Idiopathic pulmonary fibrosis.
By S. Rosselot. Nursing Standard, 2014
4,086 citations recorded by the source corpus.
Subfields: Pulmonary and Respiratory Medicine
View Paper: https://www.semanticscholar.org/paper/3d70780bd070209a4df59982b68de988438ede88
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In Pulmonary and Respiratory Medicine
Citations in the corpus
- Diagnostic criteria for idiopathic pulmonary fibrosis: a Fleischner Society White Paper. (2017, background): “The diagnostic criteria for IPF published in 2011(1) have been critical for defining entry criteria and ensuring appropriate recruitment for recent prospective clinical trials.(2-7) In turn, these trials, with large cohorts of well-”
- Long COVID or post-COVID-19 syndrome: putative pathophysiology, risk factors, and treatments (2021, background): “These studies collectively indicate that pulmonary scarring may be a common sequela of COVID-19, which may be responsible for persistent dyspnoea and cough in long COVID [66,67].”
- Targeting TGF-β signal transduction for fibrosis and cancer therapy (2022, background): “TGF-β is a key profibrotic factor in IPF, but inhibiting TGF-β causes multiple side effects due to its pleiotropic effects.”
- Wnt/β-catenin signalling: function, biological mechanisms, and therapeutic opportunities (2022, background): “IPF is a disease characterized by the progressive loss of lung function distinguished by severe pulmonary epithelial injury, fibroblast activation, extracellular matrix deposition, and distorted lung development.(93) In IPF, abnormally activated Wnt signalling is detected, which manifests as follows”
- Monocyte-derived alveolar macrophages drive lung fibrosis and persist in the lung over the life span (2017, background): “The decline in lung function in patients with fibrosis is not continuous, and step declines are often preceded by the development of “exacerbations,” or an acute or subacute clinical worsening of shortness of breath and hypoxemia accompanied by inflammatory infiltrates on computed tomography imaging”