Results 151 to 160 of about 182,666 (399)
Objectives Systemic sclerosis (SSc) is a connective tissue disease with fibrotic remodeling of the skin and various internal organs. SSc is associated with the highest case‐specific mortality of all rheumatic autoimmune diseases with limited antifibrotic treatment options.
Thuong Trinh‐Minh+12 more
wiley +1 more source
In the education component of pulmonary rehabilitation, people with bronchiectasis seek to obtain greater clarity on the underlying cause of their condition and its prognosis. Further knowledge about self‐management strategies, treatment for extra‐pulmonary symptoms and the role of exercise outside of pulmonary rehabilitation as part of management were
Annemarie L. Lee+12 more
wiley +1 more source
Consensus document for the diagnosis and treatment of idiopathic pulmonary fibrosis
Idiopathic pulmonary fibrosis is a rare interstitial lung disease included in the Idiopathic Interstitial Pneumonias group. Although several potential risk factors have been described, it is a progressive fibrosing disease of unknown cause affecting ...
C. Robalo Cordeiro+12 more
doaj
Joint Models for Time-to-Event Data and Longitudinal Biomarkers of High Dimension [PDF]
Joint models for longitudinal biomarkers and time-to-event data are widely used in longitudinal studies. Many joint modeling approaches have been proposed to deal with different types of longitudinal biomarkers and survival outcomes. However, most existing joint modeling methods cannot deal with a large number of longitudinal biomarkers simultaneously,
arxiv
Diffuse pulmonary hemosiderosis after exposure to pesticides - A case report [PDF]
This report describes the clinical, radiological, microscopical and ligandohistochemical findings in a 17-year-old woman who suffered from an acute onset of pulmonary hemosiderosis after inhalation of pesticides used for the cultivation of strawberries ...
Altiner, Mithat+5 more
core +1 more source
This review highlights the complex roles of cellular senescence in cancer progression and suppression, discusses the mechanisms and regulatory pathways involved, and evaluates the efficacy of the “One‐Two punch” sequential treatment approach while addressing emerging challenges in this novel therapeutic strategy.
Qiuming Pan+12 more
wiley +1 more source
99mTc-MIBI Lung Scintigraphy in the Assessment of Pulmonary Involvement in Interstitial Lung Disease and Its Comparison With Pulmonary Function Tests and High-Resolution Computed Tomography: A Preliminary Study [PDF]
The differentiation of active inflammatory processes from an inactive form of the disease is of great value in the management of interstitial lung disease (ILD).
Assadi, M.+6 more
core +2 more sources
The therapy of idiopathic pulmonary fibrosis: what is next?
Idiopathic pulmonary fibrosis (IPF) is a chronic, progressive, fibrosing interstitial lung disease, characterised by progressive scarring of the lung and associated with a high burden of disease and early death.
V. Somogyi+5 more
semanticscholar +1 more source
Prevalence of Cystic Fibrosis Carrier Status in Chronic Rhinosinusitis Without Nasal Polyp
International Forum of Allergy &Rhinology, EarlyView.
Do‐Yeon Cho+4 more
wiley +1 more source
Lamellarin D Acts as an Inhibitor of Type I Collagen Production
COL1A2 gene, encoding type I collagen, is a key target for pulmonary fibrosis. We established a screening system to identify small molecules that inhibit COL1A2 gene expression. Using this system, we screen a library of compounds and identify lamellarin D as a potent inhibitor of COL1A2 expression, suggesting lamellarin D is a promising new lung ...
Daisuke Okuno+19 more
wiley +1 more source