Topological data analysis identifies molecular phenotypes of idiopathic pulmonary fibrosis

BACKGROUND: Idiopathic pulmonary fibrosis (IPF) is a debilitating, progressive disease with a median survival time of 3–5 years. Diagnosis remains challenging and disease progression varies greatly, suggesting the possibility of distinct subphenotypes. METHODS AND RESULTS: We analysed publicly avail...

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Detalles Bibliográficos
Autores principales: Shapanis, Andrew, Jones, Mark G, Schofield, James, Skipp, Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2023
Materias:
Interstitial Lung Disease
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10314053/
https://www.ncbi.nlm.nih.gov/pubmed/36808085
http://dx.doi.org/10.1136/thorax-2022-219731

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10314053/
https://www.ncbi.nlm.nih.gov/pubmed/36808085
http://dx.doi.org/10.1136/thorax-2022-219731

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