Projects per year
Personal profile
Research interests
The molecular basis of inherited dyslipidemias and lipid lowering therapies.
Specialisation
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Network
Recent external collaboration on country/territory level. Dive into details by clicking on the dots or
Projects
- 2 Active
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Hovingh G.K.: [NO DATA]
Hovingh, G. K., Bruikman, C. S., van Capelleveen, J. C., Hartgers, M. L., van Iperen, E. P. A., Reeskamp, R. F., Sjouke, B. & Verbeek, R.
1/10/2013 → …
Project: Research
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Stroes E.S.G.: Novel anti-atherogenic strategies targeting the vessel wall
Amraoui, F., Bakker, G. J., van der Bel, R., van den Boogert, M. A. W., Bouter, K. E. C., Bruikman, C. S., van Capelleveen, J. C., Eeftinck Schattenkerk, D. W., Emans, T. W., Gilijamse, P. W., de Groot, P. F., Hartgers, M. L., Hartstra, A. V., Hoogeveen, R. M., Kootte, R. S., Lameijer, M. A., Reeskamp, R. F., Sabry, A. M. R., Sandberg, M., Sjouke, B., Smits, L. P., Stiekema, L. C. A., Surendran, P. P., Udayappan, S. D., Verbeek, R., Verweij, S. L., Zhang, Q., Zheng, K. H. H., Stroes, E. S. G., van den Born, B. H., Dallinga - Thie, G. M., Hovingh, G. K., Kastelein, J. J. P., Mulder, W. J. M., Nederveen, A. J. & Nieuwdorp, M.
1/06/2008 → …
Project: Research
Research output
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Clinical characteristics of primary carnitine deficiency: A structured review using a case-by-case approach
Crefcoeur, L. L., Visser, G., Ferdinandusse, S., Wijburg, F. A., Langeveld, M. & Sjouke, B., 1 May 2022, In: Journal of Inherited Metabolic Disease. 45, 3, p. 386-405 20 p.Research output: Contribution to journal › Review article › Academic › peer-review
Open Access4 Citations (Scopus) -
Patients’ view on gene therapy development for lysosomal storage disorders: a qualitative study
Eskes, E. C. B., Beishuizen, C. R. L., Corazolla, E. M., van Middelaar, T., Brands, M. M. M. G., Dekker, H., van de Mheen, E., Langeveld, M., Hollak, C. E. M. & Sjouke, B., 1 Dec 2022, In: Orphanet Journal of Rare Diseases. 17, 1, 383.Research output: Contribution to journal › Article › Academic › peer-review
Open Access -
Biochemical and imaging parameters in acid sphingomyelinase deficiency: Potential utility as biomarkers
Eskes, E. C. B., Sjouke, B., Vaz, F. M., Goorden, S. M. I., van Kuilenburg, A. B. P., Aerts, J. M. F. G. & Hollak, C. E. M., May 2020, In: Molecular genetics and metabolism. 130, 1, p. 16-26 11 p.Research output: Contribution to journal › Review article › Academic › peer-review
10 Citations (Scopus) -
De juiste zorg op de juiste plek: Een inventarisatie op de poli algemene interne geneeskunde
Sjouke, B., Büller, N. V. J. A., Hoeboer, S., Bont, J. & Geerlings, S. E., Mar 2020, In: Magazine Interne Geneeskinde. p. 24-25 2 p.Research output: Contribution to journal › Article › Professional
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The clinical and molecular diversity of homozygous familial hypercholesterolemia in children: Results from the GeneTics of clinical homozygous hypercholesterolemia (GoTCHA)study
Luirink, I. K., Braamskamp, M. J. A. M., Wiegman, A., Hartgers, M. L., Sjouke, B., Defesche, J. C. & Hovingh, G. K., 2019, In: Journal of clinical lipidology. 13, 2, p. 272-278Research output: Contribution to journal › Article › Academic › peer-review
7 Citations (Scopus)