Johannes M. Aerts

Leiden, ZH, Netherlands

Last Updated: 09/26/2026

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Found 26 publications

A Contemporary Pathomechanistic Nosology of Inherited Lysosomal Disorders.

A Contemporary Pathomechanistic Nosology of Inherited Lysosomal Disorders.

Journal: Journal of inherited metabolic disease
Published: July 01, 2026

LIMP-2 deficiency-associated glycolipid abnormalities in mice.

LIMP-2 deficiency-associated glycolipid abnormalities in mice.

Journal: Biochimica et biophysica acta. Molecular and cell biology of lipids
Published: April 08, 2025

A multiomic network approach uncovers disease modifying mechanisms of inborn errors of metabolism.

A multiomic network approach uncovers disease modifying mechanisms of inborn errors of metabolism.

Journal: bioRxiv : the preprint server for biology
Published: March 03, 2025

A Multiomic Network Approach to Uncover Disease Modifying Mechanisms of Inborn Errors of Metabolism.

A Multiomic Network Approach to Uncover Disease Modifying Mechanisms of Inborn Errors of Metabolism.

Journal: Journal of inherited metabolic disease
Published: January 12, 2025

Animal Models for the Study of Gaucher Disease.

Animal Models for the Study of Gaucher Disease.

Journal: International journal of molecular sciences
Published: October 09, 2023

Correction: Assessment of plasma lyso-Gb3 for clinical monitoring of treatment response in migalastat-treated patients with Fabry disease.

Correction: Assessment of plasma lyso-Gb3 for clinical monitoring of treatment response in migalastat-treated patients with Fabry disease.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: November 21, 2020

Assessment of plasma lyso-Gb3 for clinical monitoring of treatment response in migalastat-treated patients with Fabry disease.

Assessment of plasma lyso-Gb3 for clinical monitoring of treatment response in migalastat-treated patients with Fabry disease.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: July 08, 2020

An overview of activity-based probes for glycosidases.

An overview of activity-based probes for glycosidases.

Journal: Current opinion in chemical biology
Published: April 25, 2019

Dissociation of globotriaosylceramide and impaired endothelial function in α-galactosidase-A deficient EA.hy926 cells.

Dissociation of globotriaosylceramide and impaired endothelial function in α-galactosidase-A deficient EA.hy926 cells.

Journal: Molecular genetics and metabolism
Published: July 27, 2018

HEPES activates a MiT/TFE-dependent lysosomal-autophagic gene network in cultured cells: A call for caution.

HEPES activates a MiT/TFE-dependent lysosomal-autophagic gene network in cultured cells: A call for caution.

Journal: Autophagy
Published: February 20, 2018

Excessive dietary lipid intake provokes an acquired form of lysosomal lipid storage disease in the kidney.

Excessive dietary lipid intake provokes an acquired form of lysosomal lipid storage disease in the kidney.

Journal: The Journal of pathology
Published: December 16, 2017

Roscoe O. Brady: Physician whose pioneering discoveries in lipid biochemistry revolutionized treatment and understanding of lysosomal diseases.

Roscoe O. Brady: Physician whose pioneering discoveries in lipid biochemistry revolutionized treatment and understanding of lysosomal diseases.

Journal: Blood cells, molecules & diseases
Published: October 17, 2016
Showing 1-12 of 26

Last Updated: 09/26/2026