Intermittent chylomicronemia caused by intermittent GPIHBP1 autoantibodies

Chylomicronemia caused by a deficiency in lipoprotein lipase (LPL) or GPIHBP1 (the endothelial cell protein that transports LPL to the capillary lumen) is typically diagnosed during childhood and represents a serious, lifelong medical problem. Affected patients have high plasma triglyceride levels (...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Publicado no:J Clin Lipidol
Main Authors: Ashraf, Ambika P., Miyashita, Kazuya, Nakajima, Katsuyuki, Murakami, Masami, Hegele, Robert A., Ploug, Michael, Fong, Loren G., Young, Stephen G., Beigneux, Anne P.
Formato: Artigo
Idioma:Inglês
Publicado em: 2020
Assuntos:
Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7166156/
https://ncbi.nlm.nih.gov/pubmed/32107180
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jacl.2020.01.012
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados