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The Journal of Clinical Investigation|November 1, 1986
Familial apolipoprotein E deficiencyE J Schaefer, R E Gregg, G Ghiselli, et al.
The American Journal of Cardiology|May 1, 1985
Effects of combination cholestyramine-neomycin treatment on plasma lipoprotein concentrations in type II hyperlipoproteinemiaJ M Hoeg, M B Maher, K R Bailey, et al.
The American Journal of Medicine|September 1, 1983
Massive omental reticuloendothelial cell lipid uptake in Tangier disease after splenectomyE J Schaefer, T J Triche, L A Zech, et al.
Journal of Surgical Oncology|November 1, 1996
Pharmacokinetics of dacarbazine in the regional perfusion of extremities with melanomaM S Didolkar, A J Jackson, L J Lesko, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 15, 1985
Estimation of VLDL cholesterol in hyperlipidemiaP W Wilson, L A Zech, R E Gregg, et al.
The Journal of Clinical Investigation|April 1, 1993
In vivo metabolism of a mutant form of apolipoprotein A-I, apo A-IMilano, associated with familial hypoalphalipoproteinemiaP Roma, R E Gregg, M S Meng, et al.
Journal of Lipid Research|May 11, 1992
In vivo metabolism of a mutant apolipoprotein, apoA-IIowa, associated with hypoalphalipoproteinemia and hereditary systemic amyloidosisD J Rader, R E Gregg, M S Meng, et al.
Journal of Lipid Research|February 1, 1981
Metabolism of high density lipoprotein subfractions and constituents in Tangier disease following the infusion of high density lipoproteinsE J Schaefer, D W Anderson, L A Zech, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|February 1, 1997
Homozygous familial defective apolipoprotein B-100. Enhanced removal of apolipoprotein E-containing VLDLs and decreased production of LDLsJ R Schaefer, H Scharnagl, M W Baumstark, et al.
Journal of Lipid Research|January 1, 1993
Two different allelic mutations in the lecithin:cholesterol acyltransferase (LCAT) gene resulting in classic LCAT deficiency: LCAT (tyr83-->stop) and LCAT (tyr156-->asn)H G Klein, P Lohse, N Duverger, et al.
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