Research output per year
Research output per year
Personal profile
Research interests
Natural history, pathophysiology and treatment of lysosomal storage disorders
Specialisation
Inherited Metabolic Diseases
Network
Recent external collaboration on country/territory level. Dive into details by clicking on the dots or
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Adaptive pathway development for Fabry disease: a clinical approach
Schuller, Y., Arends, M., Körver, S., Langeveld, M. & Hollak, C. E. M., 2018, In: Drug discovery today. 23, 6, p. 1251-1257Research output: Contribution to journal › Article › Academic › peer-review
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Characterization of Classical and Nonclassical Fabry Disease: A Multicenter Study
Arends, M., Wanner, C., Hughes, D., Mehta, A., Oder, D., Watkinson, O. T., Elliott, P. M., Linthorst, G. E., Wijburg, F. A., Biegstraaten, M. & Hollak, C. E., 2017, In: Journal of the American Society of Nephrology. 28, 5, p. 1631-1641Research output: Contribution to journal › Article › Academic › peer-review
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Hyperferritinemia and iron metabolism in Gaucher disease: Potential pathophysiological implications
Regenboog, M., van Kuilenburg, A. B. P., Verheij, J., Swinkels, D. W. & Hollak, C. E. M., 2016, In: Blood reviews. 30, 6, p. 431-437Research output: Contribution to journal › Review article › Academic › peer-review
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The clinical spectrum and pathophysiology of skeletal complications in lysosomal storage disorders
Clarke, L. A. & Hollak, C. E. M., 2015, In: Best practice & research. Clinical endocrinology & metabolism. 29, 2, p. 219-235Research output: Contribution to journal › Article › Academic › peer-review
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Post-authorisation assessment of orphan drugs
Hollak, C. E. M., Biegstraaten, M., Levi, M. & Hagendijk, R., 2015, In: Lancet. 386, 10007, p. 1940-1941Research output: Contribution to journal › Article › Academic › peer-review