T W de Bruin

Impaired fatty acid metabolism in familial combined hyperlipidemia. A mechanism associating hepatic apolipoprotein B overproduction and insulin resistance.

M. Castro Cabezas, T W de Bruin, Harold W. de Valk et al. · Journal of Clinical Investigation · 1993 · 201 citations · Full text

Nutrition, Hyperlipidemia, Fch Phenotype +22

Impaired chylomicron remnant clearance in familial combined hyperlipidemia.

M. Castro Cabezas, T W de Bruin, Hans Jansen et al. · Arteriosclerosis and Thrombosis A Journal of Vascular Biology · 1993 · 127 citations · Full text

Complex genetic contribution of the Apo AI-CIII-AIV gene cluster to familial combined hyperlipidemia. Identification of different susceptibility haplotypes.

Geesje M. Dallinga‐Thie, M van Linde-Sibenius Trip, Jerome I. Rotter et al. · Journal of Clinical Investigation · 1997 · 112 citations · Full text

Different Susceptibility Haplotypes, Genetics, Genetic Epidemiology +22

Lipoprotein(a) and apolipoprotein B plasma concentrations in hypothyroid, euthyroid, and hyperthyroid subjects.

T W de Bruin, H van Barlingen, M van Linde-Sibenius Trip et al. · The Journal of Clinical Endocrinology & Metabolism · 1993 · 110 citations

Thyroid Status, Hyperlipidemia, Metabolic Syndrome +20

Apolipoprotein A-I/C-III/A-IV gene cluster in familial combined hyperlipidemia: effects on LDL-cholesterol and apolipoproteins B and C-III.

Geesje M. Dallinga‐Thie, Xingyao Bu, M van Linde-Sibenius Trip et al. · Journal of Lipid Research · 1996 · 106 citations · Full text