Gepke Visser
5PUBLICATIONS
3CO-AUTHORS
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Publications (5)
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|Oct 07, 2020
Mitochondrial Fatty Acid Oxidation Disorders: Laboratory Diagnosis, Pathogenesis, and the Complicated Route to Treatment.Ronald J A Wanders, Gepke Visser, Sacha Ferdinandusse
|Mar 08, 2020
Conventional and Unconventional Therapeutic Strategies for Sialidosis Type I.Rosario Mosca, Diantha van de Vlekkert, Yvan Campos
|Jan 20, 2020
Nutritional ketosis improves exercise metabolism in patients with very long-chain acyl-CoA dehydrogenase deficiency.Jeannette C Bleeker, Gepke Visser, Kieran Clarke
|Aug 09, 2019
Genetic defect of the sodium-dependent multivitamin transporter: A treatable disease, mimicking biotinidase deficiency.Marit Schwantje, Monique de Sain-van der Velden, Judith Jans
|Feb 15, 2019
Impact of newborn screening for very-long-chain acyl-CoA dehydrogenase deficiency on genetic, enzymatic, and clinical outcomes.Jeannette C Bleeker, Irene L Kok, Sacha Ferdinandusse
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