Lodewijk IJlst

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1 Active

Wanders R.J.A.: Focus of research
van de Beek, M., Chatzispyrou, I. A., Daniels, E. G., van Engen, C. E., Falkenberg, K. D., Gao, A., Held, N. M., Herzog, K., Khan, R. R., Schackmann, M. J. A., Liu, J., Wanders, R. J. A., Ferdinandusse, S., Kulik, W., van Roermund, C. W. T., Vaz, F. M., Houtkooper, R., te Brinke, H., Denis, S. W. & IJlst, L.
1/01/2007 → …
Project: Research

125 Article
6 Comment/Letter to the editor
5 Review article

Genetic, biochemical, and clinical spectrum of patients with mitochondrial trifunctional protein deficiency identified after the introduction of newborn screening in the Netherlands
Schwantje, M., Fuchs, S. A., de Boer, L., Bosch, A. M., Cuppen, I., Dekkers, E., Derks, T. G. J., Ferdinandusse, S., Ijlst, L., Houtkooper, R. H., Maase, R., van der Pol, W. L., de Vries, M. C., Verschoof-Puite, R. K., Wanders, R. J. A., Williams, M., Wijburg, F. & Visser, G., 1 Jul 2022, In: Journal of Inherited Metabolic Disease. 45, 4, p. 804-818 15 p.
Research output: Contribution to journal › Article › Academic › peer-review

Open Access

2 Citations (Scopus)
Peroxisomal ATP Uptake Is Provided by Two Adenine Nucleotide Transporters and the ABCD Transporters
van Roermund, C. W. T., IJlst, L., Linka, N., Wanders, R. J. A. & Waterham, H. R., 19 Jan 2022, In: Frontiers in cell and developmental biology. 9, 788921.
Research output: Contribution to journal › Article › Academic › peer-review

Open Access

1 Citation (Scopus)
An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids
Undiagnosed Diseases Network, Apr 2021, In: Genetics in medicine. 23, 4, p. 740-750 11 p.
Research output: Contribution to journal › Article › Academic › peer-review

Open Access

15 Citations (Scopus)
Correction to: An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids (Genetics in Medicine, (2021), 23, 4, (740-750), 10.1038/s41436-020-01027-3)
Undiagnosed Diseases Network, 2021, (E-pub ahead of print) In: Genetics in Medicine.
Research output: Contribution to journal › Comment/Letter to the editor › Academic

Open Access

1 Citation (Scopus)
Electrophysiological Abnormalities in VLCAD Deficient hiPSC-Cardiomyocytes Do not Improve with Carnitine Supplementation
Verkerk, A. O., Knottnerus, S. J. G., Portero, V., Bleeker, J. C., Ferdinandusse, S., Guan, K., IJlst, L., Visser, G., Wanders, R. J. A., Wijburg, F. A., Bezzina, C. R., Mengarelli, I. & Houtkooper, R. H., 12 Jan 2021, In: Frontiers in Pharmacology. 11, 616834.
Research output: Contribution to journal › Article › Academic › peer-review

Open Access

2 Citations (Scopus)

Lodewijk IJlst

Network

Projects

Wanders R.J.A.: Focus of research

Research output

Genetic, biochemical, and clinical spectrum of patients with mitochondrial trifunctional protein deficiency identified after the introduction of newborn screening in the Netherlands

Peroxisomal ATP Uptake Is Provided by Two Adenine Nucleotide Transporters and the ABCD Transporters

An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids

Correction to: An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids (Genetics in Medicine, (2021), 23, 4, (740-750), 10.1038/s41436-020-01027-3)

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