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European Journal of Human Genetics : EJHG
|
August 1, 2013
Congenital disorders of glycosylation: other causes of ichthyosis
Jaak 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 literature
Ariane 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 review
Ineke Verreydt, Els Ortibus, Anja Van Campenhout, et al.
European Journal of Pediatrics
|
November 27, 2019
Glycogen storage disease type VI: clinical course and molecular background
Tim 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 CDG
Gert 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 interference
Thibault 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> Variant
Daisy Rymen, Marco Ritelli, Nicoletta Zoppi, et al.
Genes
|
November 27, 2021
Genotype-Phenotype Correlations in PMM2-CDG
Laurien 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 Move
Ineke Verreydt, Olaf Verschuren, Marieke De Craemer, et al.
Page
of 5
Search research articles
Search
Showing results (1-10 of 43) with videos related to
Sort By:
Page
of 5
European Journal of Human Genetics : EJHG
|
August 1, 2013
Congenital disorders of glycosylation: other causes of ichthyosis
Jaak 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 literature
Ariane 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 review
Ineke Verreydt, Els Ortibus, Anja Van Campenhout, et al.
European Journal of Pediatrics
|
November 27, 2019
Glycogen storage disease type VI: clinical course and molecular background
Tim 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 CDG
Gert 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 interference
Thibault 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> Variant
Daisy Rymen, Marco Ritelli, Nicoletta Zoppi, et al.
Genes
|
November 27, 2021
Genotype-Phenotype Correlations in PMM2-CDG
Laurien 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 Move
Ineke Verreydt, Olaf Verschuren, Marieke De Craemer, et al.
Page
of 5