Pulmonary fibrosis (PF) is characterised by several grades of chronic inflammation and
collagen deposition in the interalveolar space and is a hallmark of interstitial lung diseases …

Idiopathic pulmonary fibrosis (IPF) is a long-lasting, continuously advancing, and irrevocable
interstitial lung disorder with an obscure origin and inadequately comprehended …

Fibrosis is a pathological process associated with most chronic inflammatory diseases. It is
defined by an excessive deposition of extracellular matrix proteins and can affect nearly …

IPF is a fatal lung disease characterized by intensive remodeling of lung tissue leading to
respiratory failure. The remodeling in IPF lungs is largely characterized by uncontrolled …

Idiopathic pulmonary fibrosis (IPF), one of the most common fibrosing interstitial lung
diseases (ILD), is a chronic-age-related respiratory disease that rises from repeated micro …

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Background Idiopathic pulmonary fibrosis (IPF) is a progressive, deadly lung disease with
several factors, including respiratory tract infections (RTI), for disease worsening. There's no …

Idiopathic pulmonary fibrosis is a progressive and incurable lung disease characterized by
collagen deposition, alveolar inflammation, fibroblast proliferation, and the destruction of …

Rationale: Idiopathic pulmonary fibrosis (IPF) is a progressive fibrotic pulmonary disorder of
unknown etiology that is characterized by a usual interstitial pneumonia pattern. Previous …

Despite the tremendous advancements in the knowledge of the pathophysiology and clinical
aspects of SARS-CoV-2 infection, still many issues remain unanswered, especially in the …