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Journal of Inherited Metabolic Disease|December 6, 2019
Hypothesis: determining phenotypic specificity facilitates understanding of pathophysiology in rare genetic disordersHanneke A Haijes, Jaak Jaeken, Peter M van Hasselt
Journal of Medical Genetics|August 30, 2017
Hypothesis: lobe A (COG1-4)-CDG causes a more severe phenotype than lobe B (COG5-8)-CDGHanneke A Haijes, Jaak Jaeken, François Foulquier, et al.
Journal of Inherited Metabolic Disease|October 13, 2019
Glucose transporter type 1 deficiency syndrome and the ketogenic dietMarit Schwantje, Lilly M Verhagen, Peter M van Hasselt, et al.
Nederlands Tijdschrift Voor Geneeskunde|March 6, 2014
[Hereditary fructose intolerance]Lynne Rumping, Hans R Waterham, Irene Kok, et al.
JIMD Reports|January 13, 2023
Isolated neurological presentations of mevalonate kinase deficiencyEva M M Hoytema van Konijnenburg, Esmeralda Oussoren, Joost Frenkel, et al.
Journal of Inherited Metabolic Disease|May 24, 2019
Pathophysiology of propionic and methylmalonic acidemias. Part 2: Treatment strategiesHanneke A Haijes, Peter M van Hasselt, Judith J M Jans, et al.
Molecular Genetics and Metabolism|July 8, 2017
Incomplete biomarker response in mucopolysaccharidosis type I after successful hematopoietic cell transplantationGé-Ann Kuiper, Peter M van Hasselt, Jaap Jan Boelens, et al.
Journal of Inherited Metabolic Disease|June 25, 2020
Hearing loss in patients with mucopolysaccharidoses-1 and -6 after hematopoietic cell transplantation: A longitudinal analysisBrigitte T A van den Broek, Adriana L Smit, Jaap Jan Boelens, et al.
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