Search Results - "van Olden, C.C."

Proteinuria in early childhood due to familial LCAT deficiency caused by loss of a disulfide bond in lecithin:cholesterol acyl transferase by Holleboom, A.G, Kuivenhoven, J.A, van Olden, C.C, Peter, J, Schimmel, A.W, Levels, J.H, Valentijn, R.M, Vos, P, Defesche, J.C, Kastelein, J.J.P, Hovingh, G.K, Stroes, E.S.G, Hollak, C.E.M

“…Abstract Introduction Familial lecithin:cholesterol acyltransferase (LCAT) deficiency (FLD) is a rare recessive disorder of cholesterol metabolism…”
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Differences in the prevalence of intermediate hyperglycaemia and the associated incidence of type 2 diabetes mellitus by ethnicity: The HELIUS study by van Olden, C.C., Muilwijk, M., Stronks, K., van den Born, B.J., Moll van Charante, E.P., Nicolau, M., Zwinderma, A.H., Nieuwdorp, M., Groen, A.K., van Valkengoed, I.G.M.

“…We aimed to describe differences in the prevalence of intermediate hyperglycaemia (IH) between six ethnic groups. Moreover, to investigate differences in the…”
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