Plasma levels of PCSK9 and phenotypic variability in familial hypercholesterolemia von Huijgen, R., Fouchier, S.W., Denoun, M., Hutten, B.A., Vissers, M.N., Lambert, G., Kastelein, J.J.P.

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Evaluation of cholesterol lowering treatment of patients with familial hypercholesterolemia: a large cross-sectional study in The Netherlands von Pijlman, A.H, Huijgen, R, Verhagen, S.N, Imholz, B.P.M, Liem, A.H, Kastelein, J.J.P, Abbink, E.J, Stalenhoef, A.F.H, Visseren, F.L.J

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Factor VIII deficiency does not protect against atherosclerosis von BIERE‐RAFI, S., TUINENBURG, A., HAAK, B. W., PETERS, M., HUIJGEN, R., de GROOT, E., VERHAMME, P., PEERLINCK, K., VISSEREN, F. L. J., KRUIP, M. J. H. A., LAROS‐van GORKOM, B. A. P., GERDES, V. E. A., BULLER, H. R., SCHUTGENS, R. E. G., KAMPHUISEN, P. W.

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Venous thrombosis is associated with hyperglycemia at diagnosis: a case–control study von HERMANIDES, J., COHN, D. M., DEVRIES, J. H., KAMPHUISEN, P. W., HUIJGEN, R., MEIJERS, J. C. M., HOEKSTRA, J. B. L., BÜLLER, H. R.

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Real-time MSE measurements for current profile control on KSTAR von De Bock, M F M, Aussems, D, Huijgen, R, Scheffer, M, Chung, J

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Extreme xanthomatosis in patients with both familial hypercholesterolemia and cerebrotendinous xanthomatosis von Huijgen, R, Stork, ADM, Defesche, JC, Peter, J, Alonso, R, Cuevas, A, Kastelein, JJP, Duran, M, Stroes, ESG

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Statins Reduce Hepatic Angptl3 Expression And Secretion, Likely By Interfering With Lxr-Mediated Transcription von Grefhorst, A., Reeskamp, L.F., Huijgen, R., Hovingh, G.K.

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Familial hypercholesterolemia patients with unexplained low ldl-c: a role for angptl3? von Reeskamp, L., Huijgen, R., Grefhorst, A., Hovingh, G.K.

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Founder mutations in the Netherlands: geographical distribution of the most prevalent mutations in the low-density lipoprotein receptor and apolipoprotein B genes von Kusters, D. M., Huijgen, R., Defesche, J. C., Vissers, M. N., Kindt, I., Hutten, B. A., Kastelein, J. J. P.

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Hip surgery sequentially induces stress hyperglycaemia and activates coagulation von HERMANIDES, J, HUIJGEN, R, HENNY, C. P, MOHAMMAD, N. H, HOEKSTRA, J. B. L, LEVI, M, DEVRIES, J. H

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Colesevelam added to combination therapy with a statin and ezetimibe in patients with familial hypercholesterolemia: A 12-week, multicenter, randomized, double-blind, controlled tr... von Huijgen, Roeland, MD, Abbink, Evertine J., MD, PhD, Bruckert, Eric, MD, Stalenhoef, Anton F.H., MD, PhD, FRCP, Imholz, Ben P.M., MD, PhD, Durrington, Paul N., MD, FMedSci, Trip, M.D., MD, PhD, Eriksson, Mats, MD, PhD, Visseren, Frank L.J., MD, PhD, Schaefer, Juergen R., MD, Kastelein, John J.P., MD, PhD

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Real-time MSE measurements for current profile control on KSTARa von De Bock, M. F. M., Aussems, D., Huijgen, R., Scheffer, M., Chung, J.

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Determining When to Add Nonstatin Therapy : A Quantitative Approach von Robinson, JG, Huijgen, R, Ray, KK, Persons, J, Kastelein, JJP, Pencina, MJ

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Abstract: P870 IDENTIFICATION OF APOB AND PCSK9 MUTATIONS CAUSING A NON-ADH PHENOTYPE IN MOLECULAR DIAGNOSED ADH PATIENTS von Fouchier, S, Huijgen, R, Vis, K, Defesche, J, Kastelein, J

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P40 CAROTID ATHEROSCLEROSIS OF PATIENTS WITH FAMILIAL HYPERCHOLESTEROLEMIA NO LONGER DIFFERS FROM UNAFFECTED RELATIVES ALREADY WITHIN 18 MONTHS AFTER IDENTIFICATION von Huijgen, R., Hutten, B.A., Kindt, I., de Groot, E., Kastelein, J.J.P., Vissers, M.N.

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L6 EFFICACY OF 15 YEARS OF GENETIC CASCADE SCREENING FOR FAMILIAL HYPERCHOLESTEROLEMIA IN THE NETHERLANDS IN PREVENTION OF CORONARY ARTERY DISEASE von Huijgen, R., Versmissen, J., Oosterveer, D.M., Kindt, I., Sijbrands, E.J.G., Kastelein, J.J.P.

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603 COMBINING EXOME SEQUENCING WITH EXCLUSION LINKAGE ANALYSIS AS A TOOL TO UNRAVEL THE MOLECULAR BASIS OF A COMMON GENETIC DISEASE von Motazacker, M.M., Huijgen, R., Peter, J., Defesche, J.C., Kastelein, J.J.R, Hovingh, G.K., Kathiresan, S., Zelcer, N., Fouchier, S.W.

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The impact of LDLR function on fibroblast growth factor 21 levels von Besseling, J, Ong, KL, Huijgen, R, Rye, KA, Hovingh, GK, Hutten, BA, Lambert, G

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Abstract: P841 NON-FUNCTIONALITY OF THREE LDL-R AND APOB GENE MUTATIONS THAT WERE ASSUMED TO CAUSE FAMILIAL HYPERCHOLESTEROLEMIA von Huijgen, R, Kindt, I, Fouchier, S, Defesche, J, Hutten, B, Kastelein, J, Vissers, M

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Abstract: 576 LIPID-LOWERING MEDICATION TWO YEARS AFTER MOLECULAR DIAGNOSIS OF FAMILIAL HYPERCHOLESTEROLEMIA von Huijgen, R, Kindt, I, Verhoeven, S, Vissers, M, Kastelein, J, Hutten, B

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