The association between a genetic variant in the SULF2 gene, metabolic parameters and vascular disease in patients at high cardiovascular risk

por Heidemann, Britt E, Visseren, Frank LJ, van Setten, Jessica, Marais, A David, Koopal, Charlotte
Publicado 2023

Clinical heterogeneity in monogenic chylomicronaemia

por Heidemann, Britt E, Bemelmans, Remy H H, Marais, A David, Visseren, Frank L J, Koopal, Charlotte
Publicado 2022

Establishing the relationship between familial dysbetalipoproteinemia and genetic variants in the APOE gene

por Heidemann, Britt E., Koopal, Charlotte, Baass, Alexis, Defesche, Joep C., Zuurbier, Linda, Mulder, Monique T., Roeters van Lennep, Jeanine E., Riksen, Niels P., Boot, Christopher, Marais, A. David, Visseren, Frank L. J.
Publicado 2022

Incidence of type 2 diabetes in familial combined hyperlipidemia

por Brouwers, Martijn C G J, de Graaf, Jacqueline, Simons, Nynke, Meex, Steven, ten Doeschate, Sophie, van Heertum, Shadana, Heidemann, Britt, Luijten, Jim, de Boer, Douwe, Schaper, Nicolaas, Stehouwer, Coen D A, van Greevenbroek, Marleen M J
Publicado 2020