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Daisy Rymen

Showing results (11-20 of 43) with videos related to

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Clinical Chemistry and Laboratory Medicine|November 29, 2023
Pseudohyperglycemia due to glucometer interference in galactosemiaBram Decru, Hilde Blanckaert, Gunnar Naulaers, et al.
Clinical Nutrition ESPEN|June 12, 2026
Nutritional intake in children with cerebral palsy and typically developing peers: A comprehensive study using a novel smartphone applicationIneke Verreydt, Daisy Rymen, Lauraine Staut, et al.
Molecular Genetics and Metabolism|January 11, 2025
Mitochondrial HMG-CoA synthase deficiencyBram Decru, Marine Lys, Kobe Truijens, et al.
The Journal of Dermatology|June 26, 2024
Quality of life in children with erythropoietic protoporphyria: a case-control studyLouisa G Kluijver, Debby Wensink, Margreet A E M Wagenmakers, et al.
Journal of Anatomy|July 25, 2025
Medial gastrocnemius and semitendinosus muscle growth in typically developing children: Longitudinal reference growth trajectoriesIneke Verreydt, Ines Vandekerckhove, Geert Molenberghs, et al.
Molecular Metabolism|June 30, 2022
Pyruvate and uridine rescue the metabolic profile of OXPHOS dysfunctionIsabelle Adant, Matthew Bird, Bram Decru, et al.
Proteomics. Clinical Applications|October 25, 2023
"Hide and seek": Misleading transferrin variants in PMM2-CDG complicate diagnosticsAlexandre Raynor, Arnaud Bruneel, Pieter Vermeersch, et al.
Orphanet Journal of Rare Diseases|December 12, 2012
COG5-CDG: expanding the clinical spectrumDaisy Rymen, Liesbeth Keldermans, Valérie Race, et al.
JIMD Reports|March 17, 2021
SLC37A4-CDG: Second patientMatthew P Wilson, Dulce Quelhas, Elisa Leão-Teles, et al.
Human Molecular Genetics|March 9, 2022
CAMLG-CDG: a novel congenital disorder of glycosylation linked to defective membrane traffickingMatthew P Wilson, Zoé Durin, Özlem Unal, et al.
Pageof 5

Showing results (11-20 of 43) with videos related to

Sort By:
Pageof 5
Clinical Chemistry and Laboratory Medicine|November 29, 2023
Pseudohyperglycemia due to glucometer interference in galactosemiaBram Decru, Hilde Blanckaert, Gunnar Naulaers, et al.
Clinical Nutrition ESPEN|June 12, 2026
Nutritional intake in children with cerebral palsy and typically developing peers: A comprehensive study using a novel smartphone applicationIneke Verreydt, Daisy Rymen, Lauraine Staut, et al.
Molecular Genetics and Metabolism|January 11, 2025
Mitochondrial HMG-CoA synthase deficiencyBram Decru, Marine Lys, Kobe Truijens, et al.
The Journal of Dermatology|June 26, 2024
Quality of life in children with erythropoietic protoporphyria: a case-control studyLouisa G Kluijver, Debby Wensink, Margreet A E M Wagenmakers, et al.
Journal of Anatomy|July 25, 2025
Medial gastrocnemius and semitendinosus muscle growth in typically developing children: Longitudinal reference growth trajectoriesIneke Verreydt, Ines Vandekerckhove, Geert Molenberghs, et al.
Molecular Metabolism|June 30, 2022
Pyruvate and uridine rescue the metabolic profile of OXPHOS dysfunctionIsabelle Adant, Matthew Bird, Bram Decru, et al.
Proteomics. Clinical Applications|October 25, 2023
"Hide and seek": Misleading transferrin variants in PMM2-CDG complicate diagnosticsAlexandre Raynor, Arnaud Bruneel, Pieter Vermeersch, et al.
Orphanet Journal of Rare Diseases|December 12, 2012
COG5-CDG: expanding the clinical spectrumDaisy Rymen, Liesbeth Keldermans, Valérie Race, et al.
JIMD Reports|March 17, 2021
SLC37A4-CDG: Second patientMatthew P Wilson, Dulce Quelhas, Elisa Leão-Teles, et al.
Human Molecular Genetics|March 9, 2022
CAMLG-CDG: a novel congenital disorder of glycosylation linked to defective membrane traffickingMatthew P Wilson, Zoé Durin, Özlem Unal, et al.
Pageof 5