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There is detectable variation in the lipidomic profile between stable and progressive patients with idiopathic pulmonary fibrosis (IPF)

BACKGROUND: Idiopathic pulmonary fibrosis (IPF) is a chronic interstitial lung disease characterized by fibrosis and progressive loss of lung function. The pathophysiological pathways involved in IPF are not well understood. Abnormal lipid metabolism has been described in various other chronic lung...

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Detalhes bibliográficos
Publicado no:Respir Res
Main Authors: Nambiar, Shabarinath, Clynick, Britt, How, Bong S., King, Adam, Walters, E. Haydn, Goh, Nicole S., Corte, Tamera J., Trengove, Robert, Tan, Dino, Moodley, Yuben
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2021
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC8033725/
https://ncbi.nlm.nih.gov/pubmed/33836757
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12931-021-01682-3
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