Ronald A. Wanders

Amsterdam, NH, Netherlands

Last Updated: 09/26/2026

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Found 205 publications

Molecular and cellular mechanisms underlying gyrate atrophy: Why is the retina primarily affected?

Molecular and cellular mechanisms underlying gyrate atrophy: Why is the retina primarily affected?

Journal: Acta ophthalmologica

Published: November 20, 2024

A Dutch translational knowledge agenda for inherited metabolic diseases.

A Dutch translational knowledge agenda for inherited metabolic diseases.

Journal: Journal of inherited metabolic disease

Published: November 01, 2024

Development of the Dutch translational knowledge agenda for inherited metabolic diseases.

Development of the Dutch translational knowledge agenda for inherited metabolic diseases.

Journal: JIMD reports

Published: September 26, 2024

A mini-review on the international gyrate atrophy symposium 2023: More than meets the eye. Focus on outstanding research questions.

A mini-review on the international gyrate atrophy symposium 2023: More than meets the eye. Focus on outstanding research questions.

Journal: Molecular genetics and metabolism

Published: September 20, 2024

Syndromic retinitis pigmentosa.

Syndromic retinitis pigmentosa.

Journal: Progress in retinal and eye research

Published: July 17, 2024

Docosahexaenoic acid prevents peroxisomal and mitochondrial protein loss in a murine hepatic organoid model of severe malnutrition.

Docosahexaenoic acid prevents peroxisomal and mitochondrial protein loss in a murine hepatic organoid model of severe malnutrition.

Journal: Biochimica et biophysica acta. Molecular basis of disease

Published: June 05, 2024

Extending diagnostic practices in gyrate atrophy: Enzymatic characterization and the development of an in vitro pyridoxine responsiveness assay.

Extending diagnostic practices in gyrate atrophy: Enzymatic characterization and the development of an in vitro pyridoxine responsiveness assay.

Journal: Molecular genetics and metabolism

Published: May 29, 2024

Human glyoxylate metabolism revisited: New insights pointing to multi-organ involvement with implications for siRNA-based therapies in primary hyperoxaluria.

Human glyoxylate metabolism revisited: New insights pointing to multi-organ involvement with implications for siRNA-based therapies in primary hyperoxaluria.

Journal: Journal of inherited metabolic disease

Published: May 24, 2024

Disorders of fatty acid homeostasis.

Disorders of fatty acid homeostasis.

Journal: Journal of inherited metabolic disease

Published: November 15, 2023

Discovery of novel diagnostic biomarkers for Sjögren-Larsson syndrome by untargeted lipidomics.

Discovery of novel diagnostic biomarkers for Sjögren-Larsson syndrome by untargeted lipidomics.

Journal: Biochimica et biophysica acta. Molecular and cell biology of lipids

Published: October 03, 2023

Abnormal activation of MAPKs pathways and inhibition of autophagy in a group of patients with Zellweger spectrum disorders and X-linked adrenoleukodystrophy.

Abnormal activation of MAPKs pathways and inhibition of autophagy in a group of patients with Zellweger spectrum disorders and X-linked adrenoleukodystrophy.

Journal: Orphanet journal of rare diseases

Published: May 29, 2023

Human peroxisomal NAD+/NADH homeostasis is regulated by two independent NAD(H) shuttle systems.

Human peroxisomal NAD+/NADH homeostasis is regulated by two independent NAD(H) shuttle systems.

Journal: Free radical biology & medicine

Published: May 22, 2023

Showing 1-12 of 205

Last Updated: 09/26/2026