Idiopathic pulmonary fibrosis prognosis? Specific we look at.
特发性肺纤维化预后怎么样？具体的我们来看下。
The most likely diagnosis is Idiopathic pulmonary fibrosis (IPF).
最可能的诊断是特发性肺纤维化（IPF）。
Idiopathic Pulmonary Fibrosis; Lung paralysis; TCM clinical study.
特发性肺纤维化；肺痿；中医临床研究。
Idiopathic pulmonary fibrosis of common symptom is a cough, sputum, say the cause of idiopathic pulmonary fibrosis.
特发性肺纤维化的常见症状是咳嗽、咳痰，来说说特发性肺纤维化的病因。
Similar to the silicosis, idiopathic pulmonary fibrosis (IPF), which is another lung interstitial disease, is characterized by lung fibrosis.
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。
Objective To highlight the characteristics of Idiopathic pulmonary fibrosis(IPF) with marked elevated serum carbohydrate antigen sialyl Lewis(a)(CA19-9).
目的提高对CA19 9显著升高的特发性肺纤维化（IPF）的认识，评价CA19 9的升高与IPF进展的相关性。
The most common pattern seen on HRCT in patients with drug induced lung injury is that of fibrosis, indistinguishable from the appearance of idiopathic pulmonary fibrosis.
最常见的药物性肺损伤表现是肺纤维化，这不足以与特发性肺纤维化鉴别。
Recent research progress and therapeutic condition of Idiopathic Pulmonary Interstitial Fibrosis(IPIF) were reviewed.
就近来对特发性肺间质纤维化的研究进展及治疗现状进行分析。
Recent research progress and therapeutic condition of Idiopathic Pulmonary Interstitial Fibrosis(IPIF) were reviewed.
就近来对特发性肺间质纤维化的研究进展及治疗现状进行分析。
应用推荐