病因引起的以肺泡结构内的细胞及结缔组织基质发生紊乱，早期均表现为肺泡炎晚期为肺间质纤维化的一组异型的疾病。病变主要发生于肺间质、肺泡上皮、肺毛细血管内皮细胞和肺动、静脉。病种约有130个之多。其分类尚未统一，近年来倾向于将本病分为病因已明和病因未明二类，病因已明的如吸入各种粉尘、反复感染(病毒、细菌、真菌等），吸入气体(二氧化硫、氯、氧气等），所致的弥漫性间质性肺纤维化，原因未明的如隐原性致纤维性肺泡炎、肺纤维化伴发胶原-血管性疾病，肺出血-肾炎综合征等。由于肺间质纤维组织大量增生及肺泡弹性减弱，导致肺容量减少，限制性通气障碍、低氧血症等。临床症状以进行性气短、发绀及呼吸困难为主。X线检查可见弥漫网点状阴影及粗索条状阴影等。本病无特殊治疗，预后不佳。
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参考词条