Results 191 to 200 of about 73,124 (298)
Identification of a conserved sequence of disease progression in Idiopathic Pulmonary Fibrosis. [PDF]
Huang X +6 more
europepmc +1 more source
Abstract Type 2 diabetes (T2D) is a major global health concern strongly associated with atherosclerosis and subsequent macrovascular complications. These complications are the leading cause of death among T2D patients. Despite a decline in cardiovascular events over the last decade, individuals with T2D still have an approximately doubled risk ...
Dania Al‐Sharify +2 more
wiley +1 more source
A systematic review of artificial intelligence-based diagnosis models for idiopathic pulmonary fibrosis. [PDF]
Yan RN +7 more
europepmc +1 more source
Breathomics is established as a non‐invasive diagnostic strategy by combining volatile organic compound biomarkers, nanomaterial‐based sensor arrays, and AI‐driven classification. Key diseases, sensing materials, and analytical challenges are critically compared, revealing how portable, data‐enabled breath platforms are moving toward clinically useful ...
Anesu Nyabadza +3 more
wiley +1 more source
Combined HDL-BMI Phenotyping Provides Incremental Prognostic Value in Idiopathic Pulmonary Fibrosis. [PDF]
Shen Q +6 more
europepmc +1 more source
In fibrotic distal lung regions, CD66c+ basal cells emerge as a pathological state. Using human distal lung organoids, this study identifies CD66c+ basal cells as a pro‐fibrotic state arising through transdifferentiation from secretory, AT2, and basal cells.
Kaijun Lin +13 more
wiley +1 more source
Phenotype-specific considerations in antifibrotic therapy for idiopathic pulmonary fibrosis: refining risk assessment. [PDF]
Ding X, Lv X.
europepmc +1 more source
Producing MSCs on rigid culture substrates induces a scar‐making phenotype, jeapordizing therapeutic success. ‘Tissue‐soft’ surfaces prevent MSC fibrogenesis and preserve regenerative traits. An epigenetic network, driven by HOXA11 and SALL1, maintains ‘soft memory’ by keeping chromatin open in relaxed MSCs, promoting anti‐fibrotic programs.
Fereshteh Sadat Younesi +7 more
wiley +1 more source
Unusual Presentation of Orofacial Granulomatosis Leading to the Incidental Diagnosis of Idiopathic Pulmonary Fibrosis: A Case Report. [PDF]
Mohammed F, Bentahar O.
europepmc +1 more source
Aim Clinically, interstitial lung disease (ILD) is a heterogeneous group of respiratory disorders. Due to their low incidence, pharmacovigilance database analysis is useful to detect them. Precise diagnosis is challenging as well as coding in these databases. Query criteria are among the key elements for a good signal detection.
Romane Freppel +4 more
wiley +1 more source

