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The Journal of Clinical Investigation|October 1, 1989
A nonsense mutation in the apolipoprotein C-IIPadova gene in a patient with apolipoprotein C-II deficiencyS S Fojo, P Lohse, C Parrott, et al.
American Journal of Physiology. Endocrinology and Metabolism|March 20, 2001
Plasma protein synthesis in patients with low-grade nephrotic proteinuriaM Zanetti, R Barazzoni, G Garibotto, et al.
European Journal of Clinical Investigation|April 1, 1991
Acute effects of HMG-CoA reductase inhibitors on biliary lipids in patients with interrupted enterohepatic circulationM Muraca, G Baggio, L Miconi, et al.
Journal of Lipid Research|October 9, 2001
Phenotypic expression of familial hypobetalipoproteinemia in three kindreds with mutations of apolipoprotein B geneP Tarugi, A Lonardo, C Gabelli, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|September 1, 1996
Homozygous familial hypobetalipoproteinemia. Increased LDL catabolism in hypobetalipoproteinemia due to a truncated apolipoprotein B species, apo B-87PadovaC Gabelli, C Bilato, S Martini, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 14, 2025
Quantification of plasma APOE4 with a novel automated Lumipulse immunoassay enables the identification of homozygous and heterozygous APOE ε4 carrier statusG Musso, C Cosma, S Moz, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|April 16, 1998
Lipoprotein(a) and lipoprotein profile in healthy centenarians: a reappraisal of vascular risk factorsG Baggio, S Donazzan, D Monti, et al.
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