van Kampen, Antoine H. C.

SGCE isoform characterization and expression in human brain: implications for myoclonus–dystonia pathogenesis?

Ritz, K., van Schaik, B. D., Jakobs, M. E., van Kampen, A. H., Aronica, E., Tijssen, M. A., & Baas, F. (2011) · European Journal of Human Genetics

Deep Brain Stimulation and Movement DisordersGenetic Neurodegenerative Diseases

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Functional characterisation of peroxisomal β‐oxidation disorders in fibroblasts using lipidomics

Herzog, K., Pras‐Raves, M. L., Ferdinandusse, S., Vervaart, M. A. T., Luyf, A. C. M., van Kampen, A. H. C., Wanders, R. J. A., Waterham, H. R., & Vaz, F. M. (2018) · Journal of Inherited Metabolic Disease

Metabolism and Genetic DisordersLipid metabolism and biosynthesis

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Cerebellar and hepatic alterations in ACBD5-deficient mice are associated with unexpected, distinct alterations in cellular lipid homeostasis.

Darwisch, W., von Spangenberg, M., Lehmann, J., Singin, Ö., Deubert, G., Kühl, S., Roos, J., Horstmann, H., Körber, C., Hoppe, S., et al. (2020) · Communications Biology

Metabolism and Genetic DisordersLipid metabolism and biosynthesis

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Multi-Omic Approach to Identify Phenotypic Modifiers Underlying Cerebral Demyelination in X-Linked Adrenoleukodystrophy

Richmond, P. A., van der Kloet, F., Vaz, F. M., Lin, D., Uzozie, A., Graham, E., Kobor, M., Mostafavi, S., Moerland, P. D., Lange, P. F., et al. (2020) · Frontiers in Cell and Developmental Biology

Metabolism and Genetic DisordersLysosomal Storage Disorders Research

Cited by 29