Concepedia

Marit Schwantje

MS

Statistics

Publications

3

Citations

56

H-Index

3

Active since

2019

Affiliations

Wilhelmina Children's Hospital(Current)

University Medical Center Utrecht

Amsterdam University Medical Centers

Emma Kinderziekenhuis

University of Amsterdam

Marit Schwantje is an author at Wilhelmina Children's Hospital specializing in pediatrics, newborn genetic screening, and mitochondrial dysfunction.

ORCID

Publications per year

2019–2024

3

Publications

3

Genetic defect of the sodium‐dependent multivitamin transporter: A treatable disease, mimicking biotinidase deficiency

Marit Schwantje, Monique de Sain‐van der Velden, Judith Jans et al. · JIMD Reports · 2019 · 25 citations · Full text

, , +15

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

Marit Schwantje, Sabine A. Fuchs, Lonneke de Boer et al. · Journal of Inherited Metabolic Disease · 2022 · 19 citations · Full text

, , +16

Tracer‐based lipidomics enables the discovery of disease‐specific candidate biomarkers in mitochondrial β‐oxidation disorders

Marit Schwantje, Signe Mosegaard, Suzan J. G. Knottnerus et al. · The FASEB Journal · 2024 · 12 citations · Full text

, , +16

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