Vascular risk factors, vascular disease, lipids and lipid targets in patients with familial dysbetalipoproteinemia: A European cross-sectional study von Koopal, C, Retterstøl, K, Sjouke, B, Hovingh, G.K, Ros, E, de Graaf, J, Dullaart, R.P.F, Bertolini, S, Visseren, F.L.J

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Thyroid Hormone Mimetics: the Past, Current Status and Future Challenges von Elbers, L.P.B., Kastelein, J.J.P., Sjouke, B.

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Genetic risk score does not explain hypercholesterolaemic phenotype in children with hypercholesterolemia of unknown genetic origin von Sjouke, B, Fouchier, S.W, Wiegman, A, Kastelein, J.J.P, Hovingh, G.K

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Familial Hypercholesterolemia: Present and Future Management von Sjouke, B., Kusters, D. M., Kastelein, J. J. P., Hovingh, G. K.

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Therapy with the thyroid hormone receptor agonist eprotirome in patients with familial hypercholesterolemia: a randomised, double blind, placebo-controlled study von Sjouke, B, Langslet, G, Ceska, R, Nicholls, S.J, Nissen, S.E, Öhlander, M, Ladenson, P.W, Olsson, A.G, Hovingh, G.K, Kastelein, J.J.P

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Long-term tolerance and efficacy of adjunctive exenatide therapy on glycaemic control and bodyweight in type 2 diabetes: a retrospective study from a specialist diabetes outpatient... von Carrington, M. J., Chan, Y.-K., Stewart, S., Sjouke, B., Brazilek, R., Cohen, N.

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Hypercholesterolaemia and hepatosplenomegaly: two manifestations of cholesteryl ester storage disease von Sjouke, B, van der Stappen, J W J, Groener, J E M, Pepping, A, Wevers, R A, Gouw, A, Dikkeschei, L D, Mijnhout, S, Hovingh, G K, Alleman, M A

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Hypercholesterolemia is not necessarily associated with hyperreactive platelets von Korporaal, S.J.A, De Angelis, V, Hoekstra, M, Bochem, A, Sjouke, B, Van Der Sluis, R.J, Hovingh, G.K, Roest, M, Van Eck, M

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Eprotirome in patients with familial hypercholesterolaemia (the AKKA trial): a randomised, double-blind, placebo-controlled phase 3 study von Sjouke, Barbara, MD, Langslet, Gisle, MD, Ceska, Richard, Prof, Nicholls, Stephen J, Prof, Nissen, Steven E, Prof, Öhlander, Maria, MSc, Ladenson, Paul W, Prof, Olsson, Anders G, Prof, Hovingh, G Kees, MD, Kastelein, John J P, Prof

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Double-heterozygous autosomal dominant hypercholesterolemia: Clinical characterization of an underreported disease von Sjouke, B, Defesche, J.C, Hartgers, M.L, Wiegman, A, Roeters van Lennep, J.E, Kastelein, J.J.P, Hovingh, G.K

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Glycoprotein non-metastatic protein B (GPNMB) plasma values in patients with chronic visceral acid sphingomyelinase deficiency von Eskes, E.C.B, Lienden, M.J.C. van der, Sjouke, B., Vliet, L. van, Brands, M.M.M.G., Hollak, C.E.M., Aerts, J.M.F.G.

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Biochemical and imaging parameters in acid sphingomyelinase deficiency: potential utility as biomarkers von Eskes, E.C.B., Sjouke, B., Vaz, F.M., Goorden, S.M.I., Kuilenburg, A.B.P. van, Aerts, J.M.F.G., Hollak, C.E.M.

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The importance of the altricial - precocial spectrum for social complexity in mammals and birds - a review von Scheiber, Isabella B R, Weiß, Brigitte M, Kingma, Sjouke A, Komdeur, Jan

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Patients' view on gene therapy development for lysosomal storage disorders: a qualitative study von Eskes, Eline C B, Beishuizen, Cathrien R L, Corazolla, Eleonore M, van Middelaar, Tessa, Brands, Marion M M G, Dekker, Hanka, van de Mheen, Erica, Langeveld, Mirjam, Hollak, Carla E M, Sjouke, Barbara

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Different diseases, different needs: Patient preferences for gene therapy in lysosomal storage disorders, a probabilistic threshold technique survey von Corazolla, Eleonore M, Eskes, Eline C B, Veldwijk, Jorien, Brands, Marion M M G, Dekker, Hanka, van de Mheen, Erica, Langeveld, Mirjam, Hollak, Carla E M, Sjouke, Barbara

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Nonpharmacological Lipoprotein Apheresis Reduces Arterial Inflammation in Familial Hypercholesterolemia von van Wijk, Diederik F., MD, Sjouke, Barbara, MD, Figueroa, Amparo, MD, Emami, Hamed, MD, van der Valk, Fleur M., MD, MacNabb, Megan H., BA, Hemphill, Linda C., MD, Schulte, Dominik M., MD, PhD, Koopman, Marion G., MD, PhD, Lobatto, Mark E., MD, Verberne, Hein J., MD, PhD, Fayad, Zahi A., MD, PhD, Kastelein, John J.P., MD, PhD, Mulder, Willem J.M., PhD, Hovingh, G. Kees, MD, PhD, Tawakol, Ahmed, MD, Stroes, Erik S.G., MD, PhD

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Attack-defense trees von Kordy, B., Mauw, S., Radomirovic, S., Schweitzer, P.

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Acid sphingomyelinase deficiency and Gaucher disease in adults: Similarities and differences in two macrophage storage disorders von Eskes, Eline C. B., Dussen, Laura, Aerts, Johannes M. F. G., Lienden, Martijn J. C., Maas, Mario, Akkerman, Erik M., Kuilenburg, André B. P., Sjouke, Barbara, Hollak, Carla E. M.

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Natural disease course of chronic visceral acid sphingomyelinase deficiency in adults: A first step toward treatment criteria von Eskes, Eline C B, van Dussen, Laura, Brands, Marion M M G, Vaz, Frédéric M, Aerts, Johannes M F G, van Kuilenburg, André B P, Sjouke, Barbara, Hollak, Carla E M

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Transforming Graphical System Models to Graphical Attack Models von Ivanova, Marieta Georgieva, Probst, Christian W., Hansen, René Rydhof, Kammüller, Florian

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