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Daisy Rymen

Showing results (1-10 of 43) with videos related to

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European Journal of Human Genetics : EJHG|August 1, 2013
Congenital disorders of glycosylation: other causes of ichthyosisJaak Jaeken, Daisy Rymen, Gert Matthijs
Molecular Genetics and Metabolism Reports|June 12, 2025
Adrenal insufficiency in inborn errors of metabolism and vice versa: Case reports and review of the literatureAriane De Preter, Anne Rochtus, Peter Witters, et al.
Molecular Genetics and Metabolism|March 15, 2024
Glycosphingolipids in congenital disorders of glycosylation (CDG)Andrea Jáñez Pedrayes, Daisy Rymen, Bart Ghesquière, et al.
Plos One|May 8, 2025
The use of protein supplements in children with cerebral palsy: A scoping literature reviewIneke Verreydt, Els Ortibus, Anja Van Campenhout, et al.
European Journal of Pediatrics|November 27, 2019
Glycogen storage disease type VI: clinical course and molecular backgroundTim Rj Aeppli, Daisy Rymen, Gabriella Allegri, et al.
Glycoconjugate Journal|September 18, 2012
Approaches to homozygosity mapping and exome sequencing for the identification of novel types of CDGGert Matthijs, Daisy Rymen, María Beatriz Bistué Millón, et al.
Biochemia Medica|October 22, 2024
A case of alkaptonuria presenting with unexplained dark-stained diapers and spurious hyperoxaluria and proteinuria due to homogentisic acid interferenceThibault Vanhove, Margo Aertgeerts, Peter Witters, et al.
Genes|November 17, 2019
Clinical and Molecular Characterization of Classical-Like Ehlers-Danlos Syndrome Due to a Novel <i>TNXB</i> VariantDaisy Rymen, Marco Ritelli, Nicoletta Zoppi, et al.
Genes|November 27, 2021
Genotype-Phenotype Correlations in PMM2-CDGLaurien Vaes, Daisy Rymen, David Cassiman, et al.
Journal of Physical Activity & Health|May 21, 2026
Longitudinal Trajectories of Sedentary Time and Physical Activity in Children With Cerebral Palsy: Time to MoveIneke Verreydt, Olaf Verschuren, Marieke De Craemer, et al.
Pageof 5

Showing results (1-10 of 43) with videos related to

Sort By:
Pageof 5
European Journal of Human Genetics : EJHG|August 1, 2013
Congenital disorders of glycosylation: other causes of ichthyosisJaak Jaeken, Daisy Rymen, Gert Matthijs
Molecular Genetics and Metabolism Reports|June 12, 2025
Adrenal insufficiency in inborn errors of metabolism and vice versa: Case reports and review of the literatureAriane De Preter, Anne Rochtus, Peter Witters, et al.
Molecular Genetics and Metabolism|March 15, 2024
Glycosphingolipids in congenital disorders of glycosylation (CDG)Andrea Jáñez Pedrayes, Daisy Rymen, Bart Ghesquière, et al.
Plos One|May 8, 2025
The use of protein supplements in children with cerebral palsy: A scoping literature reviewIneke Verreydt, Els Ortibus, Anja Van Campenhout, et al.
European Journal of Pediatrics|November 27, 2019
Glycogen storage disease type VI: clinical course and molecular backgroundTim Rj Aeppli, Daisy Rymen, Gabriella Allegri, et al.
Glycoconjugate Journal|September 18, 2012
Approaches to homozygosity mapping and exome sequencing for the identification of novel types of CDGGert Matthijs, Daisy Rymen, María Beatriz Bistué Millón, et al.
Biochemia Medica|October 22, 2024
A case of alkaptonuria presenting with unexplained dark-stained diapers and spurious hyperoxaluria and proteinuria due to homogentisic acid interferenceThibault Vanhove, Margo Aertgeerts, Peter Witters, et al.
Genes|November 17, 2019
Clinical and Molecular Characterization of Classical-Like Ehlers-Danlos Syndrome Due to a Novel <i>TNXB</i> VariantDaisy Rymen, Marco Ritelli, Nicoletta Zoppi, et al.
Genes|November 27, 2021
Genotype-Phenotype Correlations in PMM2-CDGLaurien Vaes, Daisy Rymen, David Cassiman, et al.
Journal of Physical Activity & Health|May 21, 2026
Longitudinal Trajectories of Sedentary Time and Physical Activity in Children With Cerebral Palsy: Time to MoveIneke Verreydt, Olaf Verschuren, Marieke De Craemer, et al.
Pageof 5