Aerts, Johannes M.

Marked elevation of plasma chitotriosidase activity. A novel hallmark of Gaucher disease.

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Plasma chitotriosidase and CCL18: Early biochemical surrogate markers in type B Niemann‐Pick disease

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Glycoprotein Non-Metastatic Protein B: An Emerging Biomarker for Lysosomal Dysfunction in Macrophages

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Value of plasma chitotriosidase to assess non‐neuronopathic Gaucher disease severity and progression in the era of enzyme replacement therapy

van Dussen, L., Hendriks, E. J., Groener, J. E. M., Boot, R. G., Hollak, C. E. M., & Aerts, J. M. F. G. (2014) · Journal of Inherited Metabolic Disease

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The Unique Phenotype of Lipid-Laden Macrophages

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Patient centered guidelines for the laboratory diagnosis of Gaucher disease type 1

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Plasma chitotriosidase in male Fabry patients: A marker for monitoring lipid-laden macrophages and their correction by enzyme replacement therapy

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Muscle adaptation to short-term fasting in healthy lean humans

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HEPES Activates a MiT/TFE-dependent Lysosomal-Autophagic Gene Network in Cultured Cells: A Call for Caution

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