J. C. Bleeker

Disorders of mitochondrial long-chain fatty acid oxidation and the carnitine shuttle

S. Ferdinandusse, R. Wanders, R. Houtkooper, 2018, Reviews in Endocrine and Metabolic Disorders.

Exploring the metabolic fate of medium-chain triglycerides in healthy individuals using a stable isotope tracer.

S. Ferdinandusse, R. Wanders, R. Houtkooper, 2020, Clinical nutrition.

Nutritional ketosis improves exercise metabolism in patients with very long‐chain acyl‐CoA dehydrogenase deficiency

T. Takken, K. Clarke, S. Ferdinandusse, 2020, Journal of inherited metabolic disease.

Electrophysiological Abnormalities in VLCAD Deficient hiPSC-Cardiomyocytes Can Be Improved by Lowering Accumulation of Fatty Acid Oxidation Intermediates

S. Ferdinandusse, R. Wanders, R. Coronel, 2020, International journal of molecular sciences.

Essential Fatty Acid Deficiency in Very Long-Chain Acyl-CoA Dehydrogenase Deficient Patients

R. Wanders, F. Vaz, G. Visser, 2015 .

Severe Fat Accumulation in Multiple Organs in Pediatric Autopsies

S. Ferdinandusse, H. Waterham, P. Nikkels, 2017, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Electrophysiological Abnormalities in VLCAD Deficient hiPSC-Cardiomyocytes Do not Improve with Carnitine Supplementation

S. Ferdinandusse, R. Wanders, R. Houtkooper, 2021, Frontiers in Pharmacology.

Sirtuin activation as a therapeutic approach against inborn errors of metabolism

R. Houtkooper, J. C. Bleeker, 2016, Journal of Inherited Metabolic Disease.

Subclinical effects of long‐chain fatty acid β‐oxidation deficiency on the adult heart: A case‐control magnetic resonance study

S. Ferdinandusse, R. Wanders, A. Nederveen, 2020, Journal of inherited metabolic disease.

Impact of newborn screening for very‐long‐chain acyl‐CoA dehydrogenase deficiency on genetic, enzymatic, and clinical outcomes

S. Ferdinandusse, H. Waterham, R. Wanders, 2019, Journal of inherited metabolic disease.

Proposal for an individualized dietary strategy in patients with very long‐chain acyl‐CoA dehydrogenase deficiency

S. Ferdinandusse, H. Waterham, T. Derks, 2018, Journal of inherited metabolic disease.

Impact of NBS for VLCAD deficiency on genetic, enzymatic and clinical outcomes.

S. Ferdinandusse, H. Waterham, R. Wanders, 2019 .

Proposal for an individualized dietary strategy in patients with very long-chain acyl-CoA dehydrogenase deficiency

S. Ferdinandusse, H. Waterham, T. Derks, 2018, Journal of Inherited Metabolic Disease.

Proposal for an individualized dietary strategy in patients with very long-chain acyl-CoA dehydrogenase deficiency

S. Ferdinandusse, H. Waterham, T. Derks, 2018, Journal of Inherited Metabolic Disease.