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Idiopathic pulmonary fibrosis Idiopathic pulmonary fibrosis ( IPF ), formerly known as cryptogenic fibrosing alveolitis , [5] is a rare, progressive illness of the respiratory system, characterized by the thickening and stiffening of lung tissue, that surrounds the air sacs, and is associated with the formation of scar tissue

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Effects on congestive heart failure-associated myopathy may be due to caspase inhibition and decreased TNF-alpha levels (14)

VPA-exposed rats (Fig

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