These morphologic changes provide basis for formation of idiopathic pulmonary fibrosis.

上述形态学改变对特发性肺纤维化的形成提供了一些依据.

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Idiopathic pulmonary fibrosis: acting or waiting?

特发性肺纤维化: 治疗还是等待?

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Objective To observe ultrastructural changes and study the pathogenesis of idiopathic pulmonary fibrosis.

目的观察特发性肺纤维化的超微结构变化并探讨其发病机理.

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Abstract: Objective To observe ultrastructural changes and study the pathogenesis of idiopathic pulmonary fibrosis.

文摘: 目的观察特发性肺纤维化的超微结构变化并探讨其发病机理.

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Background Bloemycin ( BLM ) induced pulmonary fibrosis ( BPF ) is most widely used animal model for idiopathic pulmonary fibrosis.

博莱霉素 ( BLM ) 所致的肺纤维化 ( BPF ) 模型是最常用的研究特发性肺纤维化的动物模型.

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Idiopathic pulmonary fibrosis ( IPF ) has a poor prognosis and a course that is unpredictable.

特 发性 肺纤维化预后不佳,其发展过程无法预知.

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Conclusions Mutations in the genes encoding telomerase components can appear as familial idiopathic pulmonary fibrosis.

结论:端粒酶组分的编码基因发生突变时,能以家庭性特发性肺纤维变性的形式出现.

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