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 (...

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Vydáno v:J Clin Lipidol
Hlavní autoři: Ashraf, Ambika P., Miyashita, Kazuya, Nakajima, Katsuyuki, Murakami, Masami, Hegele, Robert A., Ploug, Michael, Fong, Loren G., Young, Stephen G., Beigneux, Anne P.
Médium: Artigo
Jazyk:Inglês
Vydáno: 2020
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Article
On-line přístup: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
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